259 results on '"Martin, M. R."'
Search Results
102. ChemInform Abstract: PSEUDOESTERS AND DERIVATIVES. PART 20. ACID-CATALYZED REACTIONS OF 5-METHOXYFURAN-2(5H)-ONE WITH THIOLS
- Author
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FARINA, F., primary, MARTIN, M. R., additional, and PARELLADA, M. D., additional
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- 1984
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103. Determination of the Surface Geometry for the Aluminum (110) and (111) Surfaces by Comparison of Low-Energy-Electron-Diffraction Calculations with Experiment
- Author
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Martin, M. R., primary and Somorjai, G. A., additional
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- 1973
- Full Text
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104. Kinetics of Synthesis and Rate of Degradation of T Antigen Induced by Polyoma Virus
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Nicoli, J., primary, Meyer, G., additional, and Martin, M.-R., additional
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- 1971
- Full Text
- View/download PDF
105. Instrumental Neutron Activation Analyses of Lunar Specimens
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Golescaron, G. G., primary, Osawa, M., additional, Randle, K., additional, Beyer, R. L., additional, Jerome, D. Y., additional, Lindstrom, D. J., additional, Martin, M. R., additional, McKay, S. M., additional, and Steinborn, T. L., additional
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- 1970
- Full Text
- View/download PDF
106. ChemInform Abstract: (SS)-5-Ethoxy-3-p-Tolylsulfinylfuran-2(5H)-ones as Chiral Dipolarophiles: First Asymmetric Cycloaddition of Diazomethane to Vinyl Sulfoxides.
- Author
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GARCIA RUANO, J. L., FRAILE, A., and MARTIN, M. R.
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- 1996
- Full Text
- View/download PDF
107. Is this a record? Six years in "Paris".
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Martin, M R, Hardwick, P, and Killick, A
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- 1999
- Full Text
- View/download PDF
108. Prevalence and risk factors for delirium in critically ill patients with COVID-19 (COVID-D): a multicentre cohort study
- Author
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Ana Vallejo de la Cueva, Pablo T. Aznar, Laura González Cubillo, Chiara Robba, Oriol Plans Galván, Nerea Aretxabala Cortajarena, Robert C. Hyzy, Imen Ben Saida, Jorge Rubio, María José Sánchez Carretero, Katie M. Vance, Blanca Furquet, Irene Patricia Barón Barrera, Sarah J. Peterson, Sara C. LaHue, Sergio Llorente Damas, Andrew R. Vogel, Nihal Patel, Alejandro Suarez-de-la-Rica, Cristina Álvarez, Ricard Molina Latorre, Günseli Orhun, Karen Shephard, Marta Martín Martínez, Paula Castello-Mora, Guillem Navarra-Ventura, Michelle Woodham, Carmen Andrea Sanchis-Veryser, Annachiara Marra, Kristine Nelson, Carolina Ferrer Gómez, Francisco Javier Morán Gallego, Muhammed Elhadi, Sarah Cohen, María Esther Rodriguez Delgado, Rafael Badenes, Isabel Reyes García, Christopher Berkey, Karla Núñez Vázquez, Beata-Gabriela K Simpson, Amaia Quintano Rodero, María Pilar Vicente-Fernández, María Luisa García Pérez, Vanja C. Douglas, María Elena Martínez Quintana, Silvia García de Castrillón i Ramal, Silvia Beretta, Mandeep Sing, Robert A Balk, Yolanda Poveda Hernández, Spencer Roberson, Martin Siegemund, Jordi Morillas Pérez, Rameela Raman, Giuseppe Servillo, João Manoel Silva, Brenda T. Pun, Aurélien Mazeraud, María Cruz Martín Delgado, Borja Hinojal Olmedillo, Gemma Gomà Fernández, Miguel Valente, Michael T. Kenes, Laura Galarza, Fabio Silvio Taccone, Wencong Chen, Rita Pereia, Álvaro Ortega Guerrero, Morgan H. Tandy, Alejandro Ruiz Perea, Stephanie Wilson-Linville, Meri Martin Cerezuela, Salvatore Lucio Cutuli, Carlos A. Calvo, María de las Nieves Noci Moreno, Ariadna Bellès, Elisa Govea Bogossian, Mario Dalorzo González, Eva Álvarez Torres, David Díaz Muñoz, Carla Margarida Teixeira, Emilio del Campo Molina, Sol Fernandez-Gonzalo, Christine Harb, Berta Monleón, Anna Teresa Mazzeo, Beatriz Del Moral Barbudo, Thomas Godet, Cristina Delgado Palacios, C. Adrian Austin, Hilde Wøien, Anselmo Caricato, Erik Roman-Pognuz, Bruno Gonçalves, Patricia Rodríguez Villamizar, Eloisa Sofia Tanzarella, Daniel A Godoy Torres, Robert E. Hosse, Lisa Smit, María Rosa Sanchis-Martin, Cristina Murcia Gubianas, Emily Sanders, Karen Herrera-Davis, Sara Torrico Sánchez, Isabel Peña Luna, David A Bennett, Irene Torres, Diana Gil-Castillejos, Laura Labrador Romero, Felipe González-Seguel, Carlos Muñoz De Cabo, Ellis Morgan, Itziar Insausti, Mónica García Simón, Patricia Piñeiro Otero, Genís Carrasco Gómez, M. Montero, Jose García Cantos, Ignacio Garutti, César Rodriguez Nuñez, Fernando Higuero, Sameep Sehgal, Catherine M. Kuza, Yago García Blanco-Traba, Juan Romeu Prieto, Ainhoa Serrano, Elena Abril Palomares, Perihan Ergin Özcan, Mathieu van der Jagt, Elena Gallego Curto, Berta Gallego Rodríguez, Rosalía Navarro Casado, Aaron Lerner, Myrto Tzimou, Sheila Moya Gutiérrez, Beatriz García Góngora, Eleonora Stival, Xavier Andorrà Sunyer, Susana Gallardo Sánchez, Anna Baró Serra, Filadelfo Bustos Molina, Rafael Zaragoza, Verónica Rojas, Paolo Pelosi, Aris Pérez Lucendo, Stéphane Legriel, Eduardo Tobar, Laura Lizama, Viviane Hidalgo-Calibin, Chiara Maria Concetta Massaro, Nekane Romero, Pablo García Domelo, Isabel Jesus Pereira, Kelly Drumright, Frank Rasulo, Mattia Marchesi, Jacques Creteur, Estefanía Carvajal Revuelta, Timothy D. Girard, Pablo Carreño-Montenegro, Ana Montero Feijoo, Ignacio Baeza Gómez, Alba Gonzalo Millán, Esteban Morcillo, Alice Santos, Pilar Leal Sanz, Dulce Morales, Gabriel Heras La Calle, Hollis R. O’Neal, Antonio Ramírez-Palma, Inés Pérez Francisco, Alberto Noto, Matilde González Serrano, Paola Valls, María Jesús Mármol Cubillo, Emilio Maseda, Anna Estermann, Andrés Pujol, E. Wesley Ely, Alexis Ferré, Lucia Chowdhury, Guillaume Lacave, Cristina Granja, Isabel de la Calle Gil, Onur M Orun, Mohamed Boussarsar, David Pestaña Lagunas, Denise Battaglini, Nathan E. Brummel, Rosa María Pérez Manrique, Núria Zellweger, Jaume Puig, Kiran Devulapally, Milagros Calizaya Vargas, Jesús Caballero, Theresa Olasveengen, Cristina Fuster, Aarti Sarwal, Pratik P. Pandharipande, Gabriele Pintaudi, Paula Ramirez, Blanca Fernández Tomás, Maria Claudia Giménez Santamarina, Francisco Luis Pérez Caballero, Enver Rodriguez-Martinez, David Martínez-Gascueña, Irene Paredes Borrachero, Ugo Fraisse, Paloma LaTorre Andreu, Ignacio Catalán-Monzón, Elena Gonzalez, Figen Esen, Lorenzo Peluso, Intensive Care, Pun, B. T., Badenes, R., Heras La Calle, G., Orun, O. M., Chen, W., Raman, R., Simpson, B. -G. K., Wilson-Linville, S., Hinojal Olmedillo, B., Vallejo de la Cueva, A., van der Jagt, M., Navarro Casado, R., Leal Sanz, P., Orhun, G., Ferrer Gomez, C., Nunez Vazquez, K., Pineiro Otero, P., Taccone, F. S., Gallego