BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 22908070)

  • 21. Congenital diaphragmatic eventration with pulmonary dysplasia in Frasier syndrome due to a WT1 mutation of c.1432+5(IVS9)G>A.
    Zhang B; Ding Y; Ren X; Song C; Zhang X; Wang F; Yang X
    Eur J Med Genet; 2022 Dec; 65(12):104655. PubMed ID: 36341869
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 46,XY phenotypic male with focal segmental glomerulosclerosis caused by the WT1 splice site mutation.
    Tajima T; Sasaki S; Tanaka Y; Kusunoki H; Nagashima T; Nonomura K; Fujieda K
    Horm Res; 2003; 60(6):302-5. PubMed ID: 14646409
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical and genetic findings of five patients with WT1-related disorders.
    Andrade JG; Guaragna MS; Soardi FC; Guerra-Júnior G; Mello MP; Maciel-Guerra AT
    Arq Bras Endocrinol Metabol; 2008 Nov; 52(8):1236-43. PubMed ID: 19169475
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
    Chernin G; Vega-Warner V; Schoeb DS; Heeringa SF; Ovunc B; Saisawat P; Cleper R; Ozaltin F; Hildebrandt F;
    Clin J Am Soc Nephrol; 2010 Sep; 5(9):1655-62. PubMed ID: 20595692
    [TBL] [Abstract][Full Text] [Related]  

  • 25. WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease.
    Ferrari MTM; Watanabe A; da Silva TE; Gomes NL; Batista RL; Nishi MY; de Paula LCP; Costa EC; Costa EMF; Cukier P; Onuchic LF; Mendonca BB; Domenice S
    Sex Dev; 2022; 16(1):46-54. PubMed ID: 34392242
    [TBL] [Abstract][Full Text] [Related]  

  • 26. WT1 and glomerular diseases.
    Niaudet P; Gubler MC
    Pediatr Nephrol; 2006 Nov; 21(11):1653-60. PubMed ID: 16927106
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review.
    Anderson E; Aldridge M; Turner R; Harraway J; McManus S; Stewart A; Borzi P; Trnka P; Burke J; Coman D
    Pediatr Nephrol; 2022 Oct; 37(10):2369-2374. PubMed ID: 35211794
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Frasier syndrome: a rare syndrome with WT1 gene mutation in pediatric urology].
    Zugor V; Zenker M; Schrott KM; Schott GE
    Aktuelle Urol; 2006 Jan; 37(1):64-6. PubMed ID: 16440249
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female.
    Demmer L; Primack W; Loik V; Brown R; Therville N; McElreavey K
    J Am Soc Nephrol; 1999 Oct; 10(10):2215-8. PubMed ID: 10505699
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes).
    Auber F; Lortat-Jacob S; Sarnacki S; Jaubert F; Salomon R; Thibaud E; Jeanpierre C; Nihoul-Fékété C
    J Pediatr Surg; 2003 Jan; 38(1):124-9; discussion 124-9. PubMed ID: 12592634
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Gonadal Function in 15 Patients Associated with WT1 Gene Mutations.
    Maesaka A; Higuchi A; Kotoh S; Hasegawa Y; Ikeda M; Shishido S; Honda M
    Clin Pediatr Endocrinol; 2006; 15(4):143-9. PubMed ID: 24790335
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. 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]  

  • 35. Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome: a case report and review of the literature.
    Matsuoka D; Noda S; Kamiya M; Hidaka Y; Shimojo H; Yamada Y; Miyamoto T; Nozu K; Iijima K; Tsukaguchi H
    BMC Nephrol; 2020 Aug; 21(1):362. PubMed ID: 32838737
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Frasier syndrome: a rare cause of delayed puberty.
    Chan WK; To KF; But WM; Lee KW
    Hong Kong Med J; 2006 Jun; 12(3):225-7. PubMed ID: 16760553
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.
    Denamur E; Bocquet N; Mougenot B; Da Silva F; Martinat L; Loirat C; Elion J; Bensman A; Ronco PM
    J Am Soc Nephrol; 1999 Oct; 10(10):2219-23. PubMed ID: 10505700
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Exonic WT1 pathogenic variants in 46,XY DSD associated with gonadoblastoma.
    Arya S; Kumar S; Lila AR; Sarathi V; Memon SS; Barnabas R; Thakkar H; Patil VA; Shah NS; Bandgar TR
    Endocr Connect; 2021 Nov; 10(12):1522-1530. PubMed ID: 34727091
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Frasier Syndrome: A 15-Year-Old Phenotypically Female Adolescent Presenting with Delayed Puberty and Nephropathy.
    Shao Q; Xie X; Geng J; Yang X; Li W; Zhang Y
    Children (Basel); 2023 Mar; 10(3):. PubMed ID: 36980135
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.