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11 results on '"Glosli, Heidi"'

1. Outcomes in lung-only metastatic rhabdomyosarcoma: An analysis of data from the European paediatric Soft tissue sarcoma Study Group MTS 2008 study

Author

Chisholm, Julia C., Schoot, Reineke A., Cameron, Alison L., Casanova, Michela, Minard-Colin, Veronique, Coppadoro, Beatrice, Garrido, Marta, Rogers, Timothy, Orbach, Daniel, Glosli, Heidi, Ben-Arush, Miriam, Ferman, Sima, Scarzello, Giovanni, van Rijn, Rick R., Hladun, Raquel, Corradini, Nadege, Ferrari, Andrea, Jenney, Meriel, Bisogno, Gianni, and Merks, Johannes H.M.

Published
2023
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4. Effect of Music Therapy on Parent-Infant Bonding Among Infants Born Preterm

Author

Ghetti, Claire M., primary, Gaden, Tora Söderström, additional, Bieleninik, Łucja, additional, Kvestad, Ingrid, additional, Assmus, Jörg, additional, Stordal, Andreas Størksen, additional, Aristizabal Sanchez, Luisa Fernanda, additional, Arnon, Shmuel, additional, Dulsrud, Jeanette, additional, Elefant, Cochavit, additional, Epstein, Shulamit, additional, Ettenberger, Mark, additional, Glosli, Heidi, additional, Konieczna-Nowak, Ludwika, additional, Lichtensztejn, Marcela, additional, Lindvall, Merethe Wolf, additional, Mangersnes, Julie, additional, Murcia Fernández, Luz Dary, additional, Røed, Catharina Janner, additional, Saá, Gladys, additional, Van Roy, Betty, additional, Vederhus, Bente Johanne, additional, and Gold, Christian, additional

Published
2023
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6. Brachytherapy for pediatric patients at Gustave Roussy Cancer Campus: A model of international cooperation for highly specialized treatments

Author

Chargari, Cyrus Haie-Meder, Christine Espenel, Sophie Garcia, Max-Adrien Ben-Arush, Myriam Bolle, Stéphanie Borjesson, Anna Cesen, Maja Lago, Rita Costa Defachelles, Anne-Sophie De Moerloose, Barbara Devalck, Christine Edslev, Pernille Farinha, Nuno Jorge Francotte, Nadine Glosli, Heidi Gouy, Sebastien Burrieza, Gabriela Guillen Helfre, Sylvie Irtan, Sabine Kattamis, Antonis Lacerda, Ana Levy, Antonin Hjalgrim, Lisa Lyngsie Mansuy, Ludovic Mascard, Eric Moalla, Salma Orbach, Daniel Owens, Cormac Philippe-Chomette, Pascale Pizer, Barry Pluchart, Claire Renard, Marleen Rognlien, Anne Gro Wesenberg Rome, Angélique Sarnacki, Sabine Safwat, Akmal Schiavetti, Amalia Serre, Jill Verite, Cécile Weid, Nicolas Von Der Wysocki, Mariusz Valteay-Couanet, Dominique Deutsch, Eric Minard-Colin, Véronique Martelli, Hélène Guérin, Florent

Abstract

PURPOSE: Childhood cancer is rare, and treatment is frequently associated with long-term morbidity. Disparities in survival and long-term side-effects encourage the establishment of networks to increase access to complex organ conservative strategies, such as brachytherapy (BT). We report our experience of an international cooperation model in childhood cancers. METHODS AND MATERIALS: We examined the outcome of all children referred to our center from national or international networks to be treated according to a multimodal organ-conservative approach including BT. RESULTS: 305 patients were identified; median age at diagnosis was 2.2 years (1.4 months-17.2 years). Ninety-nine (32.4%) were treated within 2015-2020. One hundred seventy-two (56.4%) were referred from national centers and 133 (43.6%) were international patients, from 31 countries (mainly Europe). Two hundred sixty three patients were referred for primary treatment and 42 for salvage treatment. Genito-urinary tumors were the most frequent sites, with 56.4% bladder/prostate rhabdomyosarcoma (RMS) and 28.5% gynecological tumors. In addition to BT, local treatment comprised partial tumor resection in 207 (67.9%) and 39 (13%) had additional external radiotherapy. Median follow-up was 58 months (range: 1 month-48 years), 93 months for national patients and 37 months for international patients (p

