Search Results - "Chang, Ying Tai"

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

“…Summary objective We investigated adrenal steroidogenic function relevant to 3β‐hydroxysteroid dehydrogenase (HSD3B2) activity in vivo and HSD3B2 genotype in…”
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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 and Is Not a Variant of Inherited HSD3B2 Deficiency by Carbunaru, Goldy, Prasad, Pallavi, Scoccia, Bert, Shea, Patrick, Hopwood, Nancy, Ziai, Fuad, Chang, Ying Tai, Myers, Susan E., Mason, J. Ian, Pang, Songya

“…To test our hypothesis that the hormonal phenotype of mild 3β-hydroxysteroid dehydrogenase (HSD3B) deficiency in hyperandrogenic females (HF) is related to…”
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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 Androgen Production Due to Polycystic Ovary Syndrome by Tai Chang, Ying, Jean Suriano, Mary, Garibaldi, Luigi, Riddick, Linda, Pang, Songya

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Hypothalamic-pituitary-gonadal axis function in pubertal male and female siblings with glucocorticoid-treated nonsalt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia by Chang, Y T, Kulin, H E, Garibaldi, L, Suriano, M J, Bracki, K, Pang, S

“…We report pubertal maturation and dynamic studies of gonadotropin and gonadal hormone secretion in long term glucocorticoid-treated siblings with…”
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Molecular genetics of human androgen insensitivity by Brown, T R, Scherer, P A, Chang, Y T, Migeon, C J, Ghirri, P, Murono, K, Zhou, Z

“…Androgen insensitivity syndromes represent one cause of human male pseudohermaphroditism related to defects in the androgen receptor. The formation of a…”
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Early Detection of Alzheimer's Disease Through Eye Movement Analysis: A Digital Diagnostic Approach by Lin, Yu-chun, Huang, Li-kai, Wu, Jeng-chian, Chang, Tai-ying, Hu, Hsiang-Wei

“…Given the increasing worldwide incidence of dementia, primarily Alzheimer's disease dementia, there is an urgent requirement for non-invasive, early diagnostic…”
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Hypocalcemia in nonwhite breast-fed infants. Vitamin D deficiency revisited by Chang, Y T, Germain-Lee, E L, Doran, T F, Migeon, C J, Levine, M A, Berkovitz, G D

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Binding of methyltrienolone to androgen receptors in human skin fibroblasts is enhanced by insulin by Chang, Y. T, Ghirri, P, Migeon, C. J, Brown, T. R

“…Previous reports have suggested a relationship between hyperinsulinemia and increased androgen secretion leading to female virilization, but no report has been…”
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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 by Pang, Songya, Carbunaru, Goldy, Haider, Anzar, Copeland, Kenneth C, Chang, Ying Tai, Lutfallah, Chantal, Mason, J Ian

“…We investigated adrenal steroidogenic function relevant to 3beta-hydroxysteroid dehydrogenase (HSD3B2) activity in vivo and HSD3B2 genotype in clinically…”
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A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia by Pang, Songya, Wang, Weihua, Rich, Barry, David, Raphael, Chang, Ying Tai, Carbunaru, Goldy, Myers, Susan E, Howie, A Forbes, Smillie, Karen J, Mason, J Ian

“…We investigated two novel point mutations in the human type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing a mild and a severe form of…”
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Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency by Lutfallah, Chantal, Wang, Weihua, Mason, J Ian, Chang, Ying Tai, Haider, Anzar, Rich, Barry, Castro-Magana, Mariano, Copeland, Kenneth C, David, Raphael, Pang, Songya

“…To define the hormonal criteria via genotypic proof for 3beta-hydroxysteroid dehydrogenase (3beta-HSD) deficiency in the adrenals and gonads, we investigated…”
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A Novel Nonstop Mutation in the Stop Codon and a Novel Missense Mutation in the Type II 3β-Hydroxysteroid Dehydrogenase (3β-HSD) Gene Causing, Respectively, Nonclassic and Classic 3β-HSD Deficiency Congenital Adrenal Hyperplasia by Pang, Songya, Wang, Weihua, Rich, Barry, David, Raphael, Chang, Ying Tai, Carbunaru, Goldy, Myers, Susan E., Howie, A. Forbes, Smillie, Karen J., Mason, J. Ian

“…We investigated two novel point mutations in the human type II 3β-hydroxysteroid dehydrogenase (3β-HSD) gene causing a mild and a severe form of 3β-HSD…”
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Newly Proposed Hormonal Criteria via Genotypic Proof for Type II 3β-Hydroxysteroid Dehydrogenase Deficiency by Lutfallah, Chantal, Wang, Weihua, Mason, J. Ian, Chang, Ying Tai, Haider, Anzar, Rich, Barry, Castro-Magana, Mariano, Copeland, Kenneth C., David, Raphael, Pang, Songya

“…To define the hormonal criteria via genotypic proof for 3β-hydroxysteroid dehydrogenase (3β-HSD) deficiency in the adrenals and gonads, we investigated the…”
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Newly proposed hormonal criteria via genotypic proof for type II 3β-hydroxysteroid dehydrogenase deficiency : The impact of the human genome on endocrinology: Special features by LUTFALLAH, Chantal, WEIHUA WANG, MASON, J. Ian, YING TAI CHANG, HAIDER, Anzar, RICH, Barry, CASTRO-MAGANA, Mariano, COPELAND, Kenneth C, DAVID, Raphael, SONGYA PANG

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A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3β-hydroxysteroid dehydrogenase (3β-HSD) gene causing, respectively, nonclassic and classic 3β-HSD deficiency congenital adrenal hyperplasia : The impact of the human genome on endocrinology: Special features by PANG, Songya, WEIHUA WANG, RICH, Barry, DAVID, Raphael, YING TAI CHANG, CARBUNARU, Goldy, MYERS, Susan E, HOWIE, A. Forbes, SMILLIE, Karen J, MASON, J. Ian

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Which patient factors trigger a diagnosis of atypical childhood diabetes? by Baumann, Elizabeth E, Cashin, Kathy, Chang, Ying-Tai, Duck, Stephen, Edidin, Deborah, Lipton, Rebecca B

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Molecular basis of congenital adrenal hyperplasia in two siblings with classical nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency by Rhéaume, E, Sanchez, R, Simard, J, Chang, Y T, Wang, J, Pang, S, Labrie, F

“…We report mutations of the type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) gene in two siblings, male and female, with congenital adrenal hyperplasia…”
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Mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene in a patient with classic salt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia by Chang, Y T, Kappy, M S, Iwamoto, K, Wang, J, Yang, X, Pang, S

“…Inherited adrenal and gonadal 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency is most likely caused by a mutation of the type II 3 beta-HSD gene…”
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