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Acta Endocrinologica|June 1, 1976
Evidence for the adrenal source of androgens in precocious adrenarcheS Korth-Schutz, L S Levine, M I New
The New England Journal of Medicine|July 7, 1988
Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1P W Speiser, M I New, P C White
Endocrine Research|January 1, 1989
Clinical and genetic characterization of nonclassic 21-hydroxylase deficiencyP W Speiser, M I New, P C White
The American Journal of Cardiology|March 31, 1976
Nomograms relating aldosterone excretion to urinary sodium and potassium in the pediatric population: their application to the study of childhood hypertensionM I New, C J Baum, L S Levine
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Long term outcome in adult males with classic congenital adrenal hyperplasiaM S Cabrera, M G Vogiatzi, M I New
Acta Endocrinologica|January 1, 1978
Endocrine studies in a pubertal male pseudohermaphrodite with 17-ketosteroid reductase deficiencyR Virdis, P Saenger, B Senior, et al.
American Journal of Diseases of Children (1960)|March 1, 1981
Endocrine function in children with intrasellar and suprasellar neoplasms: before and after therapyC B Newman, L S Levine, M I New
The Journal of Clinical Endocrinology and Metabolism|January 1, 1976
Serum androgens in normal prepubertal and pubertal children and in children with precocious adrenarcheS Korth-Schutz, L S Levine, M I New
Klinische Wochenschrift|January 1, 1978
Mineralocorticoids, salt balance and blood pressure after prolonged ACTH administration in juvenile hypertensionW Rauh, L S Levine, K Gottesdiener, et al.
Human Immunology|April 1, 1986
Steroid 21-hydroxylase deficiency and the major histocompatibility complexP C White, J Werkmeister, M I New, et al.
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