BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

322 related articles for article (PubMed ID: 19653292)

  • 1. 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]  

  • 2. 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]  

  • 3. A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.
    Hersmus R; van der Zwan YG; Stoop H; Bernard P; Sreenivasan R; Oosterhuis JW; Brüggenwirth HT; de Boer S; White S; Wolffenbuttel KP; Alders M; McElreavy K; Drop SL; Harley VR; Looijenga LH
    PLoS One; 2012; 7(7):e40858. PubMed ID: 22815844
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Tumors of dysgenetic gonads in Swyer syndrome.
    Zieliñska D; Zajaczek S; Rzepka-Górska I
    J Pediatr Surg; 2007 Oct; 42(10):1721-4. PubMed ID: 17923202
    [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. 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]  

  • 8. Gonadoblastoma with contralateral dysgerminoma in a young female--a case report.
    Jadhav MN; Yelikar BR; Karigoudar M
    Indian J Pathol Microbiol; 2006 Apr; 49(2):274-6. PubMed ID: 16933739
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. [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]  

  • 12. Characteristics of testicular dysgenesis syndrome and decreased expression of SRY and SOX9 in Frasier syndrome.
    Schumacher V; Gueler B; Looijenga LH; Becker JU; Amann K; Engers R; Dotsch J; Stoop H; Schulz W; Royer-Pokora B
    Mol Reprod Dev; 2008 Sep; 75(9):1484-94. PubMed ID: 18271004
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Coexistence of a choriocarcinoma and a gonadoblastoma in the gonad of a 46,XY female: a single nucleotide polymorphism array analysis.
    Beaulieu Bergeron M; Soglio DB; Maietta A; Fournet JC; Blumenkrantz M; Brochu P; Lemieux N
    Pediatr Dev Pathol; 2010; 13(1):66-71. PubMed ID: 19425818
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bilateral ovarian gonadoblastoma with coexisting dysgerminoma in a girl with 46, XX karyotype.
    Yilmaz B; Gungor T; Bayramoglu H; Soysal S; Mollamahmutoglu L
    J Obstet Gynaecol Res; 2010 Jun; 36(3):697-700. PubMed ID: 20598061
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bilateral gonadoblastomas with a left sided dysgerminoma in a true hermaphrodite (disorder of sexual differentiation) with 46, XY karyotype.
    Kini U; Bantwal G; Ayyar V; Idiculla J
    J Assoc Physicians India; 2008 Jul; 56():549-51. PubMed ID: 18846912
    [TBL] [Abstract][Full Text] [Related]  

  • 18. WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case report.
    Finken MJ; Hendriks YM; van der Voorn JP; Veening MA; Lombardi MP; Rotteveel J
    Horm Res Paediatr; 2015; 83(3):211-6. PubMed ID: 25613702
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frasier syndrome comes full circle: genetic studies performed in an original patient.
    Wang NJ; Song HR; Schanen NC; Litman NL; Frasier SD
    J Pediatr; 2005 Jun; 146(6):843-4. PubMed ID: 15973330
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recurrence of a dysgerminoma in Frasier syndrome.
    Mestrallet G; Bertholet-Thomas A; Ranchin B; Bouvier R; Frappaz D; Cochat P
    Pediatr Transplant; 2011 May; 15(3):e53-5. PubMed ID: 20408995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.