Curto, E., Caricato, A., Woien, H., Lacave, G., O'Neal, H. R., Peterson, S. J., Brummel, N. E., Girard, T. D., Ely, E. W., Pandharipande, P. P., Creteur, J., Bogossian, E. G., Peluso, L., Gonzalez-Seguel, F., Hidalgo-Cabalin, V., Carreno-Montenegro, P., Rojas, V., Tobar, E., Ramirez-Palma, A., Herrera-Davis, K., Ferre, A., Legriel, S., Godet, T., Fraisse, U., Goncalves, B., Mazeraud, A., Tzimou, M., Rasulo, F., Beretta, S., Marchesi, M., Robba, C., Battaglini, D., Pelosi, P., Mazzeo, A. T., Noto, A., Servillo, G., Marra, A., Cutuli, S. L., Pintaudi, G., Stival, E., Tanzarella, E. S., Roman-Pognuz, E., Concetta Massaro, C. M., Elhadi, M., Smit, L., Olasveengen, T., Pereira, I. J., Teixeira, C. M., Santos, A., Valente, M., Granja, C., Pereia, R., Silva, J., Furquet, B., Garcia Simon, M., Godoy Torres, D. A., Monleon, B., Morcillo, E., Romero, N., Serrano, A., Torrico Sanchez, S., Perez Caballero, F. L., Pena Luna, I., Baeza Gomez, I., Calizaya Vargas, M., Morillas Perez, J., Carrasco Gomez, G., Molina Latorre, R., Moya Gutierrez, S., Baron Barrera, I. P., Delgado Palacios, C., Garcia Gongora, B., Labrador Romero, L., Galarza, L., Catalan-Monzon, I., Rodriguez-Martinez, E., Murcia Gubianas, C., Belles, A., Rodriguez Delgado, M. E., Caballero, J., Morales, D., Pujol, A., Rubio, J., Alvarez Torres, E., Carvajal Revuelta, E., de la Calle Gil, I., Fernandez Tomas, B., Gallego Rodriguez, B., Gonzalez Serrano, M., LaTorre Andreu, P., Perez Lucendo, A., Abril Palomares, E., Gonzalez Gonzalez, E., Martin Delgado, M. C., Munoz De Cabo, C., Aznar, P. T., Calvo, C. A., Garutti, I., Higuero, F., Martinez-Gascuena, D., Maseda, E., Insausti, I., Montero Feijoo, A., Suarez-de-la-Rica, A., Del Moral Barbudo, B., Garcia Blanco-Traba, Y., Gimenez Santamarina, M. C., Gonzalo Millan, A., Llorente Damas, S., Pestana Lagunas, D., Reyes Garcia, I., Ruiz Perea, A., Ortega Guerrero, A., Marmol Cubillo, M. J., Diaz Munoz, D., Garcia de Castrillon i Ramal, S., Andorra Sunyer, X., Noci Moreno, M. D. L. N., Perez Manrique, R. M., del Campo Molina, E., Martinez Quintana, M. E., Fernandez-Gonzalo, S., Goma Fernandez, G., Navarra-Ventura, G., Baro Serra, A., Fuster, C., Plans Galvan, O., Gil-Castillejos, D., Dalorzo Gonzalez, M., Moran Gallego, F. J., Paredes Borrachero, I., Rodriguez Villamizar, P., Romeu Prieto, J., Sanchez Carretero, M. J., Gallardo Sanchez, S., Bustos Molina, F., Garcia Perez, M. L., Castello-Mora, P., Puig, J., Sanchis-Martin, M. R., Sanchis-Veryser, C. A., Vicente-Fernandez, M. P., Zaragoza, R., Lizama, L., Torres, I., Alvarez, C., Ramirez, P., Martin Cerezuela, M., Montero, M. J., Garcia Cantos, J., Valls, P., Aretxabala Cortajarena, N., Garcia Domelo, P., Gonzalez Cubillo, L., Martin Martinez, M., Perez Francisco, I., Poveda Hernandez, Y., Quintano Rodero, A., Rodriguez Nunez, C., Siegemund, M., Estermann, A., Zellweger, N., Ben Saida, I., Boussarsar, M., Esen, F., Ergin Ozcan, P., Berkey, C., Harb, C., Tandy, M. H., Morgan, E., Shephard, K., Hyzy, R. C., Kenes, M., Nelson, K., Hosse, R. E., Vance, K. M., Austin, C. A., Lerner, A., Sanders, E., Balk, R. A., Bennett, D. A., Vogel, A. R., Chowdhury, L., Devulapally, K., Woodham, M., Cohen, S., Patel, N., Kuza, C. M., Sing, M., Roberson, S., Drumright, K., Sehgal, S., Lahue, S. C., Douglas, V. C., and Sarwal, A.
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Pulmonary and Respiratory Medicine ,medicine.medical_specialty ,medicine.medical_treatment ,covid-19 ,delirium ,Outcomes ,Lower risk ,Critical Ilness ,Task-Force ,03 medical and health sciences ,0302 clinical medicine ,SDG 3 - Good Health and Well-being ,Intensive-Care-Unit ,Intensive care ,Settore MED/41 - ANESTESIOLOGIA ,medicine ,Survivors ,030212 general & internal medicine ,Simplified Acute Physiology Score ,Mechaniically Ventilated Patients ,Epitiomology ,Mechanical ventilation ,Coma ,Intensive-Care-Unit, Mechaniically Ventilated Patients, Clinical practice Guidelines, Critical Ilness, Task-Force, Sedation, ICU, Survivors, Outcomes, Epitiomology ,business.industry ,covid ,Retrospective cohort study ,Articles ,Clinical practice Guidelines ,covid, delirium ,030228 respiratory system ,Sedation ,ICU ,Emergency medicine ,Delirium ,medicine.symptom ,business ,Cohort study - Abstract
Background: To date, 750 000 patients with COVID-19 worldwide have required mechanical ventilation and thus are at high risk of acute brain dysfunction (coma and delirium). We aimed to investigate the prevalence of delirium and coma, and risk factors for delirium in critically ill patients with COVID-19, to aid the development of strategies to mitigate delirium and associated sequelae. Methods: This multicentre cohort study included 69 adult intensive care units (ICUs), across 14 countries. We included all patients (aged ≥18 years) admitted to participating ICUs with severe acute respiratory syndrome coronavirus 2 infection before April 28, 2020. Patients who were moribund or had life-support measures withdrawn within 24 h of ICU admission, prisoners, patients with pre-existing mental illness, neurodegenerative disorders, congenital or acquired brain damage, hepatic coma, drug overdose, suicide attempt, or those who were blind or deaf were excluded. We collected de-identified data from electronic health records on patient demographics, delirium and coma assessments, and management strategies for a 21-day period. Additional data on ventilator support, ICU length of stay, and vital status was collected for a 28-day period. The primary outcome was to determine the prevalence of delirium and coma and to investigate any associated risk factors associated with development of delirium the next day. We also investigated predictors of number of days alive without delirium or coma. These outcomes were investigated using multivariable regression. Findings: Between Jan 20 and April 28, 2020, 4530 patients with COVID-19 were admitted to 69 ICUs, of whom 2088 patients were included in the study cohort. The median age of patients was 64 years (IQR 54 to 71) with a median Simplified Acute Physiology Score (SAPS) II of 40·0 (30·0 to 53·0). 1397 (66·9%) of 2088 patients were invasively mechanically ventilated on the day of ICU admission and 1827 (87·5%) were invasively mechanical ventilated at some point during hospitalisation. Infusion with sedatives while on mechanical ventilation was common: 1337 (64·0%) of 2088 patients were given benzodiazepines for a median of 7·0 days (4·0 to 12·0) and 1481 (70·9%) were given propofol for a median of 7·0 days (4·0 to 11·0). Median Richmond Agitation–Sedation Scale score while on invasive mechanical ventilation was –4 (–5 to –3). 1704 (81·6%) of 2088 patients were comatose for a median of 10·0 days (6·0 to 15·0) and 1147 (54·9%) were delirious for a median of 3·0 days (2·0 to 6·0). Mechanical ventilation, use of restraints, and benzodiazepine, opioid, and vasopressor infusions, and antipsychotics were each associated with a higher risk of delirium the next day (all p≤0·04), whereas family visitation (in person or virtual) was associated with a lower risk of delirium (p
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- 2021
109. Trends and outcome of neoadjuvant treatment for rectal cancer: A retrospective analysis and critical assessment of a 10-year prospective national registry on behalf of the Spanish Rectal Cancer Project
- Author
