Resultats de la cerca - Köhler, Birgit
- Mostrar 1 - 18 resultats de 18
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The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insuffici... per Köhler, Birgit, Lin, Lin, Mazen, Inas, Cetindag, Cigdem, Biebermann, Heike, Akkurt, Ilker, Rossi, Rainer, Hiort, Olaf, Grüters, Annette, Achermann, John C
Publicat 2009Text -
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Multicentre cross-sectional clinical evaluation study about quality of life in adults with disorders/differences of sex development (DSD) compared to country specific reference pop... per Rapp, Marion, Mueller-Godeffroy, Esther, Lee, Peter, Roehle, Robert, Kreukels, Baudewijntje P. C., Köhler, Birgit, Nordenström, Anna, Bouvattier, Claire, Thyen, Ute
Publicat 2018Text -
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Testosterone production during puberty in two 46,XY patients with disorders of sex development and novel NR5A1 (SF-1) mutations per Tantawy, Sally, Lin, Lin, Akkurt, Ilker, Borck, Guntram, Klingmüller, Dietrich, Hauffa, Berthold P, Krude, Heiko, Biebermann, Heike, Achermann, John C, Köhler, Birgit
Publicat 2012Text -
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Caring for individuals with a difference of sex development (DSD): a Consensus Statement per Cools, Martine, Nordenström, Anna, Robeva, Ralitsa, Hall, Joanne, Westerveld, Puck, Flück, Christa, Köhler, Birgit, Berra, Marta, Springer, Alexander, Schweizer, Katinka, Pasterski, Vickie
Publicat 2018Text -
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Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency per Köhler, Birgit, Lin, Lin, Ferraz-de-Souza, Bruno, Wieacker, Peter, Heidemann, Peter, Schröder, Vanessa, Biebermann, Heike, Schnabel, Dirk, Grüters, Annette, Achermann, John C
Publicat 2008Text -
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Health status in 1040 adults with disorders of sex development (DSD): a European multicenter study per Falhammar, Henrik, Claahsen-van der Grinten, Hedi, Reisch, Nicole, Slowikowska-Hilczer, Jolanta, Nordenström, Anna, Roehle, Robert, Bouvattier, Claire, Kreukels, Baudewijntje P C, Köhler, Birgit
Publicat 2018Text -
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Participation of adults with disorders/differences of sex development (DSD) in the clinical study dsd-LIFE: design, methodology, recruitment, data quality and study population per Röhle, Robert, Gehrmann, Katharina, Szarras-Czapnik, Maria, Claahsen-van der Grinten, Hedi, Pienkowski, Catherine, Bouvattier, Claire, Cohen-Kettenis, Peggy, Nordenström, Anna, Thyen, Ute, Köhler, Birgit
Publicat 2017Text -
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Biodiversity of mycobial communities in health and onychomycosis per Olbrich, Michael, Ernst, Anna Lara, Beltsiou, Foteini, Bieber, Katja, Ständer, Sascha, Harder, Melanie, Anemüller, Waltraud, Köhler, Birgit, Zillikens, Detlef, Busch, Hauke, Künstner, Axel, Ludwig, Ralf J.
Publicat 2022Text -
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Sleep Timing in Patients with Precocious and Delayed Pubertal Development per Jessen, Elena, Vetter, Celine, Roenneberg, Till, Liesenkötter, Klaus-Peter, Werner, Helene, Jenni, Oskar G., Lankes, Erwin, Blankenstein, Oliver, Neumann, Uta, Köhler, Birgit, Wiegand, Susanna, Krude, Heiko, Kühnen, Peter
Publicat 2019Text -
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Mental Health of a Large Group of Adults With Disorders of Sex Development in Six European Countries per de Vries, Annelou L.C., Roehle, Robert, Marshall, Louise, Frisén, Louise, van de Grift, Tim C., Kreukels, Baudewijntje P.C., Bouvattier, Claire, Köhler, Birgit, Thyen, Ute, Nordenström, Anna, Rapp, Marion, Cohen-Kettenis, Peggy T.
Publicat 2019Text -
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Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency per Idkowiak, Jan, O'Riordan, Stephen, Reisch, Nicole, Malunowicz, Ewa M., Collins, Felicity, Kerstens, Michiel N., Köhler, Birgit, Graul-Neumann, Luitgard Margarete, Szarras-Czapnik, Maria, Dattani, Mehul, Silink, Martin, Shackleton, Cedric H. L., Maiter, Dominique, Krone, Nils, Arlt, Wiebke
Publicat 2011Text -
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Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency per Verhees, Myrthe J. M., Engels, Manon, Span, Paul N., Sweep, Fred C. G. J., van Herwaarden, Antonius E., Falhammar, Henrik, Nordenström, Anna, Webb, Emma A., Richter-Unruh, Annette, Bouvattier, Claire, de la Perrière, Aude Brac, Arlt, Wiebke, Reisch, Nicole, Köhler, Birgit, Rapp, Marion, Stikkelbroeck, Nike M. M. L., Roeleveld, Nel, Claahsen-van der Grinten, Hedi L.
Publicat 2021Text -
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Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency per Krone, Nils, Reisch, Nicole, Idkowiak, Jan, Dhir, Vivek, Ivison, Hannah E., Hughes, Beverly A., Rose, Ian T., O'Neil, Donna M., Vijzelaar, Raymon, Smith, Matthew J., MacDonald, Fiona, Cole, Trevor R., Adolphs, Nicolai, Barton, John S., Blair, Edward M., Braddock, Stephen R., Collins, Felicity, Cragun, Deborah L., Dattani, Mehul T., Day, Ruth, Dougan, Shelley, Feist, Miriam, Gottschalk, Michael E., Gregory, John W., Haim, Michaela, Harrison, Rachel, Haskins Olney, Ann, Hauffa, Berthold P., Hindmarsh, Peter C., Hopkin, Robert J., Jira, Petr E., Kempers, Marlies, Kerstens, Michiel N., Khalifa, Mohamed M., Köhler, Birgit, Maiter, Dominique, Nielsen, Shelly, O'Riordan, Stephen M., Roth, Christian L., Shane, Kate P., Silink, Martin, Stikkelbroeck, Nike M. M. L., Sweeney, Elizabeth, Szarras-Czapnik, Maria, Waterson, John R., Williamson, Lori, Hartmann, Michaela F., Taylor, Norman F., Wudy, Stefan A., Malunowicz, Ewa M., Shackleton, Cedric H. L., Arlt, Wiebke
Publicat 2012Text