273 related articles for article (PubMed ID: 16898476)
1. [The genetic background of congenital nephrotic syndrome].
Zwolińska D
Przegl Lek; 2006; 63 Suppl 3():10-1. PubMed ID: 16898476
[No Abstract] [Full Text] [Related]
2. [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]
3. Genotype-phenotype correlations: filling the void.
Parsa A
Clin J Am Soc Nephrol; 2010 Sep; 5(9):1542-3. PubMed ID: 20724521
[No Abstract] [Full Text] [Related]
4. Genetic forms of nephrotic syndrome: a single-center experience in Brussels.
Ismaili K; Pawtowski A; Boyer O; Wissing KM; Janssen F; Hall M
Pediatr Nephrol; 2009 Feb; 24(2):287-94. PubMed ID: 18709391
[TBL] [Abstract][Full Text] [Related]
5. [WT1 mutation as a cause of progressive nephropathy in Frasier syndrome--case report].
Wasilewska A; Zoch-Zwierz W; Tenderenda E; Rybi-Szumińska A; Kołodziejczyk Z
Pol Merkur Lekarski; 2009 Jun; 26(156):642-4. PubMed ID: 19711733
[TBL] [Abstract][Full Text] [Related]
6. [Congenital nephrotic syndrome].
Hattori M
Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
[TBL] [Abstract][Full Text] [Related]
7. Expanding the clinical spectrum of Frasier syndrome.
Gwin K; Cajaiba MM; Caminoa-Lizarralde A; Picazo ML; Nistal M; Reyes-Múgica M
Pediatr Dev Pathol; 2008; 11(2):122-7. PubMed ID: 17378674
[TBL] [Abstract][Full Text] [Related]
8. Renal transplantation in small children with congenital nephrotic syndrome of the Finnish type.
Holmberg C; Jalanko H; Koskimies O; Leijala M; Salmela K; Eklund B; Ahonen J
Transplant Proc; 1991 Feb; 23(1 Pt 2):1378-9. PubMed ID: 1989242
[No Abstract] [Full Text] [Related]
9. Different clinical presentations of WT1 gene mutations.
Aydin M; Hakan N; Zenciroglu A; Aydog O; Okumus N
Eur J Pediatr; 2013 Dec; 172(12):1705-6. PubMed ID: 23835858
[No Abstract] [Full Text] [Related]
10. [Congenital and infantile nephrotic syndrome].
Niaudet P
Nephrol Ther; 2005 Mar; 1(1):63-70. PubMed ID: 16895669
[TBL] [Abstract][Full Text] [Related]
11. Patients with different or identical genotypes of the WT1 gene present different phenotypes.
Yang Y; Zhao F; Huang J; Nie X; Yu Z
Eur J Pediatr; 2013 Dec; 172(12):1707-8. PubMed ID: 23835859
[No Abstract] [Full Text] [Related]
12. WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes.
Aucella F; Bisceglia L; De Bonis P; Gigante M; Caridi G; Barbano G; Mattioli G; Perfumo F; Gesualdo L; Ghiggeri GM
Pediatr Nephrol; 2006 Oct; 21(10):1393-8. PubMed ID: 16909243
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Detailed clinical manifestations at onset and prognosis of neonatal-onset Denys-Drash syndrome and congenital nephrotic syndrome of the Finnish type.
Nishi K; Inoguchi T; Kamei K; Hamada R; Hataya H; Ogura M; Sato M; Yoshioka T; Ogata K; Ito S; Nakanishi K; Nozu K; Hamasaki Y; Ishikura K
Clin Exp Nephrol; 2019 Aug; 23(8):1058-1065. PubMed ID: 30963316
[TBL] [Abstract][Full Text] [Related]
15. Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome.
Chiang PW; Aliaga S; Travers S; Spector E; Tsai AC
Curr Opin Pediatr; 2008 Feb; 20(1):103-6. PubMed ID: 18197048
[TBL] [Abstract][Full Text] [Related]
16. [Congenital nephrotic syndrome].
Bilinska W; Rogowska-Kalisz A; Puczko-Nogal B; Nowicki M
Med Wieku Rozwoj; 2002; 6(2):89-98. PubMed ID: 12426454
[TBL] [Abstract][Full Text] [Related]
17. Two cases of congenital nephrotic syndrome.
Iitaka K; Motoyama O; Hojo M; Iwanami N; Koshino H; Nakamura S; Moriya S
Clin Exp Nephrol; 2004 Jun; 8(2):146-9. PubMed ID: 15235932
[TBL] [Abstract][Full Text] [Related]
18. A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male.
Yang Y; Feng D; Huang J; Nie X; Yu Z
Eur J Pediatr; 2013 Jan; 172(1):127-9. PubMed ID: 22763603
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Successful transplantation in a child with rapid progression of autosomal recessive polycystic kidney disease associated with a novel mutation.
Prelog M; Bergmann C; Ausserlechner MJ; Fischer H; Margreiter R; Gassner I; Brunner A; Jungraithmayr TC; Zerres K; Sergi C; Zimmerhackl LB
Pediatr Transplant; 2006 May; 10(3):362-6. PubMed ID: 16677362
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]