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Gianluca Pellino, Rafael Alós, Sebastiano Biondo, Antonio Codina-Cazador, José María Enríquez-Navascues, Eloy Espín-Basany, José Vicente Roig-Vila, Andrés Cervantes, Eduardo García-Granero, Raúl Adell Carceller, Juan Guillermo Ais Conde, Evelio Alonso Alonso, Antonio Amaya Cortijo, Antonio Arroyo Sebastian, Pedro Barra Baños, Ricard Batlle Solé, Juan C. Bernal Sprekelsen, Francisco J. Blanco Gonzalez, Santiago Blanco, J. Bollo, Nieves Cáceres Alvarado, Ignasi Camps Ausas, Ramon Cantero Cid, José Antonio Carmona Saez, Enrique Casal Nuñez, Luis Cristobal Capitán Morales, Guillermo Carreño Villarreal, Jesús Cifuentes Tebar, Miguel Á. Ciga Lozano, Antonio Codina Cazador, Juan de Dios Franco Osorio, María de la Vega Olías, Mario de Miguel Velasco, Sergio Rodrigo del Valle, José G. Díaz Mejías, José M. Díaz Pavón, Javier Die Trill, José L. Dominguez Tristancho, Paula Dujovne Lindenbaum, José Errasti Alustiza, Alejandro Espí Macias, Eloy Espín Basany, Rafael Estévan Estévan, Alfredo M. Estevez Diz, Luis Flores, Domenico Fraccalvieri, Alessandro Garcea, Mauricio García Alonso, Miguel Garcia Botella, Maria José García Coret, Alfonso García Fadrique, José M. García García, Jacinto García García, Jesús Á. Garijo Alvarez, José Gomez Barbadillo, Fernando Gris, Verónica Gumbau, Javier Gutierrez, Pilar Hernandez Casanovas, Daniel Huerga Alvarez, Ana M. Huidobro Piriz, Francisco Javier Jimenez Miramón, Ana Lage Laredo, Alberto Lamiquiz Vallejo, Félix Lluis Casajuana, Manuel López Lara, Juan A. Lujan Mompean, María Victoria Maestre, Eva Martí Martínez, M. Martinez, Javier Martinez Alegre, Gabriel Martínez Gallego, Roberto Martinez Pardavila, Olga Maseda Díaz, Mónica Millan Schedling, Benito Mirón, José Monzón Abad, José A. Múgica Martinera, Francisco Olivet Pujol, Mónica Orelogio Orozco, Luis Ortiz de Zarate, Rosana Palasí Gimenez, Natividad Palencia García, Pablo Palma Carazo, Alberto Parajo Calvo, Jesús Paredes Cotore, Carlos Pastor Idoate, Miguel Pera Roman, Francisco Pérez Benítez, José A. Pérez García, Marta Piñol Pascual, Isabel Prieto Nieto, Ricardo Rada Morgades, Mónica Reig Pérez, Ángel Reina Duarte, Didac Ribé Serrat, Xavier Rodamilans, María D. Ruiz Carmona, Marcos Rodriguez Martin, Francisco Romero Aceituno, Jesús Salas Martínez, Ginés Sánchez de la Villa, Inmaculada Segura Jimenez, José Enrique Sierra Grañon, Amparo Solana Bueno, Albert Sueiras Gil, Teresa Torres Sanchez, Natalia Uribe Quintana, Javier Valdés Hernández, Fancesc Vallribera, Vicent Viciano Pascual, Pellino, G., Alos, R., Biondo, S., Codina-Cazador, A., Enriquez-Navascues, J. M., Espin-Basany, E., Roig-Vila, J. V., Cervantes, A., Garcia-Granero, E., Carceller, R. A., Ais Conde, J. G., Alonso, E. A., Cortijo, A. A., Sebastian, A. A., Banos, P. B., Sole, R. B., Bernal Sprekelsen, J. C., Blanco Gonzalez, F. J., Blanco, S., Bollo, J., Alvarado, N. C., Ausas, I. C., Cid, R. C., Carmona Saez, J. A., Nunez, E. C., Capitan Morales, L. C., Villarreal, G. C., Tebar, J. C., Ciga Lozano, M. A., Cazador, A. C., de Dios Franco Osorio, J., Olias, M. D. L. V., de Miguel Velasco, M., Rodrigo del Valle, S., Diaz Mejias, J. G., Diaz Pavon, J. M., Trill, J. D., Dominguez Tristancho, J. L., Lindenbaum, P. D., Alustiza, J. E., Macias, A. E., Basany, E. E., Estevan, R. E., Estevez Diz, A. M., Flores, L., Fraccalvieri, D., Garcea, A., Alonso, M. G., Botella, M. G., Garcia Coret, M. J., Fadrique, A. G., Garcia Garcia, J. M., Garcia, J. G., Garijo Alvarez, J. A., Barbadillo, J. G., Gris, F., Gumbau, V., Gutierrez, J., Casanovas, P. H., Alvarez, D. H., Huidobro Piriz, A. M., Jimenez Miramon, F. J., Laredo, A. L., Vallejo, A. L., Casajuana, F. L., Lara, M. L., Lujan Mompean, J. A., Maestre, M. V., Martinez, E. M., Martinez, M., Alegre, J. M., Gallego, G. M., Pardavila, R. M., Diaz, O. M., Schedling, M. M., Miron, B., Abad, J. M., Mugica Martinera, J. A., Pujol, F. O., Orozco, M. O., Ortiz de Zarate, L., Gimenez, R. P., Garcia, N. P., Carazo, P. P., Calvo, A. P., Cotore, J. P., Idoate, C. P., Roman, M. P., Benitez, F. P., Perez Garcia, J. A., Pascual, M. P., Nieto, I. P., Morgades, R. R., Perez, M. R., Duarte, A. R., Serrat, D. R., Rodamilans, X., Ruiz Carmona, M. D., Martin, M. R., Aceituno, F. R., Martinez, J. S., Sanchez de la Villa, G., Jimenez, I. S., Sierra Granon, J. E., Bueno, A. S., Gil, A. S., Sanchez, T. T., Quintana, N. U., Hernandez, J. V., Vallribera, F., and Pascual, V. V.
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Male ,Survival ,Colorectal cancer ,medicine.medical_treatment ,T stage ,030230 surgery ,TNM ,0302 clinical medicine ,Registries ,Stage (cooking) ,Rectal cancer ,Aged, 80 and over ,Margins of Excision ,General Medicine ,Middle Aged ,Neoadjuvant Therapy ,Survival Rate ,medicine.anatomical_structure ,Treatment Outcome ,Oncology ,030220 oncology & carcinogenesis ,Female ,Adult ,medicine.medical_specialty ,Neoadjuvant treatment ,Prognosi ,Rectum ,03 medical and health sciences ,Young Adult ,medicine ,Adjuvant therapy ,Humans ,Chemotherapy ,Aged ,Neoplasm Staging ,Retrospective Studies ,Radiotherapy ,business.industry ,Rectal Neoplasms ,Cancer ,Chemoradiotherapy, Adjuvant ,medicine.disease ,Surgery ,Radiation therapy ,Spain ,T-stage ,business ,Follow-Up Studies ,Forecasting - Abstract
Introduction: Preoperative treatment and adequate surgery increase local control in rectal cancer. However, modalities and indications for neoadjuvant treatment may be controversial. Aim of this study was to assess the trends of preoperative treatment and outcomes in patients with rectal cancer included in the Rectal Cancer Registry of the Spanish Associations of Surgeons. Method: This is a STROBE-compliant retrospective analysis of a prospective database. All patients operated on with curative intention included in the Rectal Cancer Registry were included. Analyses were performed to compare the use of neoadjuvant/adjuvant treatment in three timeframes: I)2006–2009; II)2010–2013; III)2014–2017. Survival analyses were run for 3-year survival in timeframes I-II. Results: Out of 14, 391 patients, 8871 (61.6%) received neoadjuvant treatment. Long-course chemo/radiotherapy was the most used approach (79.9%), followed by short-course radiotherapy ± chemotherapy (7.6%). The use of neoadjuvant treatment for cancer of the upper third (15-11 cm) increased over time (31.5%vs 34.5%vs 38.6%, p = 0.0018). The complete regression rate slightly increased over time (15.6% vs 16% vs 18.5%; p = 0.0093); the proportion of patients with involved circumferential resection margins (CRM) went down from 8.2% to 7.3%and 5.5% (p = 0.0004). Neoadjuvant treatment significantly decreased positive CRM in lower third tumors (OR 0.71, 0.59–0.87, Cochrane-Mantel-Haenszel P = 0.0008). Most ypN0 patients also received adjuvant therapy. In MR-defined stage III patients, preoperative treatment was associated with significantly longer local-recurrence-free survival (p < 0.0001), and cancer-specific survival (p < 0.0001). The survival benefit was smaller in upper third cancers. Conclusion: There was an increasing trend and a potential overuse of neoadjuvant treatment in cancer of the upper rectum. Most ypN0 patients received postoperative treatment. Involvement of CRM in lower third tumors was reduced after neoadjuvant treatment. Stage III and MRcN + benefited the most.
