Pang, Songya

Genotyping steroid 21-hydroxylase deficiency: hormonal reference data

NEW, M. I., LORENZEN, F., LERNER, A. J., KOHN, B., OBERFIELD, S. E., POLLACK, M. S., DUPONT, B., STONER, E., LEVY, D. J., PANG, S., et al. (1983) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 624

Worldwide Experience in Newborn Screening for Classical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Pang, S., Wallace, M. A., Hofman, L., Thuline, H. C., Dorche, C., Lyon, I. C. T., Dobbins, R. H., Kling, S., Fujieda, K., & Suwa, S. (1988) · Journal of Urology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 392

Late-onset adrenal steroid 3β-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women

PANG, S., LERNER, A. J., STONER, E., LEVINE, L. S., OBERFIELD, S. E., ENGEL, I., & NEW, M. I. (1985) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 238

Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia

KOHN, B., LEVINE, L. S., POLLACK, M. S., PANG, S., LORENZEN, F., LEVY, D., LERNER, A. J., RONDANINI, G. F., DUPONT, B., & NEW, M. I. (1982) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 204

Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing

Pollack, M. S., Levine, L. S., Pang, S., Owens, R. P., Nitowsky, H. M., Dupont, B., Maurer, D., New, M. I., Duchon, M., Merkatz, I. R., et al. (1979) · The Lancet

Sexual Differentiation and DisordersPrenatal Screening and Diagnostics

Cited by 126

Nonsalt-losing congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency with normal glomerulosa function

Pang, S., Levine, L. S., Stoner, E., Opitz, J. M., Pollack, M. S., Dupont, B., & New, M. I. (1983) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 112

Current status of neonatal screening for congenital adrenal hyperplasia

Pang, S., & Shook, M. K. (1997) · Current Opinion in Pediatrics

Sexual Differentiation and DisordersMetabolism and Genetic Disorders

Cited by 104

Genetic and Hormonal Characterization of Cryptic 21-Hydroxylase Deficiency*

LEVINE, L. S., DUPONT, B., LORENZEN, F., PANG, S., POLLACK, M., OBERFIELD, S. E., KOHN, B., LERNER, A., CACCIARI, E., MANTERO, F., et al. (1981) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 81

Inherited congenital adrenal hyperplasia in the rabbit is caused by a deletion in the gene encoding cytochrome P450 cholesterol side-chain cleavage enzyme

Yang, X., Iwamoto, K., Wang, M., Artwohl, J., Mason, J. I., & Pang, S. (1993) · Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 73

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 adrenal 3β-HSD activity

Chang, Y. T., Zhang, L. I., Alkaddour, H. S., Mason, J. I., Lin, K., Yang, X., Garibaldi, L. R., Bourdony, C. J., Dolan, L. M., Donaldson, D. L., et al. (1995) · Pediatric Research

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 65

Mutations in the Type II 3β-Hydroxysteroid Dehydrogenase Gene in a Patient with Classic Salt-Wasting 3β-Hydroxysteroid Dehydrogenase Deficiency Congenital Adrenal Hyperplasia

Chang, Y. T., Kappy, M. S., Iwamoto, K., Wang, J., Yang, X., & Pang, S. (1993) · Pediatric Research

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 44

Extra-adrenal induction of Cyp21a1 ameliorates systemic steroid metabolism in a mouse model of congenital adrenal hyperplasia

Naiki, Y., Miyado, M., Horikawa, R., Katsumata, N., Onodera, M., Pang, S., Ogata, T., & Fukami, M. (2016) · Endocrine Journal

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 40

Carriers for type II 3β‐hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test

Pang, S., Carbunaru, G., Haider, A., Copeland, K. C., Chang, Y. T., Lutfallah, C., & Mason, J. I. (2003) · Clinical Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 24