Browsing by Author Castro, Margaret de

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Showing results 1 to 9 of 9
PreviewIssue DateTitleAuthor(s)AdvisorType
1-Aug-2002Bases Moleculares da Hiperplasia Adrenal CongênitaMello, Maricilda Pallandi de; Bachega, Tânia A.S.S.; Costa-Santos, Marivânia da; Mermejo, Lívia Mara; Castro, Margaret de-Artigo de periódico
1-Oct-2004Deficiência da 11beta-hidroxilaseMello, Maricilda Palandi; Penachioni, Junia Yara; Amaral, Fernando C. do; Castro, Margaret de-Artigo de periódico
1-Dec-2007Vasopressin serum levels and disorders of sodium and water balance in patients with severe brain injuryCintra, Eliane de Araújo; Araújo, Sebastião; Quagliato, Elizabeth M.A.B.; Castro, Margaret de; Falcão, Antônio Luiz Eiras; Dragosavac, Desanka; Terzi, Renato G.G.-Artigo de periódico
2007Vasopressin Serum Levels And Disorders Of Sodium And Water Balance In Patients With Severe Brain Injury.Cintra, Eliane de Araújo; Araújo, Sebastião; Quagliato, Elizabeth M A B; Castro, Margaret de; Falcão, Antônio Luiz Eiras; Dragosavac, Desanka; Terzi, Renato G G-Artigo de periódico
2004[11beta-hydroxylase Deficiency].Mello, Maricilda Palandi; Penachioni, Junia Yara; Amaral, Fernando C do; Castro, Margaret de-Artigo de periódico
2008Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive kallmann syndromeAbreu, Ana Paula; Trarbach, Ericka Barbosa; Castro, Margaret de; Costa, Elaine Maria Frade; Versiani, Beatriz; Baptista, Maria Tereza Matias; Garmes, Heraldo Mendes; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia-Artigo
2010Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1Trarbach, Ericka Barbosa; Teles, Milena Gurgel; Costa, Elaine Maria Frade; Abreu, Ana Paula; Garmes, Heraldo Mendes; Guerra, Gil; Baptista, Maria Tereza Matias; Castro, Margaret de; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia-Artigo
2009Novel mutations in CYP11B1 gene leading to 11β-Hydroxylase deficiency in brazilian patientsSoardi, Fernanda C.; Penachioni, Junia Y.; Justo, Giselle Z.; Bachega, Tânia A. S. S.; Inácio, Marlene; Mendonça, Berenice B.; Castro, Margaret de; Mello, Maricilda P. de-Artigo
2008Long‐term treatment of familial male‐limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazoleAlmeida, Madson Queiroz; Brito, Vinicius Nahime; Lins, Thereza Selma S.; Guerra-Junior, Gil; Castro, Margaret de; Antonini, Sonir Roberto; Arnhold, Ivo Jorge Prado; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia-Artigo