- Published
- 2020
110. Observations of Modified Three-Dimensional Instability Structure for Imploding z -Pinch Liners that are Premagnetized with an Axial Field.
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Awe, T. J., McBride, R. D., Jennings, C. A., Lamppa, D. C., Martin, M. R., Rovang, D. C., Slutz, S. A., Cuneo, M. E., Owen, A. C., Sinars, D. B., Tomlinson, K., Gomez, M. R., Hansen, S. B., Herrmann, M. C., McKenney, J. L., Nakhleh, C., Robertson, G. K., Rochau, G. A., Savage, M. E., and Schroen, D. G.
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Z-pinch , *MAGNETIZATION , *HELICAL structure , *MAGNETOHYDRODYNAMICS , *THREE-dimensional display systems - Abstract
Novel experimental data are reported that reveal helical instability formation on imploding z-pinch liners that are premagnetized with an axial field. Such instabilities differ dramatically from the mostly azimuthally symmetric instabilities that form on unmagnetized liners. The helical structure persists at nearly constant pitch as the liner implodes. This is surprising since, at the liner surface, the azimuthal drive field presumably dwarfs the axial field for all but the earliest stages of the experiment. These fundamentally 3D results provide a unique and challenging test for 3D-magnetohydrodynamics simulations. [ABSTRACT FROM AUTHOR]
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- 2013
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111. A self-assembling split aptamer multiplex assay for SARS-COVID19 and miniaturization of a malachite green DNA-based aptamer.
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R O'Steen M and M Kolpashchikov D
- Abstract
Multiplex assays often rely on expensive sensors incorporating covalently linked fluorescent dyes. Herein, we developed a self-assembling aptamer-based multiplex assay. This multiplex approach utilizes a previously established split aptamer sensor in conjugation with a novel split aptamer sensor based upon a malachite green DNA aptamer. This system was capable of simultaneous fluorescent detection of two SARS COVID-19-related sequences in one sample with individual sensors that possesses a limit of detection (LOD) in the low nM range. Optimization of the Split Malachite Green (SMG) sensor yielded a minimized aptamer construct, Mini-MG, capable of inducing fluorescence of malachite green in both a DNA hairpin and sensor format., Competing Interests: The authors declare no conflict of interests., (© 2022 The Authors. Published by Elsevier B.V.)
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- 2022
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112. [Executive summary of the guidelines on the diagnosis and treatment of acute heart failure].
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Nieminen MS, Böhm M, R Cowie M, Drexler H, Filippatos GS, Jondeau G, Hasin Y, Lopez-Sendon J, Mebazaa A, Metra M, Rhodes A, and Swedberg K
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- Acute Disease, Algorithms, Heart Failure etiology, Humans, Heart Failure diagnosis, Heart Failure therapy
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- 2005
113. Dohnavur Fellowship--an experience of dentistry in south India.
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Martin MR
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- Fellowships and Scholarships, Health Services Needs and Demand, India, Medically Underserved Area, Dental Health Services, Religious Missions
- Published
- 1993
114. Identifying Hispanic gifted children using the Screening Assessment for Gifted Elementary Students.
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Tallent-Runnels MK and Martin MR
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- Child, Female, Humans, Male, Psychometrics, Texas, Aptitude Tests statistics & numerical data, Child, Gifted psychology, Hispanic or Latino psychology
- Abstract
We examined the utility of the Screening Assessment for Gifted Elementary Students (SAGES) for identifying Hispanic gifted students among 162 third through fifth graders, of whom 75% were Anglo-American and 25% Hispanic. Direct discriminant analysis of subscale scores of the SAGES classified 93.2% of the sample as Anglo-American, including 35 of the 41 Hispanic children. This indicated that the subscale scores did not predict group membership. A validation procedure yielded similar results on an independent sample of 25 Anglo-American and 14 Hispanic children. Also, a multivariate profile analysis indicated small score differences between the two groups and reflected similar cognitive processes being assessed. The screening device appears to function fairly within both ethnic groups.
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- 1992
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115. An overview of tumor biology.
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Freeman CS, Martin MR, and Marks CL
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- Animals, Female, Humans, Male, Neoplasm Metastasis, Neoplasms etiology, Neoplasms genetics
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- 1990
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116. Maternal deaths in South Australia 1970 to 1975.
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Martin MR
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- Abortion, Spontaneous mortality, Australia, Female, Humans, Obstetric Labor Complications mortality, Pregnancy, Pregnancy Complications mortality, Retrospective Studies, Maternal Mortality
- Abstract
During the period from 1970 to 1975 there were 128 087 confinements in South Australia and 30 maternal deaths were reported, representing a maternal mortality rate of 23 per 100 000 confinements which is lower than in previous reports. Twenty-one deaths were directly due to complications of pregnancy and childbirth, and nine were due to associated conditions. The fall in the maternal mortality rate was largely due to a reduction in the number of deaths from abortion and in the number of confinements to women in the higher-risk older age groups. Infection appeared for the first time as a major cause of maternal death. Avoidable factors may have contributed to 47% of the deaths.
- Published
- 1979
- Full Text
- View/download PDF
117. Structure-activity relations of excitatory amino acids on frog and rat spinal neurones.
- Author
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Biscoe TJ, Evans RH, Headley PM, Martin MR, and Watkins JC
- Subjects
- Amino Acids, Sulfur pharmacology, Animals, Anthelmintics pharmacology, In Vitro Techniques, Rats, Structure-Activity Relationship, Amino Acids pharmacology, Neurons drug effects, Spinal Cord cytology
- Abstract
1 A series of compounds structurally related to glutamic acid has been tested on frog and rat spinal neurones. The substances were added to procaine-containing medium bathing the isolated hemiscected spinal cord of the frog, and their potencies in depolarizing motoneurones were assessed by the magnitude of the potential produced in the ventral root. The electrophoretic technique was used to administer the substances around single interneurones of the rat spinal cord and the relative potencies of the compounds as excitants assessed by the magnitude of the currents required to produce similar rates of neuronal firing. 2 Parallel structure-activity relations were observed in the two series of experiments, suggesting that the receptors for excitatory amino acids on frog and rat spinal neurones are similar. 3 Quisqualate, domoate and kainate were the strongest excitants in both animals, with potencies around two orders of magnitude higher than that of L-glutamate. 4 2,4,5-Trihydroxyphenylalanine (6-OH-DOPA) was a stronger excitant and L-3,4-dihydroxyphenylalanine (L-dopa) a weaker excotamt than L-glutamate on frog spinal motoneurones. The former compounds was also a more potent convulsant than L-glutamate on intraventricular injection into mouse brain. The lack of activity of 6-OH-DOPA on electrophoretic administration was attributed to oxidation. 5 Unlike the majority of amino acid excitants, several of the compounds shown in the present work to have moderate excitatory activity are not anionic at physiological pH. This indicates either that two negatively charged groups are not essential for interaction with a common excitatory receptor, or that more than one type of receptor is involved in the actions demonstrated.
- Published
- 1976
- Full Text
- View/download PDF
118. Morphology of the cochlear nucleus of the normal and reeler mutant mouse.
- Author
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Martin MR
- Subjects
- Animals, Cochlear Nerve cytology, Mice, Mice, Neurologic Mutants, Species Specificity, Staining and Labeling, Cochlear Nerve anatomy & histology
- Abstract
The morphology of the cochlear nuclei of normal and reeler mutant mice were studied in Nissl-stained sections. The cochlear nucleus in both mice is divisible into three parts: the anteroventral, posteroventral, and dorsal nuclei. Nine cell types can be recognized in the normal mouse. In the anteroventral nucleus spherical cells occupy the rostral pole. Globular cells are located caudally and extend to the interstitial region of the anteroventral nucleus. In the posteroventral nucleus multipolar cells are located rostrally and dark-staining cells occupy the caudal pole. Multipolar cells are also present in the anteroventral nucleus and in the deep region and molecular layer of the dorsal cochlear nucleus. The dorsal and lateral aspects of the ventral nuclei are covered by a granule cell layer. The dorsal nucleus consists of superficial molecular and pyramidal layers and a deep region. The deep region contains small and giant cells as well as multipolar cells. The pyramidal layer is made up of pyramidal cells, horizontal cells, and granule cells. Small cells are also present in the molecular layer and throughout the ventral nuclei. The dorsal cochlear nucleus of the reeler mutant mouse is disorganized and the molecular layer is reduced in thickness. The organization of the pyramidal layer is disrupted with granule cells superficial to pyramidal and horizontal cells. Cells which appear to be homologous to pyramidal cells are also present in the deep region of the dorsal nucleus. The total number of granule cells is reduced by an average of 42% over the whole nucleus and the reduction in granule cells is greatest in the granule cell cap covering the dorsal and lateral surface of the ventral cochlear nuclei. The cytoarchitecture of the ventral cochlear nucleus appears normal.
