Browsing by Author Mello, Maricilda P. de

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Showing results 1 to 8 of 8
PreviewIssue DateTitleAuthor(s)AdvisorType
1-Dec-2012Prevalência de anormalidades genitais em recém-nascidosMonlleó, Isabella L.; Zanotti, Susane V.; Araújo, Bárbara Priscila B. de; Cavalcante Júnior, Erisvaldo F.; Pereira, Paula D.; Barros, Paulo M. de; Araújo, Maria Deysiane P.; Mendonça, Ana Thaysa V. S. de; Santos, Catarina R. S.; Santos, Ylana R. dos; Michelatto, Débora de Paula; Mello, Maricilda P. de; Maciel-Guerra, Andrea T.; Guerra-Júnior, Gil-Artigo de periódico
2009T allele of-344C/T polymorphism in aldosterone synthase gene is not associated with resistant hypertensionLacchini, Riccardo; Sabha, Maricene; Coeli, Fernanda B.; Favero, Fabrício F.; Yugar-Toledo, Juan; Izidoro-Toledo, Tatiane C.; Sandrim, Valéria C.; Tanus-Santos, José E.; Mello, Maricilda P. de; Moreno, Heitor-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
2016Nr5a1 Loss-of-function mutations lead to 46,xy partial gonadal dysgenesis phenotype: report of three novel mutationsFabbri, Helena C.; Ribeiro de Andrade, Juliana G.; Maciel-Guerra, Andrea T.; Guerra Junior, Gil; Mello, Maricilda P. de-Artigo
2017Wt1 haploinsufficiency supports milder renal manifestation in two patients with denys-drash syndromeGuaragna, Mara S.; Andrade, Juliana G. Ribeiro de; Carli, Barbara de Freitas; Belangero, Vera M. S.; Maciel-Guerra, Andrea T.; Guerra -Junior, Gil; Mello, Maricilda P. de-Outros documentos
2015Nphs2 mutations account for only 15% of nephrotic syndrome casesGuaragna, Mara Sanches; Souza, Marcela L.; Lutaif, Anna Cristina G. B.; Piveta, Cristiane S. C.; Mello, Maricilda P. de; Belangero, Vera M. S.; Henriques, Taciane B.; Guerra-Junior, Gil; Maciel-Guerra, Andréa T.; Souza, Suéllen R. de-Artigo
2016Nphs1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: a novel mutation is describedGuaragna, Mara S.; Guerra-Junior, Gil; Mello, Maricilda P. de; Maciel-Guerra, Andréa T.; Penido, Maria Goretti Moreira Guimarães; Castro, Luiz Cláudio Gonçalves de; Souza, Marcela Lopes; Lutaif, Anna Cristina G. B.; Cleto, Thaís Lira; Belangero, Vera M. S.-Artigo
2017Functional impact of novel androgen receptor mutations on the clinical manifestation of androgen insensitivity syndromePetroli, Reginaldo J.; Hiort, Olaf; Struve, Dagmar; Gesing, Julia K.; Soardi, Fernanda C.; Spinola-Castro, Angela M.; Melo, Karla; Arnhold, Ivo J. Prado; Maciel-Guerra, Andrea T.; Guerra-Junior, Gil; Werner, Ralf; Mello, Maricilda P. de-Artigo