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Literature DB >> 14978189

Podocin and nephrotic syndrome: implications for the clinician.

Patrick Niaudet.

Abstract

Entities: Disease Gene

Mesh：

Substances：

Year: 2004 PMID： 14978189 DOI： 10.1097/01.asn.0000118135.00519.b0

Source DB: PubMed Journal: J Am Soc Nephrol ISSN： 1046-6673 Impact factor: 10.121

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Cited

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9 in total

Review 1. Treatment of steroid-resistant nephrotic syndrome in the genomic era.

Authors: Adam R Bensimhon; Anna E Williams; Rasheed A Gbadegesin
Journal: Pediatr Nephrol Date: 2018-10-02 Impact factor: 3.714

2. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.

Authors: Afig Berdeli; Sevgi Mir; Onder Yavascan; Erkin Serdaroglu; Mustafa Bak; Nejat Aksu; Ayse Oner; Ali Anarat; Osman Donmez; Nurhan Yildiz; Lale Sever; Yilmaz Tabel; Ruhan Dusunsel; Ferah Sonmez; Nilgun Cakar
Journal: Pediatr Nephrol Date: 2007-09-25 Impact factor: 3.714

3. Genetic forms of nephrotic syndrome: a single-center experience in Brussels.

Authors: Khalid Ismaili; Audrey Pawtowski; Olivia Boyer; Karl Martin Wissing; Françoise Janssen; Michelle Hall
Journal: Pediatr Nephrol Date: 2008-08-16 Impact factor: 3.714

4. Electronic microarray screening of podocin mutations: a single-center study.

Authors: Onur Sakallioglu; Faysal Gok; Suleyman Kalman; Davut Gul; Hande Barutcu; Nurcan Cengiz; Esra Baskin
Journal: Int Urol Nephrol Date: 2008-08-06 Impact factor: 2.370

5. NPHS2 variation in sporadic focal segmental glomerulosclerosis.

Authors: Louise M McKenzie; Sher L Hendrickson; William A Briggs; Richard A Dart; Stephen M Korbet; Michelle H Mokrzycki; Paul L Kimmel; Tejinder S Ahuja; Jeffrey S Berns; Eric E Simon; Michael C Smith; Howard Trachtman; Donna M Michel; Jeffrey R Schelling; Monique Cho; Yu C Zhou; Elizabeth Binns-Roemer; Gregory D Kirk; Jeffrey B Kopp; Cheryl A Winkler
Journal: J Am Soc Nephrol Date: 2007-10-17 Impact factor: 10.121

Podocin and nephrotic syndrome: implications for the clinician.

Review 1. Treatment of steroid-resistant nephrotic syndrome in the genomic era.

2. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.

3. Genetic forms of nephrotic syndrome: a single-center experience in Brussels.

4. Electronic microarray screening of podocin mutations: a single-center study.

5. NPHS2 variation in sporadic focal segmental glomerulosclerosis.

Review 6. Analysis of the clinical characteristics of arthritis with renal disease caused by a NPHS2 gene mutation.

7. New perspectives on the renal slit diaphragm protein podocin.

8. Progress in pathogenesis of proteinuria.

9. Association Between NPHS2 p.R229Q and Focal Segmental Glomerular Sclerosis/Steroid-Resistant Nephrotic Syndrome.