166 related articles for article (PubMed ID: 31587616)
1. Gastric duplication cyst in an infant with Finnish-type congenital nephrotic syndrome: concurrence or coincidence?
Güngör T; Eroğlu FK; Kargın Çakıcı E; Yazılıtaş F; Can G; Çelikkaya E; Karakaya D; Kurt Şükür ED; Özaltın F; Yağız B; Bülbül M
Acta Clin Belg; 2021 Apr; 76(2):155-157. PubMed ID: 31587616
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation.
Uysal B; Dönmez O; Uysal F; Akacı O; Vuruşkan BA; Berdeli A
Pediatr Int; 2015; 57(1):177-9. PubMed ID: 25711261
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish type.
Lee BH; Ahn YH; Choi HJ; Kang HK; Kim SD; Cho BS; Moon KC; Ha IS; Cheong HI; Choi Y
J Korean Med Sci; 2009 Jan; 24 Suppl(Suppl 1):S210-4. PubMed ID: 19194555
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Congenital nephrotic syndrome of the Finnish type--key to the mechanisms of proteinuria].
Holmberg C; Jalanko H
Duodecim; 2011; 127(10):1017-25. PubMed ID: 21696001
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Congenital Nephrotic Syndrome - Finish Type.
Spahiu L; Merovci B; Jashari H; Këpuska AB; Rugova BE
Med Arch; 2016 Jun; 70(3):232-4. PubMed ID: 27594755
[TBL] [Abstract][Full Text] [Related]
11. Mutations in NPHS1 in a Chinese child with congenital nephrotic syndrome.
Yu ZH; Wang DJ; Meng DC; Huang J; Nie XJ
Genet Mol Res; 2012 May; 11(2):1460-4. PubMed ID: 22653594
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.
Patrakka J; Ruotsalainen V; Reponen P; Qvist E; Laine J; Holmberg C; Tryggvason K; Jalanko H
Transplantation; 2002 Feb; 73(3):394-403. PubMed ID: 11884936
[TBL] [Abstract][Full Text] [Related]
14. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
Machuca E; Benoit G; Nevo F; Tête MJ; Gribouval O; Pawtowski A; Brandström P; Loirat C; Niaudet P; Gubler MC; Antignac C
J Am Soc Nephrol; 2010 Jul; 21(7):1209-17. PubMed ID: 20507940
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Congenital nephrotic syndrome with a novel NPHS1 mutation.
Yoshizawa C; Kobayashi Y; Ikeuchi Y; Tashiro M; Kakegawa S; Watanabe T; Goto Y; Nakanishi K; Yoshikawa N; Arakawa H
Pediatr Int; 2016 Nov; 58(11):1211-1215. PubMed ID: 27882743
[TBL] [Abstract][Full Text] [Related]
17. Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation.
Holmberg C; Jalanko H
Pediatr Nephrol; 2014 Dec; 29(12):2309-17. PubMed ID: 24682440
[TBL] [Abstract][Full Text] [Related]
18. Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1).
Kuusniemi AM; Qvist E; Sun Y; Patrakka J; Rönnholm K; Karikoski R; Jalanko H
Transplantation; 2007 May; 83(10):1316-23. PubMed ID: 17519780
[TBL] [Abstract][Full Text] [Related]
19. [Congenital nephrotic syndrome].
Hattori M
Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
[TBL] [Abstract][Full Text] [Related]
20. [A Case of Congenital Nephrotic Syndrome of the Finnish Type].
Zhou Y; Chen Q; Huang X; Yang LM; Chen J
Sichuan Da Xue Xue Bao Yi Xue Ban; 2020 Nov; 51(6):881-884. PubMed ID: 33236617
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]