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20 results on '"Hove, Hanne D."'

2. Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting

Author

Saadi, Irfan, Alkuraya, Fowzan S., Gisselbrecht, Stephen S., Goessling, Wolfram, Cavallesco, Resy, Turbe-Doan, Annick, Petrin, Aline L., Harris, James, Siddiqui, Ursela, Grix, Arthur W., Jr., Hove, Hanne D., Leboulch, Philippe, Glover, Thomas W., Morton, Cynthia C., Richieri-Costa, Antonio, Murray, Jeffrey C., Erickson, Robert P., and Maas, Richard L.

Published
2011
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3. A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype

Author

Terhal, Paulien A., Nievelstein, Rutger Jan A. J., Verver, Eva J. J., Topsakal, Vedat, van Dommelen, Paula, Hoornaert, Kristien, Le Merrer, Martine, Zankl, Andreas, Simon, Marleen E. H., Smithson, Sarah F., Marcelis, Carlo, Kerr, Bronwyn, Clayton-Smith, Jill, Kinning, Esther, Mansour, Sahar, Elmslie, Frances, Goodwin, Linda, van der Hout, Annemarie H., Veenstra-Knol, Hermine E., Herkert, Johanna C., Lund, Allan M., Hennekam, Raoul C. M., Mégarbané, André, Lees, Melissa M., Wilson, Louise C., Male, Alison, Hurst, Jane, Alanay, Yasemin, Annerén, Göran, Betz, Regina C., Bongers, Ernie M. H. F., Cormier-Daire, Valerie, Dieux, Anne, David, Albert, Elting, Mariet W., van den Ende, Jenneke, Green, Andrew, van Hagen, Johanna M., Hertel, Niels Thomas, Holder-Espinasse, Muriel, den Hollander, Nicolette, Homfray, Tessa, Hove, Hanne D., Price, Susan, Raas-Rothschild, Annick, Rohrbach, Marianne, Schroeter, Barbara, Suri, Mohnish, Thompson, Elizabeth M., Tobias, Edward S., Toutain, Annick, Vreeburg, Maaike, Wakeling, Emma, Knoers, Nine V., Coucke, Paul, and Mortier, Geert R.

Published
2015
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6. Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder

Author

Rutten, Bart P. F., Vermetten, E, Vinkers, C H, Ursini, G, Daskalakis, N.P., Pishva, E., de Nijs, Laurence, Houtepen, L C, Eijssen, L.M., Jaffe, A E, Kenis, G., Viechtbauer, W., Hove, Hanne D., Schraut, K G, Lesch, K.P., Kleinman, J E, Hyde, T M, Weinberger, Daniel R., Schalkwyk, L.C., Lunnon, Katie, Mill, J., Cohen, M.H., Yehuda, R., Baker, Dewleen G., Maihofer, Adam X., Nievergelt, Caroline M., Geuze, E, Boks, M P M, Rutten, Bart P. F., Vermetten, E, Vinkers, C H, Ursini, G, Daskalakis, N.P., Pishva, E., de Nijs, Laurence, Houtepen, L C, Eijssen, L.M., Jaffe, A E, Kenis, G., Viechtbauer, W., Hove, Hanne D., Schraut, K G, Lesch, K.P., Kleinman, J E, Hyde, T M, Weinberger, Daniel R., Schalkwyk, L.C., Lunnon, Katie, Mill, J., Cohen, M.H., Yehuda, R., Baker, Dewleen G., Maihofer, Adam X., Nievergelt, Caroline M., Geuze, E, and Boks, M P M

Published
2018

7. Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder

Author

MGGZ, Brain, Diagnostiek & Vroege Psychose Medisch, Onderzoeksgroep 2, Rutten, Bart P. F., Vermetten, E, Vinkers, C H, Ursini, G, Daskalakis, N.P., Pishva, E., de Nijs, Laurence, Houtepen, L C, Eijssen, L.M., Jaffe, A E, Kenis, G., Viechtbauer, W., Hove, Hanne D., Schraut, K G, Lesch, K.P., Kleinman, J E, Hyde, T M, Weinberger, Daniel R., Schalkwyk, L.C., Lunnon, Katie, Mill, J., Cohen, M.H., Yehuda, R., Baker, Dewleen G., Maihofer, Adam X., Nievergelt, Caroline M., Geuze, E, Boks, M P M, MGGZ, Brain, Diagnostiek & Vroege Psychose Medisch, Onderzoeksgroep 2, Rutten, Bart P. F., Vermetten, E, Vinkers, C H, Ursini, G, Daskalakis, N.P., Pishva, E., de Nijs, Laurence, Houtepen, L C, Eijssen, L.M., Jaffe, A E, Kenis, G., Viechtbauer, W., Hove, Hanne D., Schraut, K G, Lesch, K.P., Kleinman, J E, Hyde, T M, Weinberger, Daniel R., Schalkwyk, L.C., Lunnon, Katie, Mill, J., Cohen, M.H., Yehuda, R., Baker, Dewleen G., Maihofer, Adam X., Nievergelt, Caroline M., Geuze, E, and Boks, M P M

