Literature DB >> 35997973

Response to Dr. Spizzirri et al.

Tugba Tastemel Ozturk1, Fatih Ozaltin2,3, Rezan Topaloglu2.   

Abstract

Entities:  

Year:  2022        PMID： 35997973     DOI： 10.1007/s00467-022-05717-9

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


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  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

Review 2.  Expert consensus guidelines for the genetic diagnosis of Alport syndrome.

Authors:  Judy Savige; Francesca Ariani; Francesca Mari; Mirella Bruttini; Alessandra Renieri; Oliver Gross; Constantinos Deltas; Frances Flinter; Jie Ding; Daniel P Gale; Mato Nagel; Michael Yau; Lev Shagam; Roser Torra; Elisabet Ars; Julia Hoefele; Guido Garosi; Helen Storey
Journal:  Pediatr Nephrol       Date:  2018-07-09       Impact factor: 3.714
  2 in total

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