- Published
- 1981
- Full Text
- View/download PDF
119. Treatment of unstable detrusor (irritable bladder) using fluphenazine and nortriptyline: progress report.
- Author
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Martin MR and James ED
- Subjects
- Clinical Trials as Topic, Double-Blind Method, Drug Combinations, Female, Humans, Male, Urinary Bladder Diseases complications, Urination Disorders etiology, Fluphenazine administration & dosage, Nortriptyline administration & dosage, Urinary Bladder Diseases drug therapy, Urination Disorders drug therapy
- Published
- 1981
120. Sideroblastic anaemia in association with malignant histiocytosis.
- Author
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Prentice RL, Bain BJ, and Martin MR
- Subjects
- Aged, Anemia, Sideroblastic pathology, Bone Marrow pathology, Female, Histiocytes pathology, Humans, Lung Neoplasms pathology, Lymph Nodes pathology, Lymphatic Diseases pathology, Anemia, Sideroblastic complications, Lung Neoplasms complications, Lymphatic Diseases complications
- Abstract
A 69-year-old women died of malignant histiocytosis in association with sideroblastic anaemia. Respiratory insufficiency was a prominent clinical feature and was found to be due to obstruction of pulmonary capillaries by malignant histiocytes. It is possible that the same abnormal myeloid clone gave rise to malignant histiocytosis and sideroblastic anaemia.
- Published
- 1981
- Full Text
- View/download PDF
121. Depression of synaptic excitation and of amino acid induced excitatory responses of spinal neurones by D-alpha-aminoadipate, alpha,epsilon-diaminopimelic acid and HA-966.
- Author
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Biscoe TJ, Davies J, Dray A, Evans RH, Francis AA, Martin MR, and Watkins JC
- Subjects
- Animals, Anura, Depression, Chemical, In Vitro Techniques, Rats, 2-Aminoadipic Acid pharmacology, Amino Acids pharmacology, Amino Acids, Dicarboxylic pharmacology, Diaminopimelic Acid pharmacology, Neurons drug effects, Pimelic Acids pharmacology, Pyrrolidinones pharmacology, Spinal Cord cytology, Synapses drug effects
- Published
- 1977
- Full Text
- View/download PDF
122. Comparison of the effects of bicuculline and strychnine on brain stem auditory evoked potentials in the cat.
- Author
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Martin MR and Penix LP
- Subjects
- Animals, Cats, Electrophysiology, Female, Male, Time Factors, Bicuculline pharmacology, Brain Stem drug effects, Evoked Potentials, Auditory drug effects, Strychnine pharmacology
- Abstract
1 Experiments were performed to determine the effects of intravenously applied bicuculline and strychnine on the click-evoked brain stem auditory evoked potentials (BAEP) of cats. 2 The BAEP was not affected by bicuculline (0.5 mg/kg, i.v.) administration. Strychnine (0.2 mg/kg, i.v.) administration caused a significant increase in the amplitude of peak 4, which is thought to be produced by potentials in the superior olive, lateral lemniscus and inferior colliculus. 3 These results suggest that strychnine blocks glycinergic inhibitory inputs to these auditory structures.
- Published
- 1983
- Full Text
- View/download PDF
123. An overview of tumor biology.
- Author
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Freeman CS, Kimes BW, Martin MR, and Marks CL
- Subjects
- Animals, Animals, Genetically Modified, Cell Differentiation, Cell Division, DNA-Binding Proteins physiology, GTP-Binding Proteins physiology, Gene Amplification, Humans, Oncogenes, Translocation, Genetic, Neoplasms physiopathology
- Published
- 1989
- Full Text
- View/download PDF
124. Effects of D,L-alpha-aminoadipate on postsynaptic amino acid responses in cultured mouse spinal cord neurons.
- Author
-
Bergey GK, Martin MR, and Hermes M
- Subjects
- Animals, Aspartic Acid pharmacology, Culture Techniques, Evoked Potentials drug effects, Glutamates pharmacology, Glycine pharmacology, Mice, Synaptic Transmission drug effects, gamma-Aminobutyric Acid pharmacology, 2-Aminoadipic Acid pharmacology, Amino Acids pharmacology, Amino Acids, Dicarboxylic pharmacology, Spinal Cord drug effects, Synapses drug effects
- Abstract
The effects of the dicarboxylic amino acid, DL-alpha-aminoadipate (DLAA) on amino acid responses have been investigated using intracellular recordings from mouse spinal cord neurons grown in dissociated cell culture. DL-alpha-Aminoadipate markedly antagonized postsynaptic responses to iontophoretically appllied aspartate; antagonism of glutamate was much less prominent. DL-alpha-Aminoadipate altered the affinity of aspartate for its receptor while having no observed effects on aspartate-receptor cooperativity. No direct effects of DLAA on membrane potentials or passive membrane properties were seen at the currents used for antagonism. Responses to the inhibitory amino acids GABA and glycine were unaffected by DLAA.
- Published
- 1980
- Full Text
- View/download PDF
125. Neglected coeliac disease.
- Author
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McCrae WM, Eastwood MA, Martin MR, and Sircus W
- Subjects
- Adolescent, Adult, Anemia etiology, Blood Proteins analysis, Body Constitution, Celiac Disease blood, Celiac Disease complications, Celiac Disease pathology, Child, Female, Folic Acid blood, Follow-Up Studies, Glutens, Hemoglobins analysis, Humans, Intestinal Neoplasms etiology, Iron blood, Jejunum pathology, Magnesium blood, Male, Vitamin B 12 blood, Celiac Disease diagnosis, Intestinal Neoplasms diagnosis, Lymphoma diagnosis, Precancerous Conditions diagnosis
- Abstract
A review has been carried out of patients diagnosed as having coeliac disease some years previously and subsequently lost to follow-up. Most were unaware of the need for continuing treatment and had returned to a normal diet. The resulting morbidity was slight, although one patient had died of a small-bowel lymphoma. If untreated coeliac disease is indeed a pre-malignant condition, then it is suggested that there must be a large population at risk, with no motivation to return to treatment other than the risk of malignancy itself.
- Published
- 1975
- Full Text
- View/download PDF
126. The effects of iontophoretically applied antagonists on auditory nerve and amino acid evoked excitation of anteroventral cochlear nucleus neurons.
- Author
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Martin MR
- Subjects
- 2-Aminoadipic Acid pharmacology, Animals, Aspartic Acid pharmacology, Cats, Female, Glutamates pharmacology, Iontophoresis, Magnesium pharmacology, Male, Amino Acids pharmacology, Cochlea drug effects, Neurons drug effects, Vestibulocochlear Nerve physiology
- Published
- 1980
- Full Text
- View/download PDF
127. Evidence for an excitatory amino acid as the transmitter of the auditory nerve in the in vitro mouse cochlear nucleus.
- Author
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Martin MR
- Subjects
- 2-Amino-5-phosphonovalerate, 2-Aminoadipic Acid pharmacology, Action Potentials drug effects, Animals, Aspartic Acid analogs & derivatives, Aspartic Acid pharmacology, Dose-Response Relationship, Drug, Evoked Potentials drug effects, Female, Kainic Acid pharmacology, Male, Mice, Mice, Inbred C3H, N-Methylaspartate, Oxadiazoles pharmacology, Pipecolic Acids pharmacology, Quisqualic Acid, Receptors, Neurotransmitter drug effects, Valine analogs & derivatives, Valine pharmacology, Amino Acids physiology, Cochlear Nerve physiology, Neurotransmitter Agents physiology, Receptors, Neurotransmitter physiology, Vestibulocochlear Nerve physiology
- Abstract
Microionophoretically applied excitatory amino acids induced firing of extracellularly recorded single units in a tissue slice preparation of the mouse cochlear nucleus, and the similarly applied antagonist 2-amino-5-phosphonovalerate (2APV) was demonstrated to be a selective N-methyl-D-aspartate (NMDA) receptor antagonist. In addition, the effect of various bath-applied excitatory amino acid receptor antagonists on auditory nerve evoked field potentials was studied. Antagonists which block NMDA type receptors, blocked auditory nerve evoked potentials in a dose-dependent manner. The 50% effective concentration (EC50) for three of the antagonists used was: D-alpha-aminoadipate, 7.8 mM; 2APV, 4.2 mM; and 2,3-cis-piperidine dicarboxylate, 1.1 mM. Glutamate diethylester (5 mM) had no effect. The results suggest that NMDA, kainate and quisqualate receptors are present in the cochlear nucleus and that auditory nerve transmission in the mouse is mediated by an NMDA type receptor. This is consistent with the concept that the auditory nerve postsynaptic receptor in mammals is of the NMDA type.