Published
2018

8. Circulating microRNAs as potential biomarkers of differential susceptibility to traumatic stress

Author

de Nijs, Laurence, Krauskopf, Julian, Snijders, C., Kleinjans, J. C S, Machiels, Barbie, Smeets, B., Kenis, G., Hove, Hanne D., Vinkers, C., Geuze, E., Boks, M., Vermetten, E., Rutten, B., de Nijs, Laurence, Krauskopf, Julian, Snijders, C., Kleinjans, J. C S, Machiels, Barbie, Smeets, B., Kenis, G., Hove, Hanne D., Vinkers, C., Geuze, E., Boks, M., Vermetten, E., and Rutten, B.

Published
2017

9. Circulating microRNAs as potential biomarkers of differential susceptibility to traumatic stress

Author

Huisartsopleiding Intern, Diagnostiek & Vroege Psychose Medisch, Brain, MGGZ, Onderzoeksgroep 2, de Nijs, Laurence, Krauskopf, Julian, Snijders, C., Kleinjans, J. C S, Machiels, Barbie, Smeets, B., Kenis, G., Hove, Hanne D., Vinkers, C., Geuze, E., Boks, M., Vermetten, E., Rutten, B., Huisartsopleiding Intern, Diagnostiek & Vroege Psychose Medisch, Brain, MGGZ, Onderzoeksgroep 2, de Nijs, Laurence, Krauskopf, Julian, Snijders, C., Kleinjans, J. C S, Machiels, Barbie, Smeets, B., Kenis, G., Hove, Hanne D., Vinkers, C., Geuze, E., Boks, M., Vermetten, E., and Rutten, B.

Published
2017

13. A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype

Author

Genetica Klinische Genetica, Child Health, Arts-assistenten Radiologie, Other research (not in main researchprogram), MS KNO, Genetica, Terhal, Paulien A., Nievelstein, Rutger Jan, Verver, Eva J. J., Topsakal, Vedat, van Dommelen, Paula, Hoornaert, Kristien, Le Merrer, Martine, Zankl, Andreas, Simon, Marleen E. H., Smithson, Sarah F., Marcelis, Carlo, Kerr, Bronwyn, Clayton-Smith, Jill, Kinning, Esther, Mansour, Sahar, Elmslie, Frances, Goodwin, Linda, van der Hout, Annemarie H., Veenstra-Knol, Hermine E., Herkert, Johanna C., Lund, Allan M., Hennekam, Raoul C. M., Megarbane, Andre, Lees, Melissa M., Wilson, Louise C., Male, Alison, Hurst, Jane, Alanay, Yasemin, Anneren, Goeran, Betz, Regina C., Bongers, Ernie M. H. F., Cormier-Daire, Valerie, Dieux, Anne, David, Albert, Elting, Mariet W., van den Ende, Jenneke, Green, Andrew, van Hagen, Johanna M., Hertel, Niels Thomas, Holder-Espinasse, Muriel, den Hollander, Nicolette, Homfray, Tessa, Hove, Hanne D., Price, Susan, Raas-Rothschild, Annick, Rohrbach, Marianne, Schroeter, Barbara, Suri, Mohnish, Thompson, Elizabeth M., Tobias, Edward S., Toutain, Annick, Vreeburg, Maaike, Wakeling, Emma, Knoers, Nine V., Coucke, Paul, Mortier, Geert R., Genetica Klinische Genetica, Child Health, Arts-assistenten Radiologie, Other research (not in main researchprogram), MS KNO, Genetica, Terhal, Paulien A., Nievelstein, Rutger Jan, Verver, Eva J. J., Topsakal, Vedat, van Dommelen, Paula, Hoornaert, Kristien, Le Merrer, Martine, Zankl, Andreas, Simon, Marleen E. H., Smithson, Sarah F., Marcelis, Carlo, Kerr, Bronwyn, Clayton-Smith, Jill, Kinning, Esther, Mansour, Sahar, Elmslie, Frances, Goodwin, Linda, van der Hout, Annemarie H., Veenstra-Knol, Hermine E., Herkert, Johanna C., Lund, Allan M., Hennekam, Raoul C. M., Megarbane, Andre, Lees, Melissa M., Wilson, Louise C., Male, Alison, Hurst, Jane, Alanay, Yasemin, Anneren, Goeran, Betz, Regina C., Bongers, Ernie M. H. F., Cormier-Daire, Valerie, Dieux, Anne, David, Albert, Elting, Mariet W., van den Ende, Jenneke, Green, Andrew, van Hagen, Johanna M., Hertel, Niels Thomas, Holder-Espinasse, Muriel, den Hollander, Nicolette, Homfray, Tessa, Hove, Hanne D., Price, Susan, Raas-Rothschild, Annick, Rohrbach, Marianne, Schroeter, Barbara, Suri, Mohnish, Thompson, Elizabeth M., Tobias, Edward S., Toutain, Annick, Vreeburg, Maaike, Wakeling, Emma, Knoers, Nine V., Coucke, Paul, and Mortier, Geert R.

