A novel NPHS1 mutation associated with temporary elevation of maternal serum alfa-fetoprotein and late onset of proteinuria.

Yildiz, Gizem; Torun Bayram, Meral; Soylu, Alper; Kavukçu, Salih

Yildiz, Gizem; Torun Bayram, Meral; Soylu, Alper; Kavukçu, Salih.

Afiliación

Yildiz G; Department of Pediatric Nephrology, Dokuz Eylül University Medical Faculty, Balçova, 35340, Izmir, Turkey.
Torun Bayram M; Department of Pediatric Nephrology, Dokuz Eylül University Medical Faculty, Balçova, 35340, Izmir, Turkey.
Soylu A; Department of Pediatric Nephrology and Rheumatology, Dokuz Eylül University Medical Faculty, Izmir, Turkey. alper.soylu@deu.edu.tr.
Kavukçu S; Department of Pediatric Nephrology and Rheumatology, Dokuz Eylül University Medical Faculty, Izmir, Turkey.

Int Urol Nephrol ; 53(2): 391-392, 2021 Feb.

Article en En | MEDLINE | ID: mdl-32944892

Asunto(s)

Glomeruloesclerosis Focal y Segmentaria/genética; Proteínas de la Membrana/genética; Mutación; Proteinuria/genética; alfa-Fetoproteínas/análisis; Edad de Inicio; Niño; Femenino; Humanos; Embarazo; Factores de Tiempo

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Proteinuria / Glomeruloesclerosis Focal y Segmentaria / Alfa-Fetoproteínas / Proteínas de la Membrana / Mutación Tipo de estudio: Risk_factors_studies Idioma: En Revista: Int Urol Nephrol Año: 2021 Tipo del documento: Article

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