BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 17101338)

  • 1. Prophylactic bilateral salpingo-oopherectomy in a 17-year-old with Frasier syndrome reveals gonadoblastoma and seminoma: a case report.
    Love JD; DeMartini SD; Coppola CP
    J Pediatr Surg; 2006 Nov; 41(11):e1-4. PubMed ID: 17101338
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
    Barbaux S; Niaudet P; Gubler MC; Grünfeld JP; Jaubert F; Kuttenn F; Fékété CN; Souleyreau-Therville N; Thibaud E; Fellous M; McElreavey K
    Nat Genet; 1997 Dec; 17(4):467-70. PubMed ID: 9398852
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome.
    Subbiah V; Huff V; Wolff JE; Ketonen L; Lang FF; Stewart J; Langford L; Herzog CE
    Pediatr Blood Cancer; 2009 Dec; 53(7):1349-51. PubMed ID: 19653292
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expanding the clinical spectrum of Frasier syndrome.
    Gwin K; Cajaiba MM; Caminoa-Lizarralde A; Picazo ML; Nistal M; Reyes-Múgica M
    Pediatr Dev Pathol; 2008; 11(2):122-7. PubMed ID: 17378674
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Frasier syndrome: early gonadoblastoma and cyclosporine responsiveness.
    Sinha A; Sharma S; Gulati A; Sharma A; Agarwala S; Hari P; Bagga A
    Pediatr Nephrol; 2010 Oct; 25(10):2171-4. PubMed ID: 20419325
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frasier syndrome in a pre-menarchal girl: laparoscopic resection of gonadoblastoma.
    Saxena AK; van Tuil C; Schultze-Everding A
    Eur J Pediatr; 2006 Dec; 165(12):917-9. PubMed ID: 16915373
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gonadoblastoma and dysgerminoma associated with XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome.
    Joki-Erkkilä MM; Karikoski R; Rantala I; Lenko HL; Visakorpi T; Heinonen PK
    J Pediatr Adolesc Gynecol; 2002 Jun; 15(3):145-9. PubMed ID: 12106750
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Laparoscopically Removed Streak Gonad Revealed Gonadoblastoma in Frasier Syndrome.
    Hashimoto K; Horibe YU; Ezaki J; Kanno T; Takahashi N; Akizawa Y; Matsui H; Yamamoto T; Shibata N
    Anticancer Res; 2017 Jul; 37(7):3975-3979. PubMed ID: 28668903
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 46 XY pure gonadal dysgenesis with gonadoblastoma and dysgerminoma.
    Ben Temime R; Chachial A; Attial L; Ghodbanel I; Makhloufl T; Koubaal A; Kourda N; Ben Jilani S; Dammak T; El May A; Rahal K
    Tunis Med; 2008 Jul; 86(7):710-3. PubMed ID: 19472738
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation.
    Kitsiou-Tzeli S; Deligiorgi M; Malaktari-Skarantavou S; Vlachopoulos C; Megremis S; Fylaktou I; Traeger-Synodinos J; Kanaka-Gantenbein C; Stefanadis C; Kanavakis E
    Hormones (Athens); 2012; 11(3):361-7. PubMed ID: 22908070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

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

  • 19. Management of Wilms tumors in Drash and Frasier syndromes.
    Auber F; Jeanpierre C; Denamur E; Jaubert F; Schleiermacher G; Patte C; Cabrol S; Leverger G; Nihoul-Fékété C; Sarnacki S
    Pediatr Blood Cancer; 2009 Jan; 52(1):55-9. PubMed ID: 18816692
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bilateral Gonadoblastoma in a 6-Year-old Girl With Frasier Syndrome: Need for Early Preventive Gonadectomy.
    Kollios K; Karipiadou A; Papagianni M; Traeger-Synodinos J; Kosta K; Savvidou P; Stabouli S; Roilides E
    J Pediatr Hematol Oncol; 2022 Nov; 44(8):471-473. PubMed ID: 35700406
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.