BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 37074092)

  • 1. Seminoma in 46, XY Gonadal Dysgenesis: Rare Presentation and Review of the Literature.
    Adra M; Nakanishi H; Papachristodoulou E; Karaoli E; Gerasimou P; Miltiadous A; Nicolaou K; Loizou L; Skordis N
    J Clin Res Pediatr Endocrinol; 2023 Apr; ():. PubMed ID: 37074092
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A Risk of Gonadoblastoma in Familial Swyer Syndrome-A Case Report and Literature Review.
    Rudnicka E; Jaroń A; Kruszewska J; Smolarczyk R; Jażdżewski K; Derlatka P; Kucharska AM
    J Clin Med; 2024 Jan; 13(3):. PubMed ID: 38337479
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gonadoblastoma Y locus genes expressed in germ cells of individuals with dysgenetic gonads and a Y chromosome in their karyotypes include DDX3Y and TSPY.
    Vogt PH; Besikoglu B; Bettendorf M; Frank-Herrmann P; Zimmer J; Bender U; Knauer-Fischer S; Choukair D; Sinn P; Lau YC; Heidemann PH; Strowitzki T
    Hum Reprod; 2019 Apr; 34(4):770-779. PubMed ID: 30753444
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 46, XY complete gonadal dysgenesis with pubertal virilisation due to dysgerminoma/gonadoblastoma.
    Alam S; Boro H; Goyal A; Khadgawat R
    BMJ Case Rep; 2020 Jul; 13(7):. PubMed ID: 32641439
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Swyer syndrome in a woman with pure 46,XY gonadal dysgenesis: a rare presentation.
    Maharjan A; Yao-Dan L; Li H
    Clin Exp Obstet Gynecol; 2017; 44(2):314-316. PubMed ID: 29746049
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel mutation of MAP3K1 gene in 46,XY DSD with complete gonadal dysgenesis.
    Yu PH; Tsai MC; Chiang CT; Wang HY; Kuo PL
    Taiwan J Obstet Gynecol; 2022 Sep; 61(5):903-905. PubMed ID: 36088066
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A rare case of primary amenorrhoea and breast development in a 46,XY 15-year-old girl.
    Morawiecka-Pietrzak M; Dąbrowska E; Gliwińska A; Góra A; Geisler G; Gawlik A; Kudela G; Ziora K
    Pediatr Endocrinol Diabetes Metab; 2021; 27(1):62-67. PubMed ID: 33599439
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Swyer Syndrome: A Case of Dysgerminoma Solely within the Fallopian Tube.
    Anwar A; Akhtar M; Busby G
    J Pediatr Adolesc Gynecol; 2021 Dec; 34(6):869-871. PubMed ID: 33989803
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation.
    Çatlı G; Alparslan C; Can PŞ; Akbay S; Kelekçi S; Atik T; Özyılmaz B; Dündar BN
    J Clin Res Pediatr Endocrinol; 2015 Jun; 7(2):159-62. PubMed ID: 26316442
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Coexistence of gonadoblastoma and dysgerminoma in a dysgenetic gonad on touch preparation: a case report.
    Maleki Z; Loveless M; Fraig M
    Diagn Cytopathol; 2011 Jan; 39(1):42-4. PubMed ID: 21162092
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report.
    Mutlu GY; Kırmızıbekmez H; Aydın H; Çetiner H; Moralıoğlu S; Celayir AC
    J Pediatr Endocrinol Metab; 2015 Jan; 28(1-2):207-10. PubMed ID: 25153220
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Imaging Findings in Dysgerminoma in a Case of 46 XY, Complete Gonadal Dysgenesis (Swyer syndrome).
    Yadav P; Khaladkar S; Gujrati A
    J Clin Diagn Res; 2016 Sep; 10(9):TD10-TD12. PubMed ID: 27790550
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. EARLY-ONSET GONADOBLASTOMA IN A 13-MONTH-OLD INFANT WITH 46,XY COMPLETE GONADAL DYSGENESIS IDENTIFIED WITH PRENATAL TESTING: A CASE OF CHROMOSOME 9p DELETION.
    Fredette ME; Cusmano K; Phornphutkul C; Schwab J; Caldamone A; Topor LS
    AACE Clin Case Rep; 2019; 5(6):e380-e383. PubMed ID: 31967076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dysgerminoma in a case of 46, XY pure gonadal dysgenesis (Swyer syndrome): a case report.
    Han Y; Wang Y; Li Q; Dai S; He A; Wang E
    Diagn Pathol; 2011 Sep; 6():84. PubMed ID: 21929773
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Gonadal dysgenesis and gynecologic cancer.
    Jonson AL; Geller MA; Dickson EL
    Obstet Gynecol; 2010 Aug; 116 Suppl 2():550-552. PubMed ID: 20664451
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Pure 46,XY gonadal dysgenesis].
    Ságodi L; Ladányi E; Kiss Á; Tar A; Lukács V; Minik K; Vámosi I
    Orv Hetil; 2010 Nov; 151(48):1991-5. PubMed ID: 21084251
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.