Výsledky vyhledávání - "Claude J. Migeon"

Publikováno v: eLS. :1-9

In human subjects, the sex chromosomes are the X and the Y chromosomes. Normally, a complement of two X chromosomes (46,XX) is seen in females and one X and one Y (46,XY) in males. The X-chromosome includes about 1500 genes, only a few of which are i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1d22adc28e13524270473eecf63caa1
https://doi.org/10.1002/9780470015902.a0005943.pub2

Zobrazit plný text záznamu

Review and management of 46,XY Disorders of Sex Development

Autor: Heather DiCarlo, Claude J. Migeon, John P. Gearhart, Eric Z. Massanyi

Publikováno v: Journal of Pediatric Urology. 9:368-379

Disorders of Sex Development (DSD) among 46,XY individuals are rare and challenging conditions. Abnormalities of karyotype, gonadal formation, androgen synthesis, and androgen action are responsible for the multiple disorders that result in underviri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e2f0f1096f80c8934bf298af640f95
https://doi.org/10.1016/j.jpurol.2012.12.002

Zobrazit plný text záznamu

Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development

Autor: Elizabeth E. Squibb, Nancy Braverman, George H. Thomas, Claude J. Migeon, Veronica Mardo, Denise A.S. Batista, Julie Hoover-Fong

Publikováno v: American Journal of Medical Genetics Part A. :2293-2297

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ff4d8494d6f310239824b63f4bd9f8d
https://doi.org/10.1002/ajmg.a.32316

Zobrazit plný text záznamu

Temporal and individual variations in the dose of glucocorticoid used for the treatment of salt-losing congenital virilizing adrenal hyperplasia due to 21-hydroxylase deficiency

Autor: R Sandrini, Claude J. Migeon, Nicholas Jospe

Publikováno v: Acta Paediatrica. 82:56-60

The dose of glucocorticoid was evaluated in the treatment of 19 patients with salt-losing congenital adrenal hyperplasia due to complete or nearly complete 21-hydroxylase deficiency. In most cases, follow-up was from infancy to puberty. The dose of s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba160221f4d6fc1d8c31df5063fd5c99
https://doi.org/10.1111/j.1651-2227.1993.tb12844.x

Zobrazit plný text záznamu

Summary of consensus statement on intersex disorders and their management

Autor: Olaf Hiort, Polly Carmichael, Leendert H. J. Looijenga, John C. Achermann, Norman P. Spack, Ute Thyen, Claude J. Migeon, Sylvano Bertelloni, Erica A. Eugster, John W. Brock, Vincent R. Harley, Jay N. Giedd, Kenneth J. Zucker, Peggy T. Cohen-Kettenis, Jean D. Wilson, Peter A. Lee, Justine M. Schober, Eric Vilain, William G. Reiner, Anna Nordenström, Melvin Grumbach, Kenji Fujieda, Paul Saenger, Pierre Mouriquand, Chris Driver, Hertha Richter-Appelt, Felix A. Conte, Patricia A. Donohoue, Robert Rapaport, Ken Copeland, Barbara Thomas, Emilie F. Rissman, Christopher P. Houk, Bernadice Mendoca, Garry L. Warne, Laurence S. Baskin, Christopher Woodhouse, Sheri A. Berenbaum, Stenvert L. S. Drop, S Faisal Ahmed, Ieuan A. Hughes, Yves Morel, Heino F. L. Meyer-Bahlburg, Cheryl Chase, David E. Sandberg, Amy B. Wisniewski, Melissa Hines, Richard C. Rink, P.G. Ransley

