Persistent Flaccid Paralysis in a Patient with Bartter Syndrome.

Krejcova, Vlasta; David, Jan; Svepes, Adam; Buksakowska, Irena; Kantorova, Eva; Liba, Zuzana; Paulas, Lukas; Indrakova, Jana; Zieg, Jakub

Krejcova, Vlasta; David, Jan; Svepes, Adam; Buksakowska, Irena; Kantorova, Eva; Liba, Zuzana; Paulas, Lukas; Indrakova, Jana; Zieg, Jakub.

Afiliación

Krejcova V; Department of Pediatrics, Motol University Hospital, Praha, Czech Republic.
David J; Department of Pediatrics, Motol University Hospital, Praha, Czech Republic.
Svepes A; Department of Pediatrics, Regional hospital Ceske Budejovice, Ceske Budejovice, Czech Republic.
Buksakowska I; Department of Radiology, Motol University Hospital, Praha, Czech Republic.
Kantorova E; Department of Medical Genetics, Regional hospital Ceske Budejovice, Ceske Budejovice, Czech Republic.
Liba Z; Department of Pediatric Neurology, Motol University Hospital, Praha, Czech Republic.
Paulas L; Department of Pediatric Neurology, Motol University Hospital, Praha, Czech Republic.
Indrakova J; Department of Medical Genetics, University Hospital Ostrava, Ostrava, Czech Republic.
Zieg J; Department of Pediatrics, Motol University Hospital, Praha, Czech Republic.

Klin Padiatr ; 235(5): 299-301, 2023 09.

Article en En | MEDLINE | ID: mdl-36848940

Asunto(s)

Síndrome de Bartter; Humanos; Síndrome de Bartter/complicaciones; Síndrome de Bartter/diagnóstico; Parálisis/diagnóstico; Parálisis/etiología; Hipotonía Muscular/diagnóstico; Hipotonía Muscular/etiología

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Bartter Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans Idioma: En Revista: Klin Padiatr Año: 2023 Tipo del documento: Article País de afiliación: República Checa Pais de publicación: Alemania

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google