- Published
- 1985
- Full Text
- View/download PDF
128. Early detection of meconium-stained liquor during labor: a contribution to fetal care.
- Author
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Matthews CD and Martin MR
- Subjects
- Abruptio Placentae epidemiology, Acidosis diagnosis, Apgar Score, Female, Fetal Death epidemiology, Fetoscopy, Humans, Hydrogen-Ion Concentration, Infant Mortality, Infant, Newborn, Labor, Induced, Obstetric Labor Complications epidemiology, Placenta, Pregnancy, Pregnancy, Prolonged, Umbilical Cord, Amniotic Fluid analysis, Fetal Diseases diagnosis, Labor, Obstetric, Meconium
- Published
- 1974
- Full Text
- View/download PDF
129. The identification of mossy fibres and their cells of origin in the normal and Lurcher mutant mouse.
- Author
-
Caddy KW, Martin MR, and Biscoe TJ
- Subjects
- Animals, Cerebellar Cortex physiopathology, Electric Stimulation, Evoked Potentials, Mice, Mice, Inbred C3H, Movement Disorders physiopathology, Mutation, Neural Pathways, Spinal Cord physiopathology, Cerebellum ultrastructure, Gait, Movement Disorders pathology
- Abstract
The behavioural mutant mouse Lurcher survives to adult life as the heterozygote (Lc/+) and shows a disorder of gait. The neurological lesion has been shown to involve degeneration of Purkinje cells and inferior olivary neurones (Caddy and Biscoe 1976). It follows that the climbing fibre input is reduced and we wished to know if the mossy fibre input was also affected. Heterozygote Lurcher mutants were compared with the wild type in all experiments. Mossy fibre glomeruli were identified in the cerebellum of the mutant mouse by electron microscopy. Horseradish peroxidase (HRP) was injected into the cerebellum and was found in the cells of Clarke's column in the spinal cord. Electrophysiological experiments showed that following stimulation of the sciatic nerve evoked responses could be recorded in the cerebellum. It is concluded that the mossy fibre input to the cerebellum is intact in the Lurcher mutant mouse.
- Published
- 1977
- Full Text
- View/download PDF
130. Histogenesis of the cochlear nucleus of the mouse.
- Author
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Martin MR and Rickets C
- Subjects
- Aging, Animals, Autoradiography, Cochlear Nerve embryology, Cochlear Nerve growth & development, Embryo, Mammalian, Female, Gestational Age, Mice, Pregnancy, Thymidine metabolism, Cochlear Nerve cytology
- Abstract
In Nissl-stained preparations of the cochlear nucleus there are nine recognizable cell types. These cells are born during three periods of histogenesis prenatally. On gestation days 10.0, 10.5, and 11.0 the pyramidal, giant, and dark-staining cells are born. The spherical, globular, multipolar, and horizontal cells are formed on gestation days 12.0, 12.5, and 13.0 and small cells follow on gestation day 14.5. The onset of granule cell formation is gestation day 14.5 continues to birth on gestation day 19. At birth, and for at least the first 2 postnatal weeks, glial cells are born. There are no regional gradients in cell birth dates, cells from all birth dates being intermixed. Cell birth proceeds in an orderly sequence that is related only to cell size. Although there were no apparent spatiotemporal patterns, some clustering of labeled cells was evident. These observations do not support the hypothesis that Golgi Type I cells precede Golgi Type II cells in their order of birth since both large and small neurons project beyond the nucleus. There is, nonetheless, a sequential pattern in the onset of cell birth for the auditory system, with cochlear nucleus neurons preceding cochlear neurons.
- Published
- 1981
- Full Text
- View/download PDF
131. A concentric multi-barrelled micro-electrode for use in microiontophoresis [proceedings].
- Author
-
Biscoe TJ, Martin MR, and Rickets C
- Subjects
- Electrophysiology instrumentation, Iontophoresis instrumentation, Microelectrodes
- Published
- 1978
132. Numbers and diameters of motoneurons and myelinated axons in the facial nucleus and nerve of the albino rat.
- Author
-
Martin MR, Caddy KW, and Biscoe TJ
- Subjects
- Animals, Axons ultrastructure, Cell Count, Male, Rats, Facial Nerve ultrastructure, Motor Neurons ultrastructure, Nerve Fibers, Myelinated ultrastructure, Pons ultrastructure
- Abstract
The number and diameter of the motoneurons in serial sections of the facial nucleus in the albino rat were estimated using a photograph-camera lucida technique for counting and measuring cells in conjunction with a systematic section method for sampling the population. The mean diameter of facial motoneuron nucleoli was also estimated. Total cell counts were estimated using two formulas, one a basic count and the other the basic count corrected for split nucleoli errors. The mean motoneuron diameter is 33-93 micronm (+/- 6-18 micronm S.D.). The number and diameter of myelinated axons in both the facial nerve and its cutaneous auricular branch at the level of the stylomastoid foramen were estimated. There are 5353 myelinated axons in the facial nerve, with a mean diameter of 2-74 micronm, and 627 myelinated axons in the cutaneous auricular branch with a mean diameter of 1-47 micronm. The accuracy and reproductibility of results using the photograph-camera lucida technique for counting and measuring cells and the systematic section method of sampling are compared with those of the methods used by previous investigators. The accuracy of results obtained for estimates of the total cell count using the formulas for the basic count and the basic count corrected for split nucleoli are also compared.
- Published
- 1977
133. Naloxone and long term potentiation of hippocampal CA3 field potentials in vitro.
- Author
-
Martin MR
- Subjects
- Animals, Female, Guinea Pigs, Hippocampus drug effects, Membrane Potentials drug effects, Pyramidal Tracts drug effects, Hippocampus physiology, Naloxone pharmacology, Pyramidal Tracts physiology
- Abstract
The effects of naloxone on potentiation of CA3 pyramidal cell field potentials induced by tetanization of the mossy fiber pathway was studied in the in vitro guinea pig hippocampal slice preparation. Naloxone in nanomolar concentrations prevented the development of long term potentiation and it is concluded that an opioid peptide is probably involved in the generation of the potentiation.
- Published
- 1983
- Full Text
- View/download PDF
134. Electrophysiological observations on the spinal cord of the normal and dystrophic mouse.
- Author
-
Biscoe TJ, Headley PM, Martin MR, and Stirling CA
- Subjects
- Afferent Pathways physiopathology, Animals, Evoked Potentials, Mice, Muscular Dystrophy, Animal pathology, Myelin Sheath pathology, Neural Conduction, Neural Inhibition, Reaction Time, Reflex, Spinal Nerve Roots pathology, Spinal Nerve Roots physiopathology, Muscular Dystrophy, Animal physiopathology, Spinal Cord physiopathology
- Abstract
A method of carrying out electrophysiological experiments on the mouse spinal cord is described. The conduction velocity in the spinal dorsal roots (DR) of the normal mouse was in the range 10-100 m sec-1 and in the ventral roots (VR) 50-70 m sec-1. In the dystrophic mutant (129 ReJ dy/dy) the conduction velocity for both roots was usually in the range 0.1-2.0 m sec-1. Reflexes from DR to VR were recorded in both mutant and wild type animals and it was concluded that the delays in the mutant reflex were probably due to the slower conduction velocity in the roots. Postsynaptic inhibition and presynaptic inhibition were demonstrated and records were made from Renshaw cells and intracellularly from motoneurones. Delayed activity in spinal reflex paths, probably of supraspinal origin, was more pronounced in the dystrophic mutant. It is concluded that if the dystrophic mouse mutant were to be regarded as a model for human disease then similar reflex delays should be demonstrated in human subjects with muscular dystrophy.
