Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients von Varela, MC, Kok, F, Setian, N, Kim, CA, Koiffmann, CP

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Inhibin A Production after Gonadotropin Stimulus: A New Method to Detect Ovarian Tissue in Ovotesticular Disorder of Sex Development von Steinmetz, L., Rocha, M.N., Longui, C.A., Damiani, D., Dichtchekenian, V., Setian, N., Damiani, D.

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Hypophosphatemic rickets and osteomalacia due to a parathyroid adenoma: A case-report von Menezes-Filho, H.C, Portela, L.G, Banwart, K.J, Fuks, F, Montenegro, F.L, Steinmetz, L, Della Manna, T, Kuperman, H, Dichtchekenian, V, Setian, N, Damiani, D

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Evaluation of the effects of disodium pamidronate on the serum lipid profile in pediatric patients with severe Osteogenesis Imperfecta von Menezes-Filho, H.C, Radonsky, V, Colares-Neto, G.P, Kuperman, H, Della anna, T, Dichtchekenian, V, Setian, N, Damiani, D

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Decrease of Serum Alkaline Phosphatase after Three Cycles of Pamidronate Disodium in Children with Severe Osteogenesis Imperfecta von Cabral de Menezes Filho, H., Rodrigues, J.M., Radonsky, V., Della Manna, T., Kuperman, H., Steinmetz, L., Dichtchekenian, V., Damiani, D., Setian, N.

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Subcutaneous Use of a Fast-Acting Insulin Analog: An alternative treatment for pediatric patients with diabetic ketoacidosis von Della Manna, Thais, Steinmetz, Leandra, Campos, Paula R, Farhat, Sylvia C.L, Schvartsman, Cláudio, Kuperman, Hilton, Setian, Nuvarte, Damiani, Durval

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Severe Hypercalcemia in a 9-Year-Old Brazilian Girl Due to a Novel Inactivating Mutation of the Calcium-Sensing Receptor von Miyashiro, Kozue, Kunii, Ilda, Manna, Thais Della, de Menezes Filho, Hamilton C., Damiani, Durval, Setian, Nuvarte, Hauache, Omar M.

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Evaluation of the hypothalamic-pituitary-adrenal axis in children with leukemia before and after 6 weeks of high-dose glucocorticoid therapy von KUPERMAN, Hilton, DAMIANI, Durval, CHROUSOS, George P, DICHTCHEKENIAN, Vaê, DELLA MANNA, Thais, ODONE, Vicente FILHO, SETIAN, Nuvarte

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Identification and functional analysis of a novel inactivating mutation (A804D) of the calcium-sensing receptor gene von Miyashiro, Kozue, Kasamatsu, Teresa Sayoko, Steinmetz, Leandra, De Menezes Filho, Hamilton Cabral, Damiani, Durval, Setian, Nuvarte, Hauache, Omar Magid

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True hermaphroditism: clinical aspects and molecular studies in 16 cases von DAMIANI, D, FELLOUS, M, MCELREAVEY, K, BARBAUX, S, BARRETO, E. S. A, DICHTCHEKENIAN, V, SETIAN, N

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CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency von WITCHEL, S. F, SMITH, R, CRIVELLARO, C. E, DELLA MANNA, T, DICHTCHEKENIAN, V, SETIAN, N, DAMIANI, D

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Correlation of pathologic features with clinical outcome in pediatric adrenocortical neoplasia : a study of a Brazilian population von BUGG, M. F, RIBEIRO, R. C, ROBERSON, P. K, LLOYD, R. V, SANDRINI, R, SILVA, J. B, EPELMAN, S, SHAPIRO, D. N, PARHAM, D. M

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Rathke's cleft cyst as a cause of growth hormone deficiency and micropenis von SETIAN, N, AGUIAR, C. H, GALVAO, J. A, CRIVELLARO, C. E, DICHTCHEKENIAN, V, DAMIANI, D

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Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: Delineation of a newly recognized overgrowth syndrome von Moretti-Ferreira, Danilo, Koiffmann, Célia P., Listik, Márcia, Setian, Nuvarte, Wajntal, Anita

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Thyroid carcinoma in children and adolescents - review of six cases von Damiani, D, Dichtchekenian, V, Setian, N, Szeliga, D V, Passos, L D, Lima, T M, Manna, T D, Kuperman, H

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26 PSYCHOLOGICAL STUDY IN PRECOCIOUS PUBERTY von Rotenberg, L, Setian, N

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Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome von Damiani, D, Billerbeck, A E, Goldberg, A C, Setian, N, Fellous, M, Kalil, J

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Characterization of GH secretory ability of GH deficient children: Response to MK-0677 von Yu, H, Arango, A, Bercu, B, Bach, MA, Cassorla, F, DiMartino, J, Kanojia, P, Kletter, G, Krupa, D, Pescovitz, O, Setian, N, Shi, Y-F, Tiulpakov, A

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34 THYROID HORMONES IN MALNOURISHED CHILDREN von Setian, N, Pupo, A A

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Investigations of the ZFY gene in XX true hermaphroditism and Swyer syndrome von DAMIANI, D, BILLERBECK, A. E. C, GOLDBERG, A. C. K, SETIAN, N, FELLOUS, M, KALIL, J

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