Extra-adrenal induction of Cyp21a1 ameliorates systemic steroid metabolism in a mouse model of congenital adrenal hyperplasia von Naiki, Yasuhiro, Miyado, Mami, Horikawa, Reiko, Katsumata, Noriyuki, Onodera, Masafumi, Pang, Songya, Ogata, Tsutomu, Fukami, Maki

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Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita von REUTENS, A. T, ACHERMANN, J. C, ITO, Masafumi, ITO, Mika, GU, W.-X, HABIBY, R. L, DONOHOUE, P. A, SONGYA PANG, HINDMARSH, P. C, JAMESON, J. L

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Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression von ACHERMANNT, John C, ITO, Masafumi, SILVERMAN, Bernard L, HABIBY, Reema L, SONGYA PANG, ROSLER, Ariel, JAMESON, J. Larry

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The Molecular and Clinical Spectrum of 3β-hydroxysteroid Dehydrogenase Deficiency Disorder von Pang, Songya

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Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3β-hydroxysteroid dehydrogenase (3βHSD) gene causing, respectively, nonsalt-wasting... von LI ZHANG, MASON, J. I, NAIKI, Y, COPELAND, K. C, CASTRO-MAGANA, M, GORDON-WALKER, T. T, CHANG, Y. T, SONGYA PANG

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Newborn screening, prenatal diagnosis, and prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency von Pang, Songya, Clark, Anastasia

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Absence of molecular defect in the type II 3β-hydroxysteroid dehydrogenase (3β-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrena... von CHANG, Y. T, LI ZHANG, SONGYA PANG, ALKADDOUR, H. S, MASON, J. I, KEMMING LIN, XIAOJIANG YANG, GARIBALDI, L. R, BOURDONY, C. J, DOLAN, L. M, DONALDSON, D. L

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Steroidogenic Enzyme Gene Expression in Androgen Induced Polycystic Ovaries in the Rabbit von Iwamoto, Kotaro, Mason, J. Ian, Manaligod, Jose, Pau, K-Y Francis, Spies, Harold G., Pang, Songya

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Diet-hormone interactions: Protein/carbohydrate ratio alters reciprocally the plasma levels of testosterone and cortisol and their respective binding globulins in man von Anderson, Karl E., Rosner, William, Khan, M.S., New, Maria I., Pang, Songya, Wissel, Paul S., Kappas, Attallah

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The Hormonal Phenotype of Nonclassic 3β-Hydroxysteroid Dehydrogenase (HSD3B) Deficiency in Hyperandrogenic Females Is Associated with Insulin-Resistant Polycystic Ovary Syndrome an... von Carbunaru, Goldy, Prasad, Pallavi, Scoccia, Bert, Shea, Patrick, Hopwood, Nancy, Ziai, Fuad, Chang, Ying Tai, Myers, Susan E., Mason, J. Ian, Pang, Songya

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Current status of neonatal screening for congenital adrenal hyperplasia von Pang, S, Shook, M K

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Comparison of adrenocorticotropin and adrenal steroid responses to corticotropin-releasing hormone versus metyrapone testing in patients with hypopituitarism von RIDDICK, L, CHROUSOS, G. P, JEFFRIES, S, SONGYA PANG

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The Effect of Three Menstrual Cycle Phases on Adrenal Hormonal Dynamics and Etiologies of Hirsutism in Five Ethnic/Racial Female Populations von Sakkal-Alkaddour, Hala, Jean Suriano, Mary, Riddick, Linda, T. Chang, Ying, Ziai, Fuad, Pang, Songya

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Carriers for type II 3(beta)-hydroxysterioid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test von Pang, Songya, Goldy Carbunaru, Haider, Anzar, Copeland, Kenneth C

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Hirsutism, Polycystic Ovarian Disease, and Ovarian 17-Ketosteroid Reductase Deficiency von Pang, Songya, Softness, Barney, Sweeney, William J, New, Maria I

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Carriers for type II 3β-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test von Pang, Songya, Carbunaru, Goldy, Haider, Anzar, Copeland, Kenneth C., Chang, Ying Tai, Lutfallah, Chantal, Mason, J. Ian

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Clinical, Hormonal, and Radiological Studies at Baseline, During and After Long Term GnRH Analog (Leuprolide) Treatment in Adolescent Hirsute Females with Increased Ovarian Androge... von Tai Chang, Ying, Jean Suriano, Mary, Garibaldi, Luigi, Riddick, Linda, Pang, Songya

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Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency von SONGYA PANG, WALLACE, M. A, HOFMAN, L, THULINE, H. C, DORCHE, C, LYON, I. C. T, DOBBINS, R. H, KLING, S, FUJIEDA, K, SUWA, S

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Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test von Pang, Songya, Carbunaru, Goldy, Haider, Anzar, Copeland, Kenneth C, Chang, Ying Tai, Lutfallah, Chantal, Mason, J Ian

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Missense Mutations Cluster within the Carboxyl-Terminal Region of DAX-1 and Impair Transcriptional Repression1 von Achermann, John C., Ito, Masafumi, Silverman, Bernard L., Habiby, Reema L., Pang, Songya, Rosler, Ariel, Jameson, J. Larry

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