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Renal dysfunction is rare in Fukuyama congenital muscular dystrophy.
Ishigaki, Keiko; Kato, Ikuko; Murakami, Terumi; Sato, Takatoshi; Shichiji, Minobu; Ishiguro, Kumiko; Ishizuka, Kiyonobu; Funatsuka, Makoto; Saito, Kayoko; Osawa, Makiko; Nagata, Satoru.
Afiliación
  • Ishigaki K; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan. Electronic address: ishigaki.keiko@twmu.ac.jp.
  • Kato I; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Murakami T; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Sato T; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Shichiji M; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Ishiguro K; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Ishizuka K; Department of Pediatric Nephrology, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Funatsuka M; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Saito K; Institute of Medical Genetics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Osawa M; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Nagata S; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
Brain Dev ; 41(1): 43-49, 2019 Jan.
Article en En | MEDLINE | ID: mdl-30077507
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Walker-Warburg / Enfermedades Renales Idioma: En Revista: Brain Dev Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Walker-Warburg / Enfermedades Renales Idioma: En Revista: Brain Dev Año: 2019 Tipo del documento: Article