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Frasier Syndrome: Four New Cases With Unusual Presentations.

Guaragna, Mara Sanches; Lutaif, Anna Cristina Gervásio de Britto; Bittencourt, Viviane Barros; Piveta, Cristiane Santos Cruz; Soardi, Fernanda Caroline; Castro, Luiz Claudio Gonçalves; Belangero, Vera Maria Santoro; Maciel-Guerra, Andréa Trevas; Guerra-Junior, Gil; Mello, Maricilda Palandi De (2012)

Clinical and genetic findings of five patients with WT1-related disordersAchados clínicos e genéticos de cinco pacientes com anomalias relacionadas ao gene WT1

Andrade, Juliana Gabriel R. de; Guaragna, Mara Sanches; Soardi, Fernanda Caroline; Guerra-Júnior, Gil; Mello, Maricilda Palandi de; Maciel-Guerra, Andréa Trevas (Sociedade Brasileira de Endocrinologia e Metabologia, 2008)

Frasier Syndrome: Four New Cases With Unusual Presentations [síndrome De Frasier: Quatro Novos Casos Com Apresentação Atípica]

Guaragna M.S.; Lutaif A.C.G.B.; Bittencourt V.B.; Piveta C.S.C.; Soardi F.C.; Castro L.C.G.; Belangero V.M.S.; Maciel-Guerra A.T.; Guerra-Junior G.; de Mello M.P. (, 2012)

Frasier syndrome: four new cases with unusual presentationsSíndrome de Frasier: quatro novos casos com apresentação atípica

Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria

Guaragna, MS; Lutaif, ACGB; Piveta, CSC; Belangero, VMS; Maciel-Guerra, AT; Guerra, G; De Mello, MP (Academic Press Inc Elsevier ScienceSan DiegoEUA, 2013)

Frasier syndrome : four new cases with unusual presentations

Guaragna, Mara Sanches; Lutaif, Anna Cristina Gervásio de Britto; Bittencourt, Viviane Barros; Piveta, Cristiane Santos Cruz; Soardi, Fernanda Caroline; Castro, Luiz Claudio Gonçalves de; Belangero, Vera Maria Santoro; Maciel Guerra, Andréa Trevas; Guerra Junior, Gil; Mello, Maricilda Palandi de (Sociedade Brasileira de Endocrinologia e Metabologia, 2012-11)

A síndrome de Frasier (SF), caracterizada por disgenesia gonadal e nefropatia, é causada por mutações específicas no gene supressor do tumor de Wilms (WT1) localizado em 11p23. Pacientes com cariótipo 46,XY apresentam ...

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Frasier Syndrome: Four New Cases With Unusual Presentations.

Clinical and genetic findings of five patients with WT1-related disordersAchados clínicos e genéticos de cinco pacientes com anomalias relacionadas ao gene WT1

Frasier Syndrome: Four New Cases With Unusual Presentations [síndrome De Frasier: Quatro Novos Casos Com Apresentação Atípica]

Frasier syndrome: four new cases with unusual presentationsSíndrome de Frasier: quatro novos casos com apresentação atípica

Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria

Frasier syndrome : four new cases with unusual presentations

Two Distinct Wt1 Mutations Identified In Patients And Relatives With Isolated Nephrotic Proteinuria

Avaliação molecular do gene WT1 em pacientes pre-puberes com disgenesia gonadal parcial

Nphs2 Mutations Account For Only 15% Of Nephrotic Syndrome Cases

Two Distinct Wt1 Mutations Identified In Patients And Relatives With Isolated Nephrotic Proteinuria.

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Frasier Syndrome: Four New Cases With Unusual Presentations.

Clinical and genetic findings of five patients with WT1-related disordersAchados clínicos e genéticos de cinco pacientes com anomalias relacionadas ao gene WT1

Frasier Syndrome: Four New Cases With Unusual Presentations [síndrome De Frasier: Quatro Novos Casos Com Apresentação Atípica]

Frasier syndrome: four new cases with unusual presentationsSíndrome de Frasier: quatro novos casos com apresentação atípica

Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria

Frasier syndrome : four new cases with unusual presentations

Two Distinct Wt1 Mutations Identified In Patients And Relatives With Isolated Nephrotic Proteinuria

Avaliação molecular do gene WT1 em pacientes pre-puberes com disgenesia gonadal parcial

Nphs2 Mutations Account For Only 15% Of Nephrotic Syndrome Cases

Two Distinct Wt1 Mutations Identified In Patients And Relatives With Isolated Nephrotic Proteinuria.