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The Journal of Clinical Endocrinology and Metabolism|April 1, 1978
Prepubertal diagnosis of steroid 5 alpha-reductase deficiencyP Saenger, A S Goldman, L S Levine, et al.
The Lancet. Child & Adolescent Health|December 17, 2022
Comparative efficacy, tolerability, and acceptability of pharmacological interventions for the treatment of children, adolescents, and young adults with Tourette's syndrome: a systematic review and network meta-analysisLuis C Farhat, Emily Behling, Angeli Landeros-Weisenberger, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1979
A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisolS Ulick, L S Levine, P Gunczler, et al.
The Journal of Clinical Endocrinology and Metabolism|June 14, 2000
Osteoporosis: an unusual presentation of childhood Crohn's diseaseM Thearle, M Horlick, J P Bilezikian, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1983
HLA genotyping in family members and patients with familial polycystic ovarian diseaseF P Mandel, R J Chang, B Dupont, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1981
Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronismS E Oberfield, L S Levine, E Stoner, et al.
The New England Journal of Medicine|October 26, 1978
Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage groupL S Levine, M Zachmann, M I New, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Prepubertal girls with premature adrenarche have greater bone mineral content and density than controlsA B Sopher, J C Thornton, M E Silfen, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1982
Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasiaB Kohn, L S Levine, M S Pollack, et al.
American Journal of Human Genetics|July 1, 1981
HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyM S Pollack, L S Levine, G J O'Neill, et al.
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