145 related articles for article (PubMed ID: 30914336)
1. Genetic Testing Proves Crucial in Case of Ambiguous Genitalia and Renal Masses.
Weaver J; Rove KO; Meenakshi-Sundaram B; Vricella GJ
Urology; 2019 Jul; 129():194-196. PubMed ID: 30914336
[TBL] [Abstract][Full Text] [Related]
2. A novel WT1 gene mutation in a chinese girl with denys-drash syndrome.
Wang F; Cai J; Wang J; He M; Mao J; Zhu K; Zhao M; Guan Z; Li L; Jin H; Shu Q
J Clin Lab Anal; 2021 May; 35(5):e23769. PubMed ID: 33942367
[TBL] [Abstract][Full Text] [Related]
3. Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.
Schumacher V; Schärer K; Wühl E; Altrogge H; Bonzel KE; Guschmann M; Neuhaus TJ; Pollastro RM; Kuwertz-Bröking E; Bulla M; Tondera AM; Mundel P; Helmchen U; Waldherr R; Weirich A; Royer-Pokora B
Kidney Int; 1998 Jun; 53(6):1594-600. PubMed ID: 9607189
[TBL] [Abstract][Full Text] [Related]
4. WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour.
Loirat C; André JL; Champigneulle J; Acquaviva C; Chantereau D; Bourquard R; Elion J; Denamur E
Nephrol Dial Transplant; 2003 Apr; 18(4):823-5. PubMed ID: 12637656
[No Abstract] [Full Text] [Related]
5. 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]
6. [Glomerulopathy in Denys-Drash syndrome. Case report of a model disease].
Stallmach T; Neuhaus TJ; Kösters R; Hailemariam S
Pathologe; 1998 May; 19(3):230-4. PubMed ID: 9648150
[TBL] [Abstract][Full Text] [Related]
7. A newly identified exonic mutation of the WT1 gene in a patient with Denys-Drash syndrome.
Tsuda M; Sakiyama T; Owada M; Chiba Y
Acta Paediatr Jpn; 1996 Jun; 38(3):265-6. PubMed ID: 8741319
[TBL] [Abstract][Full Text] [Related]
8. Bilateral Wilms' tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region.
Guaragna MS; Ledesma FL; Manzano VZ; Maciel-Guerra AT; Guerra-Júnior G; Silva MM; Luiz de Brito P; Palandi de Mello M
J Pediatr Endocrinol Metab; 2022 Jun; 35(6):837-843. PubMed ID: 35304980
[TBL] [Abstract][Full Text] [Related]
9. The Drash syndrome revisited: diagnosis and follow-up.
Friedman AL; Finlay JL
Am J Med Genet Suppl; 1987; 3():293-6. PubMed ID: 2835969
[TBL] [Abstract][Full Text] [Related]
10. Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort.
Sun S; Xu L; Bi Y; Wang J; Zhang Z; Tang X; Cao Q; Zhai Y; Chen J; Fang X; Liu J; Fang Y; Xiang T; Qian Y; Wu B; Wang H; Zhou W; Shen J; Dong K; Liu X; Zheng B; Zhang A; Wang X; Wu Y; Ma D; Shen Q; Rao J; Xu H
Eur J Med Genet; 2020 Nov; 63(11):104047. PubMed ID: 32891756
[TBL] [Abstract][Full Text] [Related]
11. Prophylactic bilateral nephrectomy and preemptive kidney transplantation for Denys-Drash syndrome prior to development of kidney failure.
Hosokawa C; Hotta K; Okamoto T; Cho Y; Hirose T; Iwahara N; Manabe A; Shinohara N
Pediatr Nephrol; 2024 Mar; 39(3):905-909. PubMed ID: 37572117
[TBL] [Abstract][Full Text] [Related]
12. Leukodystrophy with disorders of sex development due to WT1 mutations.
Souza PVS; Badia BML; Silva LHL; Teixeira CAC; Seneor DD; Marin VDGB; Farias IB; Dias RB; Oliveira ASB; Pinto WBVR
J Neurol Sci; 2018 Jul; 390():94-98. PubMed ID: 29801916
[TBL] [Abstract][Full Text] [Related]
13. [Urogenital malformations associated with Wilms' tumor. Molecular genetic and clinical aspects].
Zugor V; Schott GE
Urologe A; 2007 Feb; 46(2):146, 148-9. PubMed ID: 17226050
[TBL] [Abstract][Full Text] [Related]
14. Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome.
Karmila AB; Yap YC; Appadurai M; Oh L; Fazarina M; Abd Ghani F; Ariffin H
Fetal Pediatr Pathol; 2021 Apr; 40(2):113-120. PubMed ID: 31707902
[No Abstract] [Full Text] [Related]
15. Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years.
Ito S; Ikeda M; Takata A; Kikuchi H; Hata J; Honda M
Pediatr Nephrol; 1999 Nov; 13(9):790-1. PubMed ID: 10603123
[TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.
Ahn YH; Park EJ; Kang HG; Kim SH; Cho HY; Shin JI; Lee JH; Park YS; Kim KS; Ha IS; Cheong HI
Pediatr Nephrol; 2017 Jan; 32(1):81-89. PubMed ID: 27300205
[TBL] [Abstract][Full Text] [Related]
17. WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin.
Nordenskjöld A; Friedman E; Anvret M
Hum Genet; 1994 Feb; 93(2):115-20. PubMed ID: 8112732
[TBL] [Abstract][Full Text] [Related]
18. [Disorders of sex development 46 XY and bilateral metachronous wilms tumor in a child with mutation in exon 7 of WT1 gene].
Akramov NR; Osipova IV; Zakirov AK; Khaertdinov EI
Urologiia; 2019 Dec; (6):109-112. PubMed ID: 32003178
[TBL] [Abstract][Full Text] [Related]
19. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene.
Furtado LV; Pysher T; Opitz J; Lamb R; Comstock J; Batish S; Mauch T; Nelson R; Zhou H
Fetal Pediatr Pathol; 2011; 30(4):266-72. PubMed ID: 21434831
[TBL] [Abstract][Full Text] [Related]
20. Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndrome.
Devriendt K; van den Berghe K; Moerman P; Fryns JP
Prenat Diagn; 1996 May; 16(5):455-7. PubMed ID: 8844005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
