絞り込み

16532

広告

Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?

著者 Politei J , Alberton V , Amoreo O , Antongiovanni N , Arán MN , Barán M , Cabrera G , Di Pietrantonio S , Durand C , Fainboim A , Frabasil J , Pizarro FG , Iotti R , Liern M , Perretta F , Ripeau D , Toniolo F , Trimarchi H , Rivas DV , Wallace E , Scheno
Pediatr Nephrol.2018 Jul 09 ; ():.
この記事をPubMed上で見るPubMedで表示
この記事をGoogle翻訳上で見る Google翻訳で開く

スターを付ける スターを付ける     (9view , 0users)

Full Text Sources

Fabry disease is an X-linked lysosomal storage disorder caused by α-galactosidase enzyme deficiency. We present clinical, biochemical, and histologic findings in children with classical phenotypic presentation of Fabry disease.
PMID: 29987457 [PubMed - as supplied by publisher]
印刷用ページを開く Endnote用テキストダウンロード