Quality of Life in Late-Treated Patients With Disorders of Sex Development: Insights for Patient-Centered Care

por Ediati, Annastasia, Verrips, Gijsbert H. W., Juniarto, Achmad Zulfa, Faradz, Sultana M. H., Drop, Stenvert L. S., Dessens, Arianne B.
Publicado 2019

Do Surgical Interventions Influence Psychosexual and Cosmetic Outcomes in Women with Disorders of Sex Development?

por Callens, Nina, van der Zwan, Yvonne G., Drop, Stenvert L. S., Cools, Martine, Beerendonk, Catharina M., Wolffenbuttel, Katja P., Dessens, Arianne B.
Publicado 2012

Delayed Recognition of Disorders of Sex Development (DSD): A Missed Opportunity for Early Diagnosis of Malignant Germ Cell Tumors

por Hersmus, Remko, Stoop, Hans, White, Stefan J., Drop, Stenvert L. S., Oosterhuis, J. Wolter, Incrocci, Luca, Wolffenbuttel, Katja P., Looijenga, Leendert H. J.
Publicado 2012

Multilingual Global E-Learning Pediatric Endocrinology and Diabetes Curriculum for Front Line Health Care Providers in Resource-Limited Countries: Development Study

por Kalaitzoglou, Evangelia, Majaliwa, Edna, Zacharin, Margaret, de Beaufort, Carine, Chanoine, Jean-Pierre, van Wijngaard-DeVugt, Conny, Sperla, Ervin, Boot, Annemieke M, Drop, Stenvert L S
Publicado 2020

Sexual Self-Concept in Women with Disorders/Differences of Sex Development

por de Neve-Enthoven, Nita G. M., Callens, Nina, van Kuyk, Maaike, Verhaak, Chris M., van der Ende, Jan, Drop, Stenvert L. S., Cohen-Kettenis, Peggy T., Dessens, Arianne B.
Publicado 2022

Corrigendum: Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country

por Utari, Agustini, Faradz, Sultana M. H., Ediati, Annastasia, Rinne, Tuula, Ariani, Mahayu Dewi, Juniarto, Achmad Zulfa, Drop, Stenvert L. S., van Herwaarden, Antonius E., Claahsen-van der Grinten, Hedi L.
Publicado 2023

Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country

por Utari, Agustini, Faradz, Sultana M. H., Ediati, Annastasia, Rinne, Tuula, Ariani, Mahayu Dewi, Juniarto, Achmad Zulfa, Drop, Stenvert L. S., van Herwaarden, Antonius E., Claahsen-van der Grinten, Hedi L.
Publicado 2022

Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans

por Zhong, Kaiyin, Zhu, Gu, Jing, Xiaoxi, Hendriks, A. Emile J., Drop, Sten L. S., Ikram, M. Arfan, Gordon, Scott, Zeng, Changqing, Uitterlinden, Andre G., Martin, Nicholas G., Liu, Fan, Kayser, Manfred
Publicado 2017

Androgen Receptor Function Links Human Sexual Dimorphism to DNA Methylation

por Ammerpohl, Ole, Bens, Susanne, Appari, Mahesh, Werner, Ralf, Korn, Bernhard, Drop, Stenvert L. S., Verheijen, Frans, van der Zwan, Yvonne, Bunch, Trevor, Hughes, Ieuan, Cools, Martine, Riepe, Felix G., Hiort, Olaf, Siebert, Reiner, Holterhus, Paul-Martin
Publicado 2013

Prevalence of c-KIT Mutations in Gonadoblastoma and Dysgerminomas of Patients with Disorders of Sex Development (DSD) and Ovarian Dysgerminomas

por Hersmus, Remko, Stoop, Hans, van de Geijn, Gert Jan, Eini, Ronak, Biermann, Katharina, Oosterhuis, J. Wolter, DHooge, Catharina, Schneider, Dominik T., Meijssen, Isabelle C., Dinjens, Winand N. M., Dubbink, Hendrikus Jan, Drop, Stenvert L. S., Looijenga, Leendert H. J.
Publicado 2012

Application of the New Classification on Patients with a Disorder of Sex Development in Indonesia

por Juniarto, A. Zulfa, van der Zwan, Yvonne G., Santosa, Ardy, Hersmus, Remko, de Jong, Frank H., Olmer, Renske, Bruggenwirth, Hennie T., Themmen, Axel P. N., Wolffenbuttel, Katja P., Looijenga, Leendert H. J., Faradz, Sultana M. H., Drop, Stenvert L. S.
Publicado 2012

A 46,XY Female DSD Patient with Bilateral Gonadoblastoma, a Novel SRY Missense Mutation Combined with a WT1 KTS Splice-Site Mutation

por Hersmus, Remko, van der Zwan, Yvonne G., Stoop, Hans, Bernard, Pascal, Sreenivasan, Rajini, Oosterhuis, J. Wolter, Brüggenwirth, Hennie T., de Boer, Suzan, White, Stefan, Wolffenbuttel, Katja P., Alders, Marielle, McElreavy, Kenneth, Drop, Stenvert L. S., Harley, Vincent R., Looijenga, Leendert H. J.
Publicado 2012

Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity

por Hornig, N. C., Ukat, M., Schweikert, H. U., Hiort, O., Werner, R., Drop, S. L. S., Cools, M., Hughes, I. A., Audi, L., Ahmed, S. F., Demiri, J., Rodens, P., Worch, L., Wehner, G., Kulle, A. E., Dunstheimer, D., Müller-Roßberg, E., Reinehr, T., Hadidi, A. T., Eckstein, A. K., van der Horst, C., Seif, C., Siebert, R., Ammerpohl, O., Holterhus, P.-M.
Publicado 2016