Literature DB >> 35997975

A rare cause of nephrotic syndrome - sphingosine-1-phosphate lyase (SGPL1) deficiency: 2 cases.

Ana Paula Spizzirri1, Carlos José Cobeñas2, Angela Del Carmen Suarez2.   

Abstract

Entities:  

Year:  2022        PMID： 35997975     DOI： 10.1007/s00467-022-05716-w

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.651


× No keyword cloud information.
  2 in total

1.  A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature.

Authors:  Tugba Tastemel Ozturk; Nur Canpolat; Seha Saygili; Umut Selda Bayrakci; Oguz Soylemezoglu; Fatih Ozaltin; Rezan Topaloglu
Journal:  Pediatr Nephrol       Date:  2022-06-24       Impact factor: 3.714

2.  MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency Syndrome.

Authors:  K W Martin; N Weaver; K Alhasan; E Gumus; B R Sullivan; M Zenker; F Hildebrandt; J D Saba
Journal:  AJNR Am J Neuroradiol       Date:  2020-08-27       Impact factor: 3.825
  2 in total
  1 in total

1.  The importance of extra-renal involvement in the hemolytic uremic syndrome.

Authors:  Sharon Phillips Andreoli
Journal:  Pediatr Nephrol       Date:  2022-06-20       Impact factor: 3.651
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.