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Results: 1-15 |
Results: 15

Authors: Lewy, VD Danadian, K Witchel, SF Arslanian, S
Citation: Vd. Lewy et al., Early metabolic abnormalities in adolescent girls with polycystic ovarian syndrome, J PEDIAT, 138(1), 2001, pp. 38-44

Authors: Witchel, SF White, C Seigel, ME Aston, CE
Citation: Sf. Witchel et al., Inconsistent effects of the proline(12) -> alanine variant of the peroxisome proliferator-activated receptor-gamma 2 gene on body mass index in children and adolescent girls, FERT STERIL, 76(4), 2001, pp. 741-747

Authors: Witchel, SF Smith, R Tomboc, M Aston, CE
Citation: Sf. Witchel et al., Candidate gene analysis in premature pubarche and adolescent hyperandrogenism, FERT STERIL, 75(4), 2001, pp. 724-730

Authors: Witchel, SF Smith, R Crivellaro, CE Della Manna, T Dichtchekenian, V Setian, N Damiani, D
Citation: Sf. Witchel et al., CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency, HUM GENET, 106(4), 2000, pp. 414-419

Authors: Witchel, SF Aston, CE
Citation: Sf. Witchel et Ce. Aston, The role of heterozygosity for CYP21 in the polycystic ovary syndrome, J PED END M, 13, 2000, pp. 1315-1317

Authors: Tomboc, M Lee, PA Mitwally, MF Schneck, FX Bellinger, M Witchel, SF
Citation: M. Tomboc et al., Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism, J CLIN END, 85(11), 2000, pp. 4013-4018

Authors: Kahsar-Miller, M Azziz, R Feingold, E Witchel, SF
Citation: M. Kahsar-miller et al., A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome, FERT STERIL, 74(6), 2000, pp. 1237-1240

Authors: Witchel, SF Fagerli, J Siegel, J Smith, R Mitwally, MF Lewy, V Arslanian, S Lee, PA
Citation: Sf. Witchel et al., No association between body mass index and beta(3)-adrenergic receptor variant (W64R) in children with premature pubarche and adolescent girls with hyperandrogenism, FERT STERIL, 73(3), 2000, pp. 509-515

Authors: Moran, C Azziz, R Carmina, E Dewailly, D Fruzzetti, F Ibanez, L Knochenhauer, ES Marcondes, JAM Mendonca, BB Pignatelli, D Pugeat, M Rohmer, V Speiser, PW Witchel, SF
Citation: C. Moran et al., 21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study, AM J OBST G, 183(6), 2000, pp. 1468-1474

Authors: Witchel, SF Smith, RR
Citation: Sf. Witchel et Rr. Smith, Glucocorticoid resistance in premature pubarche and adolescent hyperandrogenism, MOL GEN MET, 66(2), 1999, pp. 137-141

Authors: Witchel, SF
Citation: Sf. Witchel, Molecular diagnosis in the congenital adrenal hyperplasias, ENDOCRINOLO, 9(3), 1999, pp. 197-207

Authors: Witchel, SF Arslanian, S Lee, PA
Citation: Sf. Witchel et al., Leptin concentrations in precocious puberty or untimely puberty with and without GnRH analogue therapy, J PED END M, 12(6), 1999, pp. 839-845

Authors: Witchel, SF Arslanian, S
Citation: Sf. Witchel et S. Arslanian, Ovarian responses to hCG stimulation: insulin resistance/hyperinsulinaemiavs. insulin deficiency, CLIN ENDOCR, 51(1), 1999, pp. 127-130

Authors: Escobar-Morreale, HF San Millan, JL Smith, RR Sancho, J Witchel, SF
Citation: Hf. Escobar-morreale et al., The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations, FERT STERIL, 72(4), 1999, pp. 629-638

Authors: Fagerli, J Schneck, FX Lee, PA Bellinger, MF Witchel, SF
Citation: J. Fagerli et al., Absence of microdeletions in the Y chromosome in patients with a history of cryptorchidism and azoospermia or oligospermia, FERT STERIL, 71(4), 1999, pp. 697-700
Risultati: 1-15 |