- Published
- 1977
- Full Text
- View/download PDF
135. D-alpha-aminoadipate, alpha, epsilon-diominopimelic acid and HA-966 as antagonists of amino acid-induced and synpatic excitation of mammalian spinal neurones in vivo.
- Author
-
Biscoe TJ, Davies J, Dray A, Evans RH, Martin MR, and Watkins JC
- Subjects
- Acetylcholine antagonists & inhibitors, Animals, Aspartic Acid antagonists & inhibitors, Cats, Evoked Potentials drug effects, Excitatory Amino Acid Antagonists, Ganglia, Spinal drug effects, Interneurons drug effects, Kainic Acid antagonists & inhibitors, Mice, Mice, Inbred C3H, Motor Neurons drug effects, Synapses drug effects, 2-Aminoadipic Acid pharmacology, Amino Acids, Dicarboxylic pharmacology, Diaminopimelic Acid pharmacology, Pimelic Acids pharmacology, Pyrrolidinones pharmacology, Spinal Cord drug effects, Synaptic Transmission drug effects
- Published
- 1978
- Full Text
- View/download PDF
136. Physiological studies on facial reflexes in the rat.
- Author
-
Martin MR and Biscoe TJ
- Subjects
- Action Potentials, Animals, Electric Stimulation, Male, Motor Neurons physiology, Neural Pathways, Rats, Reflex, Synaptic Transmission, Facial Nerve physiology, Glossopharyngeal Nerve physiology, Hypoglossal Nerve physiology, Lingual Nerve physiology, Mandibular Nerve physiology
- Abstract
Experiments were performed on 36 male albino rats anaesthetized with pentobarbitone sodium and paralyzed with gallamine triethiodide. Recordings were made with single and multibarrel glass microelectrodes in the facial nucleus and monopolar silver wire electrodes on the lingual, facial, glossopharyngeal and hypoglossal nerves. The absolute refractory period for facial motoneurones is 2-3 ms, the relative refractory period has a duration of 26-34 ms and the range in axonal conduction velocities is from 15 to 45 m.sec-1. No evidence for afferent fibres in the muscle branches of the facial and hypoglassal nerves could be found. The lingual and glossopharyngeal nerves show reflex connexions with both the facial and hypoglassal nerves. The time courses of the potentiations and depressions of test facial antidromic field potentials following lingual and glossopharyngeal conditioning stimuli are given. Evoked synaptic activity and the distribution of field potentials in the facial mucleus following lingual and glossopharyngeal nerve stimulation are also described. The observed lingual and glossopharyngeal-facial reflexes are discussed with respect to blink reflexes.
- Published
- 1977
- Full Text
- View/download PDF
137. Morphology of the facial nucleus of the rat.
- Author
-
Martin MR and Lodge D
- Subjects
- Animals, Brain Mapping, Evoked Potentials, Facial Nerve physiology, Female, Motor Neurons, Pons physiology, Rats, Facial Nerve anatomy & histology, Pons anatomy & histology
- Abstract
The facial nucleus of the rat can be divided into 5 morphological subdivisions. Using a method for the correlation of the observed subdivisions with antidromic field profiles, the orgins of the major muscle branches of the facial nerve in the motor nucleus were determined. The posterior auricular branch is in the medial, the cervical in the ventromedial, the inferior and superior buccolabiales in the lateral, the zygomatic in the dorsal and the temporal and digastric in the intermediate subdivision. The results are consistent with an organization of the motor nucleus reflecting a corresponding topographic organization of the facial musculature.
- Published
- 1977
- Full Text
- View/download PDF
138. Incidence of renomedullary interstitial cell tumours and correlation with hypertension.
- Author
-
Martin MR and Tiltman AJ
- Subjects
- Adolescent, Adult, Age Factors, Aged, Child, Female, Fibroma complications, Humans, Kidney Medulla, Kidney Neoplasms complications, Male, Middle Aged, Sex Factors, Fibroma epidemiology, Hypertension complications, Kidney Neoplasms epidemiology
- Abstract
In a study of 223 consecutive autopsies of subjects older tumours were found in 36 cases (16%) (25/130 males and 11/93 females). Only eight kidneys showed multiple lesions. Renomedullary interstitial cell tumours were correlated with the presence or absence of hypertension and no statistically significant correlation could be demonstrated. The incidence of renomedullary interstitial cell tumours increases with age.
- Published
- 1976
139. The sensitivity of rat spinal interneurones and renshaw cells to L-glutamate and L-aspartate.
- Author
-
Biscoe TJ, Headley PM, Lodge D, Martin MR, and Watkins JC
- Subjects
- Action Potentials drug effects, Animals, Male, Rats, Spinal Cord cytology, Aspartic Acid pharmacology, Glutamates pharmacology, Interneurons drug effects, Spinal Cord drug effects
- Abstract
L-Glutamate and L-aspartate were administered electrophoretically near spinal interneurones and Renshaw cells of pentobarbitone-annaesthetized rats. Other spinal interneurones were consistently more sensitive to L-glutamate than to L-aspartate. Renshaw cells, however, showed no consistent difference in their sensitivity to these two amino acids. The results, which are compared with those reported previously in the cat, support the hypothesis that L-glutamate could be a transmitter at spinal primary afferent terminals.
- Published
- 1976
- Full Text
- View/download PDF
140. Lack of effect of DL-alpha-aminoadipate, an excitatory amino acid antagonist, on cat auditory nerve responses to sound.
- Author
-
Fex J and Martin MR
- Subjects
- Animals, Cats, Evoked Potentials, Auditory drug effects, Hair Cells, Auditory drug effects, 2-Aminoadipic Acid pharmacology, Amino Acids, Dicarboxylic pharmacology, Cochlea drug effects, Vestibulocochlear Nerve drug effects
- Published
- 1980
- Full Text
- View/download PDF
141. Pharmacological studies of facial motoneurones in the rat.
- Author
-
Martin MR, Lodge D, Headley PM, and Biscoe TJ
- Subjects
- Action Potentials drug effects, Animals, Aspartic Acid analogs & derivatives, Aspartic Acid pharmacology, Bicuculline pharmacology, Drug Interactions, Glossopharyngeal Nerve drug effects, Glutamates pharmacology, Homocysteine pharmacology, Lingual Nerve drug effects, Lingual Nerve physiology, Male, Motor Neurons physiology, Pyrrolidines pharmacology, Rats, Refractory Period, Electrophysiological drug effects, Strychnine pharmacology, Face innervation, Motor Neurons drug effects
- Abstract
Experiments were performed on 39 male albino rats anaesthetized with pentobarbitone sodium and paralyzed with gallamine triethiodide. Facial motoneurones consistently showed a progressive alteration of spike shape and decrease in spike firing frequency during the continuous microelectrophoretic application of the excitant amino acids D,L-homocysteate, L-glutamate, L-aspartate, and kainate, but infrequently during that of N-methyl-D-aspartate. The relative potencies of these excitants on facial motoneurones are reported. The potential usefulness of N-methyl-D-aspartate to produce amino acid-evoked motoneurone action potentials is discussed. The microelectrophoretically-applied depressant amino acid antagonist strychnine selectively and reversibly blocked the depressant effects of glycine on facial motoneurones. The depression of amino acid-induced firing of facial motoneurones by stimuli to the lingual or glossopharyngeal nerves were reversibly antagonized by microelectrophoretically applied strychnine but not by bicuculline.
- Published
- 1977
- Full Text
- View/download PDF
142. The seventh cranial nerve of the rat. Visualization of efferent and afferent pathways by cobalt precipitation.
- Author
-
Martin MR and Mason CA
- Subjects
- Animals, Cobalt, Facial Muscles innervation, Lacrimal Apparatus innervation, Male, Medulla Oblongata ultrastructure, Motor Cortex ultrastructure, Motor Neurons, Gamma ultrastructure, Neural Pathways, Rats, Salivary Glands innervation, Staining and Labeling, Trigeminal Ganglion ultrastructure, Facial Nerve ultrastructure, Motor Neurons ultrastructure
- Abstract
The cobalt sulphide precipitation technique, in conjunction with Timm's intensification procedure, was used to delineate the afferent and efferent intramedullary pathways of the seventh cranial nerve complex in the rat. The branchial motor nucleus with the accompanying first part, genu, and second part of the root are described. The motor branches to the superficial facial musculature do not contain fibres of geniculate ganglion origin or fibres which terminate in the spinal trigeminal nucleus. The motor branches to the deep facial muscles arise from the dorsal part of the branchial motor nucleus and traverse to the midline medial to the genu, then project under the genu into the lateral reticular formation before exiting with the facial nerve. The salivatory and lacrimal nuclei and their intramedullary pathways are described. Sensory fibres from the cutaneous auricular branch enter the spinal trigeminal tract and most of the chorda tympani gustatory fibres enter the fasciculus solitarius. A smaller number of gustatory fibres extend medially to the region of the salivatory nucleus. Fibres of greater superficial petrosal origin also enter the fasciculus solitarius as well as the medial reticular formation. These findings are discussed in relation to previous anatomical, physiological and clinical reports.
