AAAAAA

   
Results: 1-15 |
Results: 15
Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
Authors: Speiser, PW
Citation: Pw. Speiser, Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency, END METAB C, 30(1), 2001, pp. 31
Congenital adrenal hyperplasia - Preface
Authors: Speiser, PW
Citation: Pw. Speiser, Congenital adrenal hyperplasia - Preface, END METAB C, 30(1), 2001, pp. XI-XII
Congenital adrenal hyperplasia: Transition from childhood to adulthood
Authors: Speiser, PW
Citation: Pw. Speiser, Congenital adrenal hyperplasia: Transition from childhood to adulthood, J ENDOC INV, 24(9), 2001, pp. 681-691
Profiles of obese children presenting for metabolic evaluation
Authors: Anavian, J Brenner, DJ Fort, P Speiser, PW
Citation: J. Anavian et al., Profiles of obese children presenting for metabolic evaluation, J PED END M, 14(8), 2001, pp. 1145-1150
A multicenter study of women with nonclassical congenital adrenal hyperplasia: Relationship between genotype and phenotype
Authors: Speiser, PW Knochenhauer, ES Dewailly, D Fruzzetti, F Marcondes, JAM Azziz, R
Citation: Pw. Speiser et al., A multicenter study of women with nonclassical congenital adrenal hyperplasia: Relationship between genotype and phenotype, MOL GEN MET, 71(3), 2000, pp. 527-534
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (vol 21, pg 245, 2000)
Authors: White, PC Speiser, PW
Citation: Pc. White et Pw. Speiser, Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (vol 21, pg 245, 2000), ENDOCR REV, 21(5), 2000, pp. 550-550
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Authors: White, PC Speiser, PW
Citation: Pc. White et Pw. Speiser, Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, ENDOCR REV, 21(3), 2000, pp. 245-291
Ovarian hyperthecosis in the setting of portal hypertension
Authors: Speiser, PW Susin, M Sasano, H Bohrer, S Markowitz, J
Citation: Pw. Speiser et al., Ovarian hyperthecosis in the setting of portal hypertension, J CLIN END, 85(2), 2000, pp. 873-877
21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study
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
Distinct missense mutations of the FCFR3 Lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype
Authors: Bellus, GA Spector, EB Speiser, PW Weaver, CA Garber, AT Bryke, CR Israel, J Rosengren, SS Webster, MK Donoghue, DJ Francomano, CA
Citation: Ga. Bellus et al., Distinct missense mutations of the FCFR3 Lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype, AM J HU GEN, 67(6), 2000, pp. 1411-1421
Regulation of HSD17B1 and SRD5A1 in lymphocytes
Authors: Zhou, ZF Speiser, PW
Citation: Zf. Zhou et Pw. Speiser, Regulation of HSD17B1 and SRD5A1 in lymphocytes, MOL GEN MET, 68(3), 1999, pp. 410-417
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: Patient report and literature review
Authors: Damore, ME Speiser, PW Slonim, AE New, MI Shanske, S Xia, WL Santorelli, FM DiMauro, S
Citation: Me. Damore et al., Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: Patient report and literature review, J PED END M, 12(2), 1999, pp. 207-213
Toward better treatment of congenital adrenal hyperplasia
Authors: Speiser, PW
Citation: Pw. Speiser, Toward better treatment of congenital adrenal hyperplasia, CLIN ENDOCR, 51(3), 1999, pp. 273-274
Prenatal treatment of congenital adrenal hyperplasia
Authors: Speiser, PW
Citation: Pw. Speiser, Prenatal treatment of congenital adrenal hyperplasia, J UROL, 162(2), 1999, pp. 534-536
Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific genein neonatal screening for congenital adrenal hyperplasia
Authors: Fitness, J Dixit, N Webster, D Torresani, T Pergolizzi, R Speiser, PW Day, DJ
Citation: J. Fitness et al., Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific genein neonatal screening for congenital adrenal hyperplasia, J CLIN END, 84(3), 1999, pp. 960-966
Risultati: 1-15 |