Molecular Basis of Aromatase Deficiency in an Adult Female with Sexual Infantilism and Polycystic Ovaries von Ito, Yuji, Fisher, Carolyn R., Conte, Felix A., Grumbach, Melvin M., Simpson, Evan R.

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Endocrine and neurologic outcome in childhood craniopharyngioma: Review of effect of treatment in 42 patients von Thomsett, M.J., Conte, F.A., Kaplan, S.L., Grumbach, M.M.

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The Role of Estrogen in the Male and Female: Evidence from Mutations in Synthesis and Action von Grumbach, M.M.

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Acute N-Methyl-D,L-Aspartate Administration Stimulates the Luteinizing Hormone Releasing Hormone Pulse Generator in the Ovine Fetus von Bettendorf, M., de Zegher, F., Albers, N., Hart, C.S., Kaplan, S.L., Grumbach, M.M.

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SEPTO-OPTIC DYSPLASIA AND PITUITARY DWARFISM von Hoyt, W.F, Kaplan, S.L, Grumbach, M.M, Glaser, J.S

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Ontogenesis of fetal endocrine function von Kaplan, S.L., Grumbach, M.M.

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Bovine somatotropin and the safety of cows' milk: National Institutes of Health Technology Assessment Conference statement von Grumbach M.M, Bier D.M, Blumenthal H, Clark J. Jr, Dunkley W.L, Gray G.M, Hintz R.L, Hutton N.E, Knobil E, Lippe B

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Reply von Lovinger, R.D., Kaplan, S.L., Grumbach, M.M.

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Prolactin in umbilical cord blood and the respiratory distress syndrome von Gluckman, P.D., Ballard, P.L., Kaplan, S.L., Liggins, G.C., Grumbach, M.M.

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Alpha melanocyte stimulating hormone inhibits prolactin secretion in fetal and infant lambs von Gluckman, Peter D., Marti-Henneberg, Carlos, Leisti, Seppo, Kaplan, Selna L., Grumbach, Melvin M.

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Hypopituitarism after irradiation in children von Wara, William M., Richards, Gail E., Grumbach, Melvin M., Kaplan, Selna L., Sheline, Glenn E., Conte, Felix A.

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Growth hormone secretion in cachexia von Conte, F.A., Kaplan, S.L., Abrams, C.A.L., Grumbach, M.M.

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Serum growth hormone response to insulin-induced hypoglycemia in disorders of growth von Kaplan, S.L., Abrams, C.A.L., Bell, J.J., Conte, F.A., Grumbach, M.M.

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A calcified aldosterone-producing tumor in a hypertensive, normokalemic, prepubertal girl von Kelch, R.P., Connors, M.H., Kaplan, S.L., Biglieri, E.G., Grumbach, M.M.

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O.10 Mutations in a new dynein/dynactin adaptor gene cause Dominant Congenital Spinal Muscular Atrophy (DCSMA) and Hereditary Spastic Paraplegia (HSP) von Oates, E.C, Rosser, A.M, Hafezparast, M, Lek, M, Scoto, M, Greensmith, L, Auer-Grumbach, M, Schule, R, Herrmann, D.N, Clarke, N.F, MacArthur, D.G, Züchner, S, Muntoni, F, Reilly, M.M, North, K.N

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