- Published
- 1977
- Full Text
- View/download PDF
143. Lateral inhibition in the anteroventral cochlear nucleus of the cat: a microiontophoretic study.
- Author
-
Martin MR and Dickson JW
- Subjects
- Amino Acids pharmacology, Animals, Cats, Cochlea physiology, Evoked Potentials, Auditory, Female, Homocysteine analogs & derivatives, Homocysteine pharmacology, Iontophoresis, Male, Cochlea innervation, Neural Inhibition drug effects
- Abstract
The spontaneous firing rates of non-prepotential (NPP) units of the anteroventral cochlear nucleus are quite low so it has not been possible to determine whether side band tones are inhibitory when presented alone. Microiontophoretically-applied excitatory amino acids can be used to excite non-spontaneous cells directly. Using this technique it can be shown that side band tone bursts 1/2 to 3/4 octave above the characteristic frequency (CF) of a NPP unit inhibit the amino acid-induced firing. Side band tones which inhibited the amino acid-induced firing were beyond the tuning curve. Side band tones within the tuning curve produced excitation. Both, however, usually reduced the activity evoked by a CF tone burst (i.e., two-tone interaction). The data suggests that lateral inhibition and two-tone interactions are separate phenomena in the auditory system and that lateral inhibition may play a critical role in determining the shape of the tuning curve of NPP units.
- Published
- 1983
- Full Text
- View/download PDF
144. A breach of professional etiquette.
- Author
-
Martin MR
- Subjects
- Registries, United Kingdom, Confidentiality, Insurance
- Published
- 1980
- Full Text
- View/download PDF
145. Bicuculline, strychnine and depressant amino acid responses in the anteroventral cochlear nucleus of the cat.
- Author
-
Martin MR, Dickson JW, and Fex J
- Subjects
- Animals, Cats, Cochlea physiology, Depression, Chemical, Glycine pharmacology, Muscimol pharmacology, Taurine pharmacology, beta-Alanine pharmacology, gamma-Aminobutyric Acid pharmacology, Amino Acids pharmacology, Bicuculline pharmacology, Cochlea drug effects, Strychnine pharmacology
- Abstract
Experiments were conducted in the cat anteroventral cochlear nucleus, comparing the actions of strychnine and bicuculline on amino acid-induced depression of spontaneous and evoked firing. Strychnine reduced responses induced by glycine, taurine and beta-alanine more than GABA or muscimol-induced responses. These latter responses were sensitive to bicuculline. Responses to single and paired tone bursts were not sensitive to strychnine or bicuculline applied either iontophoretically or intravenously. The results indicate that the receptors for depressant amino acids are similar to the receptors found in the cat in other brainstem and spinal cord sites, but differ from those found in the cerebellum, thalamus and cerebral cortex. The data also indicate that these amino acids are not involved either in the response to tone bursts at characteristic frequency or in the suppression of this response by a second, higher frequency tone.
- Published
- 1982
- Full Text
- View/download PDF
146. Quisqualamine, a novel gamma-aminobutyric acid (GABA) related depressant amino acid.
- Author
-
Evans RH, Francis AA, Hunt K, Martin MR, and Watkins JC
- Subjects
- Amines pharmacology, Animals, Anura, Depression, Chemical, Evoked Potentials drug effects, In Vitro Techniques, Mice, Quisqualic Acid analogs & derivatives, Rats, Synaptic Transmission drug effects, gamma-Aminobutyric Acid pharmacology, Oxadiazoles pharmacology, Spinal Cord drug effects
- Abstract
A new substnace, quisqualamine, the decarboxylated analogue of quisqualic acid, predictably depressed electrical activity of neurons of the frog and rat spinal cord in vitro and of the mouse spinal cord in vivo. In the in vitro preparations, the action of quisqualamine was associated with a prolonged depolarization of primary afferent terminals which was sensitive to blockade by picrotoxin and bicuculline and which was also depressed by strychnine. This suggests an interaction of quisqualamine with presynaptic receptors for both GABA and beta-alanine. Post-synaptic actions of quisqualamine, which were less marked than those at presynaptic sites, also appeared to be predominantly GABA-mimetic in vitro, though a sensitivity to the GABA-antagonist bicuculline could not be demonstrated in vitro.
- Published
- 1978
- Full Text
- View/download PDF
147. Excitatory amino acid pharmacology of the auditory nerve and nucleus magnocellularis of the chicken.
- Author
-
Martin MR
- Subjects
- Animals, Aspartic Acid analogs & derivatives, Aspartic Acid pharmacology, Auditory Pathways drug effects, Baclofen pharmacology, Brain Stem embryology, Chick Embryo, Kainic Acid pharmacology, N-Methylaspartate, Oxadiazoles pharmacology, Quisqualic Acid, Receptors, Neurotransmitter analysis, Vestibulocochlear Nerve embryology, Amino Acids pharmacology, Brain Stem drug effects, Vestibulocochlear Nerve drug effects
- Abstract
Experiments were performed on the nucleus magnocellularis and auditory nerve in tissue slices of 19-20-day-old chick embryos. Bath-applied kainate, quisqualate and N-methyl-D-aspartate induced dose-dependent alterations in the antidromic responses of nucleus magnocellularis neurons. The sensitivity of these agonist-induced responses to 2,3-cis-piperidine dicarboxylate, glutamate diethylester and D-alpha-aminoadipate were tested, as was the sensitivity of auditory nerve transmission. The data suggest that receptors for all three agonists are present on nucleus magnocellularis neurons and that the postsynaptic receptor of the nucleus magnocellularis-auditory nerve synapse is of the kainate type. The effects of bath-applied baclofen were also studied. Baclofen blocked orthodromic responses suggesting that an excitatory amino acid is released from the presynaptic terminal.
- Published
- 1985
- Full Text
- View/download PDF
148. Generation of surgical pathology report using a 5,000-word speech recognizer.
- Author
-
Tischler AS and Martin MR
- Subjects
- Equipment and Supplies, Vocabulary, Word Processing, Artificial Intelligence, Natural Language Processing, Pathology, Surgical, Phonetics
- Abstract
Pressures to decrease both turnaround time and operating costs simultaneously have placed conflicting demands on traditional forms of medical transcription. The new technology of voice recognition extends the promise of enabling the pathologist or other medical professional to dictate a correct report and have it printed and/or transmitted to a database immediately. The usefulness of voice recognition systems depends on several factors, including ease of use, reliability, speed, and accuracy. These in turn depend on the general underlying design of the systems and inclusion in the systems of a specific knowledge base appropriate for each application. Development of a good knowledge base requires close collaboration between a domain expert and a knowledge engineer with expertise in voice recognition. The authors have recently completed a knowledge base for surgical pathology using the Kurzweil VoiceReport 5,000-word system.
- Published
- 1989
149. D-alpha-Aminoadipate as a selective antagonist of amino acid-induced and synaptic excitation of mammalian spinal neurones.
- Author
-
Biscoe TJ, Evans RH, Francis AA, Martin MR, Watkins JC, Davies J, and Dray A
- Subjects
- Animals, Aspartic Acid analogs & derivatives, Cats, Interneurons drug effects, Mice, Neurotransmitter Agents antagonists & inhibitors, Synapses physiology, 2-Aminoadipic Acid pharmacology, Action Potentials drug effects, Amino Acids, Dicarboxylic pharmacology, Aspartic Acid antagonists & inhibitors, Ganglia, Spinal drug effects, Spinal Cord drug effects
- Published
- 1977
- Full Text
- View/download PDF
150. A microelectrophoretic and electrophysiological study on normal and Jimpy mutant mouse spinal neurones and reflexes.
- Author
-
Martin MR, McHanwell S, and Biscoe TJ
- Subjects
- Amino Acids pharmacology, Animals, Evoked Potentials drug effects, Female, Iontophoresis methods, Male, Mice, Mice, Inbred C3H, Mice, Inbred Strains, Neurons drug effects, Neurons physiology, Reaction Time drug effects, Reflex drug effects, Spinal Cord drug effects, Synaptic Transmission drug effects, Reflex physiology, Spinal Cord physiology
- Published
- 1978
- Full Text
- View/download PDF
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