Hypothyroidism in children: diagnosis and treatment by Setian, Nuvarte Setian

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Hipotireoidismo na criança: diagnóstico e tratamento by Setian, Nuvarte

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Hipotireoidismo na criança: diagnóstico e tratamento Hypothyroidism in children: diagnosis and treatment by Nuvarte Setian

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

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Hipotireoidismo na criança: diagnóstico e tratamento by Setian, Nuvarte

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Severe Hypercalcemia in a 9-Year-Old Brazilian Girl Due to a Novel Inactivating Mutation of the Calcium-Sensing Receptor by 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 by Kuperman, Hilton, Damiani, Durval, Chrousos, George P., Dichtchekenian, Vaê, Manna, Thais Della, Filho, Vicente Odone, Setian, Nuvarte

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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 by 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 by Miyashiro, Kozue, Kasamatsu, Teresa Sayoko, Steinmetz, Leandra, De Menezes Filho, Hamilton Cabral, Damiani, Durval, Setian, Nuvarte, Hauache, Omar Magid

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Premature thelarche: identification of clinical and laboratory data for the diagnosis of precocious puberty by Della Manna, Thais, Setian, Nuvarte, Damiani, Durval, Kuperman, Hilton, Dichtchekenian, Vaê

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Carcinoma de tireóide em crianças e adolescentes - revisão de seis casos by Szeliga, Daniela V. M., Setian, Nuvarte, Passos, Leonardo D., Lima, Thais M. R., Manna, Thais Della, Kuperman, Hilton, Damiani, Durval, Dichtchekenian, Vaê

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

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Carcinoma de tireóide em crianças e adolescentes - revisão de seis casos by Szeliga, Daniela V. M., Setian, Nuvarte, Passos, Leonardo D., Lima, Thais M. R., Manna, Thais Della, Kuperman, Hilton, Damiani, Durval, Dichtchekenian, Vaê

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Cystic fibrosis-related diabetes: a frequent co-morbidity by Della Manna, Thais, Setian, Nuvarte, Rodrigues, Joaquim Carlos

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A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism by Battistin, Claudilene, Menezes Filho, Hamilton Cabral de, Domenice, Sorahia, Nishi, Mirian Yumie, Della Manna, Thais, Kuperman, Hilton, Steinmetz, Leandra, Dichtchekenian, Vaê, Setian, Nuvarte, Damiani, Durval

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Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities by Filho, Hamilton Cabral de Menezes, Marui, Suemi, Manna, Thais Della, Brust, Ester Saraiva, Radonsky, Vanessa, Kuperman, Hilton, Dichtchekenian, Vaê, Setian, Nuvarte, Damiani, Durval

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O diabetes melito na fibrose cística: uma comorbidade cada vez mais freqüente by Della Manna, Thais, Setian, Nuvarte, Rodrigues, Joaquim Carlos

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Iodo radioativo no tratamento de portadores de doença de Graves by Setian, Nuvarte

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Altura final após tratamento com cetoconazol em meninos portadores de puberdade precoce familial by Setian, Nuvarte

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Crianças tratadas com o hormônio de crescimento by Setian, Nuvarte

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