Published
2022

7. Molecular Characterization of Two Homozygous Factor VII Variants Associated with Intracranial Bleeding

Author

Andersen, Elisabeth, primary, Chollet, Maria Eugenia, additional, Sletten, Marit, additional, Stavik, Benedicte, additional, Myklebust, Christiane Filion, additional, Skarpen, Ellen, additional, Hoff Backe, Paul, additional, Sandset, Per Morten, additional, Glosli, Heidi, additional, Henriksson, Carola, additional, and Iversen, Nina, additional

Published
2020
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8. Local staging and treatment in extremity rhabdomyosarcoma. A report from the EpSSG‐RMS2005 study

Author

Terwisscha van Scheltinga, Sheila E. J., primary, Wijnen, Marc H. W. A., additional, Martelli, Hélène, additional, Rogers, Timothy, additional, Mandeville, Henry, additional, Gaze, Mark N., additional, McHugh, Keiran, additional, Corradini, Nadege, additional, Orbach, Daniel, additional, Jenney, Meriel, additional, Kelsey, Anna, additional, Chisholm, Julia, additional, Gallego, Soledad, additional, Glosli, Heidi, additional, Ferrari, Andrea, additional, Zanetti, Ilaria, additional, De Salvo, Gian Luca, additional, Minard‐Colin, Veronique, additional, Bisogno, Giani, additional, van Noesel, Max M., additional, and Merks, Hans H. M., additional

Published
2020
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11. Infections due to various atypical mycobacteria in a Norwegian multiplex family with dominant interferon-gamma receptor deficiency.

Author

Glosli H, Stray-Pedersen A, Brun AC, Holtmon LW, Tønjum T, Chapgier A, Casanova JL, and Abrahamsen TG

Subjects
Adolescent, Child, Female, Genes, Dominant, Genetic Predisposition to Disease, Humans, Male, Mycobacterium Infections, Nontuberculous drug therapy, Mycobacterium Infections, Nontuberculous immunology, Mycobacterium Infections, Nontuberculous microbiology, Norway, Pedigree, Polymerase Chain Reaction methods, RNA, Ribosomal, 16S genetics, Receptors, Interferon genetics, Receptors, Interferon immunology, Interferon gamma Receptor, Mycobacterium Infections, Nontuberculous genetics, Nontuberculous Mycobacteria isolation & purification, Receptors, Interferon deficiency
Abstract

Background: Atypical mycobacteria can cause systemic infections in patients with certain types of immunodeficiency., Methods: Clinical samples were decontaminated and cultured to assess the presence of mycobacterial species. Gene sequencing was performed to reveal interferon-gamma receptor 1 (IFN-gamma R1) deficiency., Results: The index patient received a diagnosis of dominant IFN-gamma R1 deficiency during treatment for a serious infection due to atypical mycobacteria. She belongs to a Norwegian multiplex family comprising 3 generations and 5 patients with dominant IFN-gamma R1 deficiency. Four of these patients have been treated with tuberculostatics because of extensive infection due to atypical mycobacteria, such as Mycobacterium avium-intracellulare, Mycobacterium scrofulaceum, Mycobacterium bovis (bacille Calmette-Guérin), Mycobacterium bohemicum, and Mycobacterium gordonae. Two of the patients have also received subcutaneous injections of IFN-gamma. One family member with the deficiency has not received treatment and is still healthy at 13 years of age., Conclusions: Serious infection due to atypical mycobacteria should initiate a search for primary immunodeficiencies, particularly IFN-gamma R1 deficiency. Treatment with IFN-gamma should be started when serious infection due to atypical mycobacteria is verified and dominant partial IFN-gamma R1 deficiency is suspected.

Published
2008
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