128 related articles for article (PubMed ID: 35199613)
21. Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.
Köhler B; Schumacher V; Schulte-Overberg U; Biewald W; Lennert T; l'Allemand D; Royer-Pokora B; Grüters A
Pediatr Res; 1999 Feb; 45(2):187-90. PubMed ID: 10022588
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome.
Uccini S; Perotti D; Colarossi C; Stoppacciaro A; Sardella M; Mannarino O; Collini P; Casieri P; Cozzi D; Amoroso L; Spreafico F; Radice P; Dominici C
Pediatr Blood Cancer; 2008 Sep; 51(3):344-8. PubMed ID: 18293378
[TBL] [Abstract][Full Text] [Related]
24. Nephroblastic neoplasms.
Khoury JD
Clin Lab Med; 2005 Jun; 25(2):341-61, vi-vii. PubMed ID: 15848740
[TBL] [Abstract][Full Text] [Related]
25. Bilateral Nephroblastomatosis With a Unilateral Wilms Tumor: A Case Report Highlighting Imaging Characteristics.
Naggar A; Assila S; Laasri K; Andour H; Izi Z; Lamalmi N; El Haddad S; Allali N; Chat L
Glob Pediatr Health; 2024; 11():2333794X231224566. PubMed ID: 38223903
[TBL] [Abstract][Full Text] [Related]
26. Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes.
Fukuzawa R; Anaka MR; Heathcott RW; McNoe LA; Morison IM; Perlman EJ; Reeve AE
J Pathol; 2008 Aug; 215(4):377-87. PubMed ID: 18484682
[TBL] [Abstract][Full Text] [Related]
27. Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study.
Gadd S; Huff V; Huang CC; Ruteshouser EC; Dome JS; Grundy PE; Breslow N; Jennings L; Green DM; Beckwith JB; Perlman EJ
Neoplasia; 2012 Aug; 14(8):742-56. PubMed ID: 22952427
[TBL] [Abstract][Full Text] [Related]
28. The Wilms tumour (WT1) gene is mutated in a secondary leukaemia in a WAGR patient.
Pritchard-Jones K; Renshaw J; King-Underwood L
Hum Mol Genet; 1994 Sep; 3(9):1633-7. PubMed ID: 7833922
[TBL] [Abstract][Full Text] [Related]
29. Cell types expressing the Wilms' tumour gene (WT1) in Wilms' tumours: implications for tumour histogenesis.
Pritchard-Jones K; Fleming S
Oncogene; 1991 Dec; 6(12):2211-20. PubMed ID: 1722569
[TBL] [Abstract][Full Text] [Related]
30. WT1 gene analysis in sporadic early-onset and bilateral wilms tumor patients without associated abnormalities.
Perotti D; Mondini P; Terenziani M; Spreafico F; Collini P; Fossati-Bellani F; Radice P
J Pediatr Hematol Oncol; 2005 Apr; 27(4):197-201. PubMed ID: 15838390
[TBL] [Abstract][Full Text] [Related]
31. Clonality and loss of heterozygosity of WT genes are early events in the pathogenesis of nephroblastomas.
Guertl B; Ratschek M; Harms D; Jaenig U; Leuschner I; Poremba C; Hoefler G
Hum Pathol; 2003 Mar; 34(3):278-81. PubMed ID: 12673563
[TBL] [Abstract][Full Text] [Related]
32. [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]
33. Bilateral Wilms tumor. Review of outcome, associated abnormalities, and late effects in 36 pediatric patients treated at a single institution.
Shearer P; Parham DM; Fontanesi J; Kumar M; Lobe TE; Fairclough D; Douglass EC; Wilimas J
Cancer; 1993 Aug; 72(4):1422-6. PubMed ID: 8393375
[TBL] [Abstract][Full Text] [Related]
34. WT1 mutation as a cause of 46 XY DSD and Wilm's tumour: a case report and literature review.
Dai YL; Fu JF; Hong F; Xu S; Shen Z
Acta Paediatr; 2011 Jul; 100(7):e39-42. PubMed ID: 21314844
[TBL] [Abstract][Full Text] [Related]
35. Clinicopathologic features of nephrogenic rests and nephroblastomatosis.
Hennigar RA; O'Shea PA; Grattan-Smith JD
Adv Anat Pathol; 2001 Sep; 8(5):276-89. PubMed ID: 11556536
[TBL] [Abstract][Full Text] [Related]
36. Imaging Characteristics of Nephrogenic Rests Versus Small Wilms Tumors: A Report From the Children's Oncology Group Study AREN03B2.
Sandberg JK; Chi YY; Smith EA; Servaes S; Hoffer FA; Mullen EA; Perlman EJ; Tornwall B; Ehrlich PF; Geller JI; Grundy PE; Fernandez CV; Dome JS; Khanna G
AJR Am J Roentgenol; 2020 May; 214(5):987-994. PubMed ID: 32160052
[No Abstract] [Full Text] [Related]
37. Gonadoblastoma: immunohistochemical localization of Müllerian-inhibiting substance, inhibin, WT-1, and p53.
Hussong J; Crussi FG; Chou PM
Mod Pathol; 1997 Nov; 10(11):1101-5. PubMed ID: 9388060
[TBL] [Abstract][Full Text] [Related]
38. Frequency of WT1 and 11p15 constitutional aberrations and phenotypic correlation in childhood Wilms tumour patients.
Segers H; Kersseboom R; Alders M; Pieters R; Wagner A; van den Heuvel-Eibrink MM
Eur J Cancer; 2012 Nov; 48(17):3249-56. PubMed ID: 22796116
[TBL] [Abstract][Full Text] [Related]
39. WT1 microdeletion and slowly progressing focal glomerulosclerosis in a patient with male pseudohermaphroditism, childhood leukemia, Wilms tumor and cerebellar angioblastoma.
Buglyó G; Méhes G; Vargha G; Biró S; Mátyus J
Clin Nephrol; 2013 May; 79(5):414-8. PubMed ID: 23618379
[TBL] [Abstract][Full Text] [Related]
40. Aniridia, gonadoblastoma, Wilms' tumor and deletion 11p13.
Stefan H; Semecký V
Acta Medica (Hradec Kralove); 1998; 41(1):29-33. PubMed ID: 9588071
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]