199 related articles for article (PubMed ID: 10763762)
1. Genetics of the nephrotic syndrome.
Salomon R; Gubler MC; Niaudet P
Curr Opin Pediatr; 2000 Apr; 12(2):129-34. PubMed ID: 10763762
[TBL] [Abstract][Full Text] [Related]
2. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
Koziell A; Grech V; Hussain S; Lee G; Lenkkeri U; Tryggvason K; Scambler P
Hum Mol Genet; 2002 Feb; 11(4):379-88. PubMed ID: 11854170
[TBL] [Abstract][Full Text] [Related]
3. [The genetic basis of childhood nephrotic syndrome].
Maruniak-Chudek I; Niemir ZI; Swietliński J
Postepy Hig Med Dosw (Online); 2004; 58():405-15. PubMed ID: 15577748
[TBL] [Abstract][Full Text] [Related]
4. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
Sako M; Nakanishi K; Obana M; Yata N; Hoshii S; Takahashi S; Wada N; Takahashi Y; Kaku Y; Satomura K; Ikeda M; Honda M; Iijima K; Yoshikawa N
Kidney Int; 2005 Apr; 67(4):1248-55. PubMed ID: 15780077
[TBL] [Abstract][Full Text] [Related]
5. Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.
Patrakka J; Kestilä M; Wartiovaara J; Ruotsalainen V; Tissari P; Lenkkeri U; Männikkö M; Visapää I; Holmberg C; Rapola J; Tryggvason K; Jalanko H
Kidney Int; 2000 Sep; 58(3):972-80. PubMed ID: 10972661
[TBL] [Abstract][Full Text] [Related]
6. Genetic kidney diseases disclose the pathogenesis of proteinuria.
Jalanko H; Patrakka J; Tryggvason K; Holmberg C
Ann Med; 2001 Nov; 33(8):526-33. PubMed ID: 11730159
[TBL] [Abstract][Full Text] [Related]
7. Genetic basis of nephrotic syndrome--review.
Obeidová H; Merta M; Reiterová J; Maixnerová D; Stekrová J; Rysavá R; Tesar V
Prague Med Rep; 2006; 107(1):5-16. PubMed ID: 16752799
[TBL] [Abstract][Full Text] [Related]
8. Denys-Drash syndrome: relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1.
Coppes MJ; Huff V; Pelletier J
J Pediatr; 1993 Nov; 123(5):673-8. PubMed ID: 8229473
[No Abstract] [Full Text] [Related]
9. Expanding the spectrum of NPHS1-associated disease.
Pollak MR
Kidney Int; 2009 Dec; 76(12):1221-3. PubMed ID: 19946311
[TBL] [Abstract][Full Text] [Related]
10. Case report: Teenage girl with proteinuria and amenorrhea.
Hausladen J; Granahan E; Bockenhauer D
Curr Opin Pediatr; 2001 Apr; 13(2):150-3. PubMed ID: 11317057
[TBL] [Abstract][Full Text] [Related]
11. WT1 and glomerular diseases.
Niaudet P; Gubler MC
Pediatr Nephrol; 2006 Nov; 21(11):1653-60. PubMed ID: 16927106
[TBL] [Abstract][Full Text] [Related]
12. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
Beltcheva O; Martin P; Lenkkeri U; Tryggvason K
Hum Mutat; 2001 May; 17(5):368-73. PubMed ID: 11317351
[TBL] [Abstract][Full Text] [Related]
13. Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
Kuusniemi AM; Merenmies J; Lahdenkari AT; Holmberg C; Salmela K; Karikoski R; Rapola J; Jalanko H
Kidney Int; 2006 Oct; 70(8):1423-31. PubMed ID: 16941028
[TBL] [Abstract][Full Text] [Related]
14. Genetic basis of adult-onset nephrotic syndrome and focal segmental glomerulosclerosis.
Liu J; Wang W
Front Med; 2017 Sep; 11(3):333-339. PubMed ID: 28776307
[TBL] [Abstract][Full Text] [Related]
15. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
Franceschini N; North KE; Kopp JB; McKenzie L; Winkler C
Genet Med; 2006 Feb; 8(2):63-75. PubMed ID: 16481888
[TBL] [Abstract][Full Text] [Related]
16. Nephrotic syndrome in the 1st year of life.
Habib R
Pediatr Nephrol; 1993 Aug; 7(4):347-53. PubMed ID: 8398639
[TBL] [Abstract][Full Text] [Related]
17. Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.
Santín S; García-Maset R; Ruíz P; Giménez I; Zamora I; Peña A; Madrid A; Camacho JA; Fraga G; Sánchez-Moreno A; Cobo MA; Bernis C; Ortiz A; de Pablos AL; Pintos G; Justa ML; Hidalgo-Barquero E; Fernández-Llama P; Ballarín J; Ars E; Torra R;
Kidney Int; 2009 Dec; 76(12):1268-76. PubMed ID: 19812541
[TBL] [Abstract][Full Text] [Related]
18. Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome.
Hillen LM; Kamsteeg EJ; Schoots J; Tiebosch AT; Speel EJ; Roemen GM; Peutz-Koostra CJ; Stumpel CT
Fetal Pediatr Pathol; 2016; 35(2):112-9. PubMed ID: 26882358
[TBL] [Abstract][Full Text] [Related]
19. Molecular pathology of nephrotic syndrome in childhood: a contemporary approach to diagnosis.
Liapis H
Pediatr Dev Pathol; 2008; 11(4):154-63. PubMed ID: 18462046
[TBL] [Abstract][Full Text] [Related]
20. Molecular basis of steroid-resistant nephrotic syndrome.
Antignac C
Nefrologia; 2005; 25 Suppl 2():25-8. PubMed ID: 16050398
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
