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Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993
Molecular basis of aromatase deficiency in an adult female with sexual infantilism and polycystic ovariesY Ito, C R Fisher, F A Conte, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1985
Somatomedin-C levels in children and adolescents with gonadal dysgenesis: differences from age-matched normal females and effect of chronic estrogen replacement therapyL Cuttler, G Van Vliet, F A Conte, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1994
A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom)F A Conte, M M Grumbach, Y Ito, et al.
The New England Journal of Medicine|April 5, 1984
Treatment of Cushing's disease in childhood and adolescence by transsphenoidal microadenomectomyD M Styne, M M Grumbach, S L Kaplan, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1990
The pubertal growth spurt in eight patients with true precocious puberty and growth hormone deficiency: evidence for a direct role of sex steroidsK M Attie, N R Ramirez, F A Conte, et al.
Clinical Endocrinology|November 1, 1985
Congenital adrenal hyperplasia due to deficient cholesterol side-chain cleavage activity (20, 22-desmolase) in a patient treated for 18 yearsB P Hauffa, W L Miller, M M Grumbach, et al.
The Journal of Pediatrics|October 1, 1976
Delayed onset of hypopituitarism: sequelae of therapeutic irradiation of central nervous system, eye, and middle ear tumorsG E Richards, W M Wara, M M Grumbach, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1983
Endocrine, histological, and biochemical studies of adrenocorticotropin-producing islet cell carcinoma of the pancreas in childhood with characterization of proopiomelanocortinD M Styne, R Isaac, W L Miller, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1997
Idiopathic hypothalamic diabetes insipidus, pituitary stalk thickening, and the occult intracranial germinoma in children and adolescentsS L Mootha, A J Barkovich, M M Grumbach, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Normal female infants born of mothers with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiencyJ C Lo, V M Schwitzgebel, J B Tyrrell, et al.
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