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The Journal of Clinical Endocrinology and Metabolism|December 1, 1976
Presence of H-Y antigen and testis in 46, XX true hermaphroditism, evidence for Y-chromosomal functionP Saenger, L S Levine, S S Wachtel, et al.Journal of Pediatric Hematology/Oncology|February 24, 2001
Primary central nervous system lymphoma in childhood presenting as progressive panhypopituitarismM E Silfen, J H Garvin, A P Hays, et al.The Journal of Clinical Endocrinology and Metabolism|January 1, 1991
3 alpha-Androstanediol glucuronide in premature and normal pubarcheL M Riddick, L R Garibaldi, M E Wang, et al.Lancet (London, England)|May 26, 1979
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typingM S Pollack, D Maurer, L S Levine, et al.The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Genotyping steroid 21-hydroxylase deficiency: hormonal reference dataM I New, F Lorenzen, A J Lerner, et al.Journal of Child and Adolescent Psychopharmacology|December 4, 2019
Measuring Treatment Response in Pediatric Trichotillomania: A Meta-Analysis of Clinical TrialsLuis C Farhat, Emily Olfson, Jessica L S Levine, et al.Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.Journal of Psychiatric Research|April 10, 2024
An evaluation of treatment response and remission definitions in adult obsessive-compulsive disorder: A systematic review and individual-patient data meta-analysisDivya Ramakrishnan, Luis C Farhat, Edoardo F Q Vattimo, et al.Pageof 12