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The International Journal of Pediatric Nephrology|October 1, 1985
Evaluation of percutaneous transluminal renal angioplasty in childhood hypertensionF Fallo, S E Oberfield, L S Levine, et al.Clinical and Experimental Hypertension. Part A, Theory and Practice|January 1, 1986
Percutaneous transluminal renal angioplasty in the treatment of renovascular hypertension in childrenF Fallo, S E Oberfield, L S Levine, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature reviewM E Damore, P W Speiser, A E Slonim, et al.The Journal of Clinical Endocrinology and Metabolism|September 16, 1999
Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitaliaB I Cerame, R S Newfield, L Pascoe, et al.The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutationsS Nimkarn, B I Cerame, J Q Wei, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|December 28, 2012
Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 geneO Lekarev, K Tafuri, A H Lane, 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 Investigation|August 1, 1992
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP W Speiser, J Dupont, D Zhu, 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.Pageof 21