Publikováno v: Houk, C P, Hughes, I A, Ahmed, S F, Lee, P A, Hiort, O, Vilain, E, Hines, M, Berenbaum, S, Copeland, K, Donohoue, P, Baskin, L, Mouriquand, P, Meyer-Bahlburg, H, Carmichael, P, Drop, S, Warne, G, Achermann, J, Eugster, E, Harley, V, Morel, Y, Rapaport, R, Wilson, J, Cohen-Kettenis, P, Giedd, J, Nordenström, A, Reiner, W, Rissman, E, Bertelloni, S, Conte, F, Migeon, C, Driver, C, Fujieda, K, Brock, J, Grumbach, M, Ransley, P, Rink, R, Woodhouse, C, Richter-Appelt, H, Sandberg, D, Spack, N, Thomas, B, Zucker, K, Looijenga, L, Mendoca, B, Saenger, P, Schober, J, Thyen, U, Wisniewski, A & Chase, C 2006, ' Summary of consensus statement on intersex disorders and their management ', Pediatrics, vol. 118, no. 2, pp. 753-757 . https://doi.org/10.1542/peds.2006-0737
Pediatrics, 118(2), 753-757. American Academy of Pediatrics

Advances in understanding of genetic control of sexual determination and differentiation, improvements in diagnostic testing and surgical genital repair, and the persistent controversies inherent to clinical management were all compelling factors tha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1924b253c302681f685abcc584bbced9
http://www.scopus.com/inward/record.url?scp=33748422544&partnerID=8YFLogxK

Zobrazit plný text záznamu

Long-Term Corticosteroid Replacement and Bone Mineral Density in Adult Women with Classical Congenital Adrenal Hyperplasia

Autor: Amy B. Wisniewski, Brandon Bankowski, Claude J. Migeon, Jeremy A. King, Kathryn A. Carson, Howard A. Zacur

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 91:865-869

Context: Concern has been raised regarding the potential impact of chronic glucocorticoid therapy on the bone mineral density (BMD) of patients with congenital adrenal hyperplasia (CAH). Objective: The purpose of this investigation was to assess the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49dff25e0e9a3e7d5051ad7293cb2545
https://doi.org/10.1210/jc.2005-0745

Zobrazit plný text záznamu

PSYCHOSEXUAL OUTCOME IN WOMEN AFFECTED BY CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

Autor: John P. Gearhart, Matthew A. Malouf, Claude J. Migeon, Amy B. Wisniewski

Publikováno v: Journal of Urology. 171:2497-2501

Purpose: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency results in increased adrenal androgen secretion. When the deficiency is severe, the result is the salt losing (SL) form, and when the deficiency is partial, the result is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b562aef7bfb73778786fce38dcc8fd
https://doi.org/10.1097/01.ju.0000125269.91938.f7

Zobrazit plný text záznamu

Long-Term Perspectives for 46,XY Patients Affected by Complete Androgen Insensitivity Syndrome or Congenital Micropenis

Autor: Amy B. Wisniewski, Claude J. Migeon

Publikováno v: Seminars in Reproductive Medicine. 20:297-304

Controversy concerning optimal treatment for individuals affected by syndromes of abnormal sex differentiation can best be resolved with knowledge about long-term medical, surgical, and psychosexual outcomes of patients. Follow-up information has rec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2fd104d98bffdf0825fe657930ef8b2
https://doi.org/10.1055/s-2002-35376

Zobrazit plný text záznamu

Lawson Wilkins and my life: part 3

Autor: Claude J. Migeon

Publikováno v: International Journal of Pediatric Endocrinology

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97dc6dd6872fc3387b9ad76381c8d34d
https://pubmed.ncbi.nlm.nih.gov/25024715

Zobrazit plný text záznamu

CONGENITAL ADRENAL HYPERPLASIA OWING TO 21-HYDROXYLASE DEFICIENCY

Autor: Amy B. Wisniewski, Claude J. Migeon

Publikováno v: Endocrinology and Metabolism Clinics of North America. 30:193-206

In the absence of long-term results of experimental therapies, a common sense approach toward dealing with the growth of patients who have CAH is desirable. First, an effort can be made to decrease the replacement cortisol dose during the first year

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::03c0f260eff01fa8788c97b6fe475c69
https://doi.org/10.1016/s0889-8529(08)70026-4

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání