BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 9593608)

  • 1. XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome.
    Murray SC
    J Pediatr Adolesc Gynecol; 1998 May; 11(2):89-91. PubMed ID: 9593608
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A syndrome of chronic renal failure and XY gonadal dysgenesis in young phenotypic females without genital ambiguity.
    Haning RV; Chesney RW; Moorthy AV; Gilbert EF
    Am J Kidney Dis; 1985 Jul; 6(1):40-8. PubMed ID: 3895900
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases.
    Moorthy AV; Chesney RW; Lubinsky M
    Am J Med Genet Suppl; 1987; 3():297-302. PubMed ID: 3130865
    [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. Nephropathy-gonadal dysgenesis, type 2: renal failure in three siblings with XY dysgenesis in one.
    Kinberg JA; Angle CR; Wilson RB
    Am J Kidney Dis; 1987 Jun; 9(6):507-10. PubMed ID: 3591796
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Familial 46,XX gonadal dysgenesis.
    Aleem FA
    Fertil Steril; 1981 Mar; 35(3):317-20. PubMed ID: 7202756
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Renal failure wit XY gonadal dysgenesis: report of the second case.
    Harkins PG; Haning RV; Shapiro SS
    Obstet Gynecol; 1980 Dec; 56(6):751-2. PubMed ID: 7443120
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Bilateral ovariectomy in gonadal dysgenesis with a Y chromosome].
    Za G; Figini E; Passamonti U; Lituania M; Cordone M; Bocchino G; Esposito V; Grimaldi M; Savioli C; Morando A
    Minerva Ginecol; 1992; 44(1-2):55-61. PubMed ID: 1508386
    [TBL] [Abstract][Full Text] [Related]  

  • 10. End-stage renal disease and primary hypogonadism associated with a 46,XX karyotype.
    Bailey WA; Zwingman TA; Reznik VM; Griswold WR; Mendoza SA; Jones KL; Freidenberg GR
    Am J Dis Child; 1992 Oct; 146(10):1218-23. PubMed ID: 1329488
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Absent pubertal development in a child with chronic renal failure: the case of Frasier syndrome.
    Bönte A; Schröder W; Denamur E; Querfeld U
    Nephrol Dial Transplant; 2000 Oct; 15(10):1688-90. PubMed ID: 11007843
    [No Abstract]   [Full Text] [Related]  

  • 12. Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis.
    Keskin M; Savaş-Erdeve Ş; Kurnaz E; Çetinkaya S; Karaman A; Apaydın S; Aycan Z
    Turk J Pediatr; 2016; 58(5):538-540. PubMed ID: 28621097
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Management of phenotypic female patients with an XY karyotype.
    Portuondo JA; Neyro JL; Barral A; Gonzalez-Gorospe F; Benito JA
    J Reprod Med; 1986 Jul; 31(7):611-5. PubMed ID: 3091820
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial 46,XY pure gonadal dysgenesis and gonadoblastoma/dysgerminoma: case report.
    Berg FD; Kürzl R; Hinrichsen MJ; Zander J
    Gynecol Oncol; 1989 Feb; 32(2):261-7. PubMed ID: 2910791
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Diagnostic principles of gonadal dysgenesis in adolescents].
    Chipashvili MK; Kristesashvili DI; Chopikashvili NA; Kopaliani NSh
    Georgian Med News; 2005 Nov; (128):24-8. PubMed ID: 16369057
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical heterogeneity in children with gonadal dysgenesis associated with non-mosaic 46,XY karyotype.
    Wong YS; Tam YH; Pang KKY; To KF; Chan SSC; Chan KW; Lee KH
    J Pediatr Urol; 2017 Oct; 13(5):508.e1-508.e6. PubMed ID: 28434637
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosomal complements in primary gonadal failure.
    Portuondo JA; Barral A; Melchor JC; Tanago JG; Neyro JL
    Obstet Gynecol; 1984 Dec; 64(6):757-61. PubMed ID: 6504419
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Complete development of secondary sex characteristics in a case of 46,XY pure gonadal dysgenesis.
    Villanueva AL; Benirschke K; Campbell J; Wachtel SS; Rebar RW
    Obstet Gynecol; 1984 Sep; 64(3 Suppl):68S-72S. PubMed ID: 6433251
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic heterogeneity of XY gonadal dysgenesis (Swyer syndrome): H-Y antigen-negative XY gonadal dysgenesis associated with inflammatory bowel disease.
    Passarge E; Wolf U
    Am J Med Genet; 1981; 8(4):437-41. PubMed ID: 7246614
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature Review.
    Lavi E; Zighan M; Abu Libdeh A; Klopstock T; Weinberg-Shukron A; Renbaum P; Levy-Lahad E; Zangen D
    Pediatr Endocrinol Rev; 2020 Aug; 17(4):302-307. PubMed ID: 32780953
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.