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Witchel, S F; Arslanian, S; Lee, P A (1999) Leptin concentrations in precocious puberty or untimely puberty with and without GnRH analogue therapy. J Pediatr Endocrinol Metab 12:839-45
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Witchel, S F; Lee, P A (1998) Human chorionic gonadotropin stimulation to assess for ovarian hyperandrogenism. J Pediatr Adolesc Gynecol 11:73-8
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Witchel, S F; Lee, P A (1998) Identification of heterozygotic carriers of 21-hydroxylase deficiency: sensitivity of ACTH stimulation tests. Am J Med Genet 76:337-42
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Witchel, S F; Lee, P A; Suda-Hartman, M et al. (1997) Hyperandrogenism and manifesting heterozygotes for 21-hydroxylase deficiency. Biochem Mol Med 62:151-8
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Witchel, S F; Wenger, S L; Hoffman, E P (1997) Molecular and cytogenetic studies of X inactivation in a patient with 46,X,del(X)(q22). J Pediatr Adolesc Gynecol 10:78-82
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Witchel, S F; Nayak, S; Suda-Hartman, M et al. (1997) Newborn screening for 21-hydroxylase deficiency: results of CYP21 molecular genetic analysis. J Pediatr 131:328-31
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Witchel, S F; Lee, P A; Suda-Hartman, M et al. (1997) Evidence for a heterozygote advantage in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Endocrinol Metab 82:2097-101
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Witchel, S F; Bhamidipati, D K; Hoffman, E P et al. (1996) Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Endocrinol Metab 81:4081-8
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Witchel, S F; Baens-Bailon, R G; Lee, P A (1996) Treatment of central precocious puberty: comparison of urinary gonadotropin excretion and gonadotropin-releasing hormone (GnRH) stimulation tests in monitoring GnRH analog therapy. J Clin Endocrinol Metab 81:1353-6
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Witchel, S S; Lee, P A; Trucco, M (1996) Who is a carrier? Detection of unsuspected mutations in 21-hydroxylase deficiency. Am J Med Genet 61:2-9
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