Hasil Pencarian - Stenvert L.S. Drop

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  1. 1
    An interactive E-Learning Portal in Pediatric Endocrinology: Practical Experience

    An interactive E-Learning Portal in Pediatric Endocrinology: Practical Experience oleh Stenvert L. S. Drop, Kalinka Grijpink-van den Biggelaar, Laura J. C. Kranenburg-van Koppen

    Diterbitkan 2013-10-01
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  2. 2
    Delayed Recognition of Disorders of Sex Development (DSD): A Missed Opportunity for Early Diagnosis of Malignant Germ Cell Tumors

    Delayed Recognition of Disorders of Sex Development (DSD): A Missed Opportunity for Early Diagnosis of Malignant Germ Cell Tumors oleh Remko Hersmus, Hans Stoop, Stefan J. White, Stenvert L. S. Drop, J. Wolter Oosterhuis, Luca Incrocci, Katja P. Wolffenbuttel, Leendert H. J. Looijenga

    Diterbitkan 2012-01-01
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  3. 3
    Salivary 17-hydroxyprogesterone (17-OHP) and androstenedione in monitoring efficacy of treatment among Indonesian Congenital Adrenal Hyperplasia Patients

    Salivary 17-hydroxyprogesterone (17-OHP) and androstenedione in monitoring efficacy of treatment among Indonesian Congenital Adrenal Hyperplasia Patients oleh Achmad Zulfa Juniarto, Gerard Noppe, Nani Maharani, Erica van den Akker, Rudy Susanto, Sultana MH Faradz, Frank H. de Jong, Stenvert L.S. Drop

    Diterbitkan 2014-05-01
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  4. 4
    Quality of Life in Late-Treated Patients With Disorders of Sex Development: Insights for Patient-Centered Care

    Quality of Life in Late-Treated Patients With Disorders of Sex Development: Insights for Patient-Centered Care oleh Annastasia Ediati, Annastasia Ediati, Gijsbert H. W. Verrips, Achmad Zulfa Juniarto, Achmad Zulfa Juniarto, Sultana M. H. Faradz, Sultana M. H. Faradz, Stenvert L. S. Drop, Arianne B. Dessens

    Diterbitkan 2019-01-01
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  5. 5
    Corrigendum: Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country

    Corrigendum: Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country oleh Agustini Utari, Agustini Utari, Sultana M. H. Faradz, Annastasia Ediati, Annastasia Ediati, Tuula Rinne, Mahayu Dewi Ariani, Achmad Zulfa Juniarto, Stenvert L. S. Drop, Antonius E. van Herwaarden, Hedi L. Claahsen-van der Grinten

    Diterbitkan 2023-05-01
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  6. 6
    Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country

    Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country oleh Agustini Utari, Agustini Utari, Sultana M. H. Faradz, Annastasia Ediati, Annastasia Ediati, Tuula Rinne, Mahayu Dewi Ariani, Achmad Zulfa Juniarto, Stenvert L. S. Drop, Antonius E. van Herwaarden, Hedi L. Claahsen-van der Grinten

    Diterbitkan 2022-12-01
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  7. 7
    Androgen receptor function links human sexual dimorphism to DNA methylation.

    Androgen receptor function links human sexual dimorphism to DNA methylation. oleh Ole Ammerpohl, Susanne Bens, Mahesh Appari, Ralf Werner, Bernhard Korn, Stenvert L S Drop, Frans Verheijen, Yvonne van der Zwan, Trevor Bunch, Ieuan Hughes, Martine Cools, Felix G Riepe, Olaf Hiort, Reiner Siebert, Paul-Martin Holterhus

    Diterbitkan 2013-01-01
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  8. 8
    Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas.

    Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas. oleh Remko Hersmus, Hans Stoop, Gert Jan van de Geijn, Ronak Eini, Katharina Biermann, J Wolter Oosterhuis, Catharina Dhooge, Dominik T Schneider, Isabelle C Meijssen, Winand N M Dinjens, Hendrikus Jan Dubbink, Stenvert L S Drop, Leendert H J Looijenga

    Diterbitkan 2012-01-01
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  9. 9
    Application of the New Classification on Patients with a Disorder of Sex Development in Indonesia

    Application of the New Classification on Patients with a Disorder of Sex Development in Indonesia oleh A. Zulfa Juniarto, Yvonne G. van der Zwan, Ardy Santosa, Remko Hersmus, Frank H. de Jong, Renske Olmer, Hennie T. Bruggenwirth, Axel P. N. Themmen, Katja P. Wolffenbuttel, Leendert H. J. Looijenga, Sultana M. H. Faradz, Stenvert L. S. Drop

    Diterbitkan 2012-01-01
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  10. 10
    A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.

    A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation. oleh Remko Hersmus, Yvonne G van der Zwan, Hans Stoop, Pascal Bernard, Rajini Sreenivasan, J Wolter Oosterhuis, Hennie T Brüggenwirth, Suzan de Boer, Stefan White, Katja P Wolffenbuttel, Marielle Alders, Kenneth McElreavy, Stenvert L S Drop, Vincent R Harley, Leendert H J Looijenga

    Diterbitkan 2012-01-01
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  11. 11
    46,XX males with congenital adrenal hyperplasia: a clinical and biochemical description

    46,XX males with congenital adrenal hyperplasia: a clinical and biochemical description oleh Bas P. H. Adriaansen, Bas P. H. Adriaansen, Agustini Utari, Agustini Utari, Dineke Westra, Achmad Zulfa Juniarto, Mahayu Dewi Ariani, Annastasia Ediati, Mariska A. M. Schröder, Mariska A. M. Schröder, Paul N. Span, Fred C. G. J. Sweep, Stenvert L. S. Drop, Sultana M. H. Faradz, Antonius E. van Herwaarden, Hedi L. Claahsen – van der Grinten

    Diterbitkan 2024-08-01
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