128 related articles for article (PubMed ID: 21552011)
1. Denys-Drash syndrome and gonadoblastoma in a patient with Klinefelter syndrome.
Tanteles GA; Oakley S; Christian M; O'Neill D; Suri M
Clin Dysmorphol; 2011 Jul; 20(3):131-135. PubMed ID: 21552011
[No Abstract] [Full Text] [Related]
2. Early presentation of bilateral gonadoblastomas in a Denys-Drash syndrome patient: a cautionary tale for prophylactic gonadectomy.
Patel PR; Pappas J; Arva NC; Franklin B; Brar PC
J Pediatr Endocrinol Metab; 2013; 26(9-10):971-4. PubMed ID: 23729537
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy.
Schumacher V; Thumfart J; Drechsler M; Essayie M; Royer-Pokora B; Querfeld U; Müller D
Nephrol Dial Transplant; 2006 Feb; 21(2):518-21. PubMed ID: 16303781
[No Abstract] [Full Text] [Related]
6. Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis.
Pérez de Nanclares G; Castaño L; Bilbao JR; Vallo A; Rica I; Vela A; Martul P
J Pediatr Endocrinol Metab; 2002; 15(7):1047-50. PubMed ID: 12199335
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.
Melo KF; Martin RM; Costa EM; Carvalho FM; Jorge AA; Arnhold IJ; Mendonca BB
J Clin Endocrinol Metab; 2002 Jun; 87(6):2500-5. PubMed ID: 12050205
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Refractory Hypertension in Infantile-Onset Denys-Drash Syndrome.
Nishi K; Kamei K; Ogura M; Sato M; Murakoshi M; Kamae C; Suzuki R; Kanamori T; Nagano C; Nozu K; Ishikura K; Ito S
Tohoku J Exp Med; 2020 Sep; 252(1):45-51. PubMed ID: 32863338
[TBL] [Abstract][Full Text] [Related]
13. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome.
da Silva TE; Nishi MY; Costa EM; Martin RM; Carvalho FM; Mendonca BB; Domenice S
Pediatr Nephrol; 2011 Aug; 26(8):1311-5. PubMed ID: 21559934
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome.
Swiatecka-Urban A; Mokrzycki MH; Kaskel F; Da Silva F; Denamur E
Pediatr Nephrol; 2001 Aug; 16(8):627-30. PubMed ID: 11519891
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Denys-Drash syndrome.
Lin HC; Lin SK; Wen MC; Tseng CF; Fu LS; Chi CS
J Formos Med Assoc; 2004 Jan; 103(1):71-4. PubMed ID: 15026863
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7.
Fukuzawa R; Sakamoto J; Heathcott RW; Hata JI
J Med Genet; 2002 Aug; 39(8):e48. PubMed ID: 12161615
[No Abstract] [Full Text] [Related]
[Next] [New Search]