Published
2015

14. Plexiform neurofibroma of the eye region occurring in patients without neurofibromatosis type 1

Author

Bechtold, Dorte, Hove, Hanne D, Prause, Jan Ulrik, Heegaard, Steffen, Toft, Peter B, Bechtold, Dorte, Hove, Hanne D, Prause, Jan Ulrik, Heegaard, Steffen, and Toft, Peter B

Abstract

The purpose of the present study was to investigate the correlation between Plexiform Neurofibroma (PN) of the eye region and Neurofibromatosis type 1 (NF1). According to the textbooks of ophthalmology, PN and NF1 are very closely linked. Our clinical experience raised doubts about this, however.

Published
2012

15. The Cardiac Phenotype in Patients With a CHD7 Mutation

Author

Corsten-Janssen, Nicole, primary, Kerstjens-Frederikse, Wilhelmina S., additional, du Marchie Sarvaas, Gideon J., additional, Baardman, Maria E., additional, Bakker, Marian K., additional, Bergman, Jorieke E.H., additional, Hove, Hanne D., additional, Heimdal, Ketil R., additional, Rustad, Cecilie F., additional, Hennekam, Raoul C.M., additional, Hofstra, Robert M.W., additional, Hoefsloot, Lies H., additional, Van Ravenswaaij-Arts, Conny M.A., additional, and Kapusta, Livia, additional

Published
2013
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16. Craniofacial morphology in Muenke syndrome

Author

Keller, Mette Kirstine, Hermann, Nuno V, Darvann, Tron A, Larsen, Per, Hove, Hanne D, Christensen, Leif, Schwartz, Marianne, Marsh, Jeffrey L, Kreiborg, Sven, Keller, Mette Kirstine, Hermann, Nuno V, Darvann, Tron A, Larsen, Per, Hove, Hanne D, Christensen, Leif, Schwartz, Marianne, Marsh, Jeffrey L, and Kreiborg, Sven

Abstract

The purpose of this study was to test whether the severity of the cranial phenotype in Muenke syndrome infants with unicoronal synostosis is greater than in infants with nonsyndromic unicoronal synostosis. A total of 23 infants were included in the study. All infants included in the study had a computed tomography (CT)-verified synostosis of the coronal suture. The patients were either placed into the "Muenke" group (n=11) or the "non-Muenke" control group (n=12) on the basis of a test for the P250R mutation in the FGFR3 gene. On the basis of CT scans, a three-dimensional surface model corresponding to bone was created for each individual. The sutures were inspected for synostosis, and the degree of synostosis was assessed. Increased digital markings were recorded for both groups. Craniofacial morphology was assessed quantitatively using bony landmarks and recording of the midsagittal surface of the calvaria, cranial base, and maxillary complex. Increased digital markings were more severe posteriorly in Muenke patients than in non-Muenke patients. The Muenke patients with unilateral coronal synostosis showed a somewhat more severe asymmetry in the anterior part of the skull than the non-Muenke patients. The study indicates differences with regard to severity of increased digital markings and craniofacial asymmetry between the infants with Muenke syndrome and the infants with nonsyndromic unilateral coronal synostosis.

Published
2007

19. Craniofacial Morphology in Muenke Syndrome

Author

Keller, Mette K., primary, Hermann, Nuno V., additional, Darvann, Tron A., additional, Larsen, Per, additional, Hove, Hanne D., additional, Christensen, Leif, additional, Schwartz, Marianne, additional, Marsh, Jeffrey L., additional, and Kreiborg, Sven, additional

Published
2007
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20. [Life-threatening subgaleal bleeding in a newborn infant].

Author

Dahl KW, Hove HD, and Albertsen P

Subjects
Bandages, Birth Injuries therapy, Hematoma therapy, Humans, Infant, Infant, Newborn, Male, Birth Injuries etiology, Hematoma etiology, Scalp injuries, Vacuum Extraction, Obstetrical adverse effects
Abstract

Subgaleal haematoma, also called subaponeurotic haemorrhage, is a serious but rarely seen form of bleeding that can occur as a complication to vacuum-assisted delivery. Subgaleal haemorrhage may be much more copious than the more common subperiostal bleeding, and can almost exsanguinate the infant. A pressure bandage applied to the upper head can be lifesaving.

Published
2002

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