201 related articles for article (PubMed ID: 16003530)
1. [Denys-Drash syndrome. Experience gathered in Erlangen illustrated by two case reports].
Zugor V; Zenker M; Dötsch J; Schrott KM; Schott GE
Urologe A; 2005 Oct; 44(10):1197-200. PubMed ID: 16003530
[TBL] [Abstract][Full Text] [Related]
2. Denys-Drash syndrome.
Kucinskas L; Rudaitis S; Pundziene B; Just W
Medicina (Kaunas); 2005; 41(2):132-4. PubMed ID: 15758579
[TBL] [Abstract][Full Text] [Related]
3. [A case of Denys-Drash syndrome with prophylactic bilateral nephrectomy].
Yamamoto K; Santo Y; Satomura K
Nihon Jinzo Gakkai Shi; 2003; 45(1):42-6. PubMed ID: 12680320
[TBL] [Abstract][Full Text] [Related]
4. Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.
Yue Z; Pei Y; Sun L; Huang W; Huang H; Hu B; Yang J; Jiang X; Mo Y; Chen S; Lai KN; Wang Y
Ren Fail; 2011; 33(9):910-4. PubMed ID: 21851196
[TBL] [Abstract][Full Text] [Related]
5. Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report.
Alge JL; Wenderfer SE; Hicks J; Bekheirnia MR; Schady DA; Kain JS; Braun MC
BMC Nephrol; 2017 Jul; 18(1):243. PubMed ID: 28720077
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.
Hakan N; Aydin M; Erdogan O; Cavusoglu YH; Aycan Z; Ozaltin F; Zenciroglu A; Apaydin S; Gunes R; Sahin G; Cinar G; Okumus N
Genet Couns; 2012; 23(2):255-61. PubMed ID: 22876585
[TBL] [Abstract][Full Text] [Related]
8. WT1 gene mutation responsible for male sex reversal and renal failure: the Frasier syndrome.
Saylam K; Simon P
Eur J Obstet Gynecol Reprod Biol; 2003 Sep; 110(1):111-3. PubMed ID: 12932885
[TBL] [Abstract][Full Text] [Related]
9. Outcome of renal transplantation for Wilms' tumor and Denys-Drash syndrome: a report of the North American Pediatric Renal Transplant Cooperative Study.
Kist-van Holthe JE; Ho PL; Stablein D; Harmon WE; Baum MA
Pediatr Transplant; 2005 Jun; 9(3):305-10. PubMed ID: 15910385
[TBL] [Abstract][Full Text] [Related]
10. [Denys-Drash syndrome].
Kohsaka T; Tagawa M; Yamada M
Nihon Rinsho; 2006 Sep; Suppl 3():457-64. PubMed ID: 17022587
[No 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. [A genetic childhood disease with consequences in adult life: the Denys-Drash syndrome].
Löwik MM; van den Berkmortel FW; Noordam C; van Hamersvelt HW; van den Heuvel LP; Levtchenko EN
Ned Tijdschr Geneeskd; 2005 Jul; 149(31):1751-5. PubMed ID: 16114294
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect.
Cho HY; Lee BS; Kang CH; Kim WH; Ha IS; Cheong HI; Choi Y
Pediatr Nephrol; 2006 Dec; 21(12):1909-12. PubMed ID: 16932893
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1.
Borel F; Barilla KC; Hamilton TB; Iskandar M; Romaniuk PJ
Biochemistry; 1996 Sep; 35(37):12070-6. PubMed ID: 8810912
[TBL] [Abstract][Full Text] [Related]
18. WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome.
Guaragna MS; Ribeiro de Andrade JG; de Freitas Carli B; Belangero VM; Maciel-Guerra AT; Guerra-Júnior G; de Mello MP
Sex Dev; 2017; 11(1):34-39. PubMed ID: 28081536
[TBL] [Abstract][Full Text] [Related]
19. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.
Heathcott RW; Morison IM; Gubler MC; Corbett R; Reeve AE
Hum Mutat; 2002 Apr; 19(4):462. PubMed ID: 11933209
[TBL] [Abstract][Full Text] [Related]
20. [Denys-Drash syndrome (DDS)].
Sasaki N
Nihon Rinsho; 2006 Jun; Suppl 2():497-8. PubMed ID: 16817450
[No Abstract] [Full Text] [Related]
[Next] [New Search]
