135 related articles for article (PubMed ID: 33236617)
21. Congenital Nephrotic Syndrome of the Finnish Type in a Dominican Newborn: An Overview and Case Report.
Anderson S
Neonatal Netw; 2022 Mar; 41(2):83-88. PubMed ID: 35260424
[TBL] [Abstract][Full Text] [Related]
22. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
Guaragna MS; Cleto TL; Souza ML; Lutaif AC; de Castro LC; Penido MG; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP
Nephrology (Carlton); 2016 Sep; 21(9):753-7. PubMed ID: 26560236
[TBL] [Abstract][Full Text] [Related]
23. [Congenital nephrotic syndrome].
Hattori M
Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
[TBL] [Abstract][Full Text] [Related]
24. A novel mutation of congenital nephrotic syndrome in a Slovenian child eventually receiving a renal transplant.
Golob V; Nosan G; Bertok S; Frelih M; Boštjanči E; Rus R
Croat Med J; 2021 Apr; 62(2):187-191. PubMed ID: 33938658
[TBL] [Abstract][Full Text] [Related]
25. Novel NPHS1 splice site mutations in a Chinese child with congenital nephrotic syndrome.
Fu R; Gou MF; Ma WH; He JJ; Luan Y; Liu J
Genet Mol Res; 2015 Jan; 14(1):433-9. PubMed ID: 25729976
[TBL] [Abstract][Full Text] [Related]
26. Congenital nephrotic syndrome associated with 22q11.2 duplication syndrome in a Chinese family and functional analysis of the intronic NPHS1 c. 3286 + 5G > A mutation.
Li L; Yi Z; Xi H; Ma L; Shao H; Wang W; Pan H; Li M; Jiang H
Ital J Pediatr; 2019 Aug; 45(1):109. PubMed ID: 31443662
[TBL] [Abstract][Full Text] [Related]
27. Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry.
Hölttä T; Bonthuis M; Van Stralen KJ; Bjerre A; Topaloglu R; Ozaltin F; Holmberg C; Harambat J; Jager KJ; Schaefer F; Groothoff JW
Pediatr Nephrol; 2016 Dec; 31(12):2317-2325. PubMed ID: 27761660
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. [Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome].
Chu Y; Hou Q; Wu D; Lou G; Yang K; Guo L; Qi N; Duan X; Wang W; Qin L; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):1022-1024. PubMed ID: 31598951
[TBL] [Abstract][Full Text] [Related]
30. Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type.
Srivastava T; Garola RE; Kestila M; Tryggvason K; Ruotsalainen V; Sharma M; Savin VJ; Jalanko H; Warady BA
Pediatr Nephrol; 2006 May; 21(5):711-8. PubMed ID: 16518627
[TBL] [Abstract][Full Text] [Related]
31. Detection of the Finnish-type congenital nephrotic syndrome by restriction fragment length polymorphism and dual-color oligonucleotide ligation assays.
Romppanen EL; Mononen I
Clin Chem; 2000 Jun; 46(6 Pt 1):811-6. PubMed ID: 10839769
[TBL] [Abstract][Full Text] [Related]
32. Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
Lenkkeri U; Männikkö M; McCready P; Lamerdin J; Gribouval O; Niaudet PM; Antignac C K; Kashtan CE; Homberg C; Olsen A; Kestilä M; Tryggvason K
Am J Hum Genet; 1999 Jan; 64(1):51-61. PubMed ID: 9915943
[TBL] [Abstract][Full Text] [Related]
33. Neonatal nephrotic presentation of a child with heterozygous NPHS1 mutation.
Lemley KV
Pediatr Nephrol; 2006 Jun; 21(6):864-6. PubMed ID: 16703378
[TBL] [Abstract][Full Text] [Related]
34. Glycosaminoglycans in urine and amniotic fluid in congenital nephrotic syndrome of the Finnish type.
Ljungberg P
Pediatr Nephrol; 1994 Oct; 8(5):531-6. PubMed ID: 7818994
[TBL] [Abstract][Full Text] [Related]
35. [Changing c.106delG (p.Ala36fs*6) loss syndrome associated with congenital Finnish type: first case diagnosed in Togo].
Sabi KA; Noto-Kadou-Kaza B; Gnionsahe DA; Amekoudi EY; Tsevi CM; Tsonya KD; Amedegnato D; Gnamey K
Nephrol Ther; 2013 Dec; 9(7):494-6. PubMed ID: 23932794
[TBL] [Abstract][Full Text] [Related]
36. Congenital and infantile nephrotic syndromes.
Norio R; Rapola J
Prog Clin Biol Res; 1989; 305():179-92. PubMed ID: 2668971
[TBL] [Abstract][Full Text] [Related]
37. Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population.
Fuchshuber A; Niaudet P; Gribouval O; Jean G; Gubler MC; Broyer M; Antignac C
Pediatr Nephrol; 1996 Apr; 10(2):135-8. PubMed ID: 8703694
[TBL] [Abstract][Full Text] [Related]
38. Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: a case report.
Qiu L; Zhou J
BMC Pediatr; 2016 Mar; 16():44. PubMed ID: 27004562
[TBL] [Abstract][Full Text] [Related]
39. Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.
Kestilä M; Männikkö M; Holmberg C; Gyapay G; Weissenbach J; Savolainen ER; Peltonen L; Tryggvason K
Am J Hum Genet; 1994 May; 54(5):757-64. PubMed ID: 8178817
[TBL] [Abstract][Full Text] [Related]
40. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
Hinkes BG; Mucha B; Vlangos CN; Gbadegesin R; Liu J; Hasselbacher K; Hangan D; Ozaltin F; Zenker M; Hildebrandt F;
Pediatrics; 2007 Apr; 119(4):e907-19. PubMed ID: 17371932
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
