The origin of urinary mulberry cells in Fabry disease.

Yokoyama, Takashi; Manabe, Shun; Horita, Shigeru; Kataoka, Hiroshi; Mochizuki, Toshio; Nitta, Kosaku

Yokoyama, Takashi; Manabe, Shun; Horita, Shigeru; Kataoka, Hiroshi; Mochizuki, Toshio; Nitta, Kosaku.

Afiliação

Yokoyama T; Department of Clinical Laboratory Medicine, Tokyo Women's Medical University Hospital, Tokyo, Japan.
Manabe S; Department of Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Horita S; Department of Clinical Laboratory Medicine, Tokyo Women's Medical University Hospital, Tokyo, Japan.
Kataoka H; Department of Nephrology, Tokyo Women's Medical University, Tokyo, Japan; Clinical Research Division for Polycystic Kidney Disease, Department of Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Mochizuki T; Department of Nephrology, Tokyo Women's Medical University, Tokyo, Japan; Clinical Research Division for Polycystic Kidney Disease, Department of Nephrology, Tokyo Women's Medical University, Tokyo, Japan. Electronic address: mtoshi@twmu.ac.jp.
Nitta K; Department of Nephrology, Tokyo Women's Medical University, Tokyo, Japan.

Kidney Int ; 99(5): 1246, 2021 05.

Article em En | MEDLINE | ID: mdl-33892869

Assuntos

Doença de Fabry; Nefropatias; Morus; Doença de Fabry/genética; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Fabry / Morus / Nefropatias Limite: Humans Idioma: En Revista: Kidney Int Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão

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