Proteinuria and progressive kidney failure due to an inborn error of metabolism: Answers.


Uzun Ö., Cengiz N., Çavdarlı B., Bayrakçı U., Kiremitçi S., Yavaş A. K.

Pediatric nephrology (Berlin, Germany), vol.36, pp.2055-2058, 2021 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 36
  • Publication Date: 2021
  • Doi Number: 10.1007/s00467-020-04901-z
  • Journal Name: Pediatric nephrology (Berlin, Germany)
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, CINAHL, EMBASE, MEDLINE, Veterinary Science Database
  • Page Numbers: pp.2055-2058
  • Keywords: Child, Dysostosis multiplex, Kidney disease, Cherry-red spot, Nephrosialidosis, Lysosomal storage disorder, NEU1 mutation, NEURAMINIDASE DEFICIENCY, SIALIDOSIS
  • Kocaeli University Affiliated: Yes