Canlyniadau Chwilio - Köhler, Birgit
- Dangos 1 - 18 canlyniadau o 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... gan Köhler, Birgit, Lin, Lin, Mazen, Inas, Cetindag, Cigdem, Biebermann, Heike, Akkurt, Ilker, Rossi, Rainer, Hiort, Olaf, Grüters, Annette, Achermann, John C
Cyhoeddwyd 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... gan Rapp, Marion, Mueller-Godeffroy, Esther, Lee, Peter, Roehle, Robert, Kreukels, Baudewijntje P. C., Köhler, Birgit, Nordenström, Anna, Bouvattier, Claire, Thyen, Ute
Cyhoeddwyd 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 gan Tantawy, Sally, Lin, Lin, Akkurt, Ilker, Borck, Guntram, Klingmüller, Dietrich, Hauffa, Berthold P, Krude, Heiko, Biebermann, Heike, Achermann, John C, Köhler, Birgit
Cyhoeddwyd 2012Text -
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Caring for individuals with a difference of sex development (DSD): a Consensus Statement gan Cools, Martine, Nordenström, Anna, Robeva, Ralitsa, Hall, Joanne, Westerveld, Puck, Flück, Christa, Köhler, Birgit, Berra, Marta, Springer, Alexander, Schweizer, Katinka, Pasterski, Vickie
Cyhoeddwyd 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 gan Köhler, Birgit, Lin, Lin, Ferraz-de-Souza, Bruno, Wieacker, Peter, Heidemann, Peter, Schröder, Vanessa, Biebermann, Heike, Schnabel, Dirk, Grüters, Annette, Achermann, John C
Cyhoeddwyd 2008Text -
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Health status in 1040 adults with disorders of sex development (DSD): a European multicenter study gan Falhammar, Henrik, Claahsen-van der Grinten, Hedi, Reisch, Nicole, Slowikowska-Hilczer, Jolanta, Nordenström, Anna, Roehle, Robert, Bouvattier, Claire, Kreukels, Baudewijntje P C, Köhler, Birgit
Cyhoeddwyd 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 gan 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
Cyhoeddwyd 2017Text -
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Biodiversity of mycobial communities in health and onychomycosis gan 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.
Cyhoeddwyd 2022Text -
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Sleep Timing in Patients with Precocious and Delayed Pubertal Development gan 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
Cyhoeddwyd 2019Text -
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Mental Health of a Large Group of Adults With Disorders of Sex Development in Six European Countries gan 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.
Cyhoeddwyd 2019Text -
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Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency gan 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
Cyhoeddwyd 2011Text -
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Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency gan 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.
Cyhoeddwyd 2021Text -
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Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency gan 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
Cyhoeddwyd 2012Text