BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 32780953)

  • 41. 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]  

  • 42. A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene.
    Okuhara K; Tajima S; Nakae J; Sasaki S; Tochimaru H; Abe S; Fujieda K
    Endocr J; 1999 Oct; 46(5):639-42. PubMed ID: 10670748
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Nephropathy gonadal dysgenesis--or incomplete Drash syndrome?].
    Schmitt K; Tulzer G; Tulzer W
    Klin Padiatr; 1992; 204(2):123-5. PubMed ID: 1583852
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. 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]  

  • 46. [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]  

  • 47. 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]  

  • 48. Gonadal tumor in Frasier syndrome: a review and classification.
    Ezaki J; Hashimoto K; Asano T; Kanda S; Akioka Y; Hattori M; Yamamoto T; Shibata N
    Cancer Prev Res (Phila); 2015 Apr; 8(4):271-6. PubMed ID: 25623218
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. 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]  

  • 51. 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]  

  • 52. 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]  

  • 53. 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]  

  • 54. Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome.
    McElreavey K; Jorgensen A; Eozenou C; Merel T; Bignon-Topalovic J; Tan DS; Houzelstein D; Buonocore F; Warr N; Kay RGG; Peycelon M; Siffroi JP; Mazen I; Achermann JC; Shcherbak Y; Leger J; Sallai A; Carel JC; Martinerie L; Le Ru R; Conway GS; Mignot B; Van Maldergem L; Bertalan R; Globa E; Brauner R; Jauch R; Nef S; Greenfield A; Bashamboo A
    Genet Med; 2020 Jan; 22(1):150-159. PubMed ID: 31337883
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromes.
    Lukusa T; Fryns JP; Kleczkowska A; Van den Berghe H
    Genet Couns; 1991; 2(1):9-16. PubMed ID: 1741980
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [XY type gonadal dysgenesis, trisomy X and variants].
    Kikuchi I; Takeuchi H; Kinoshita K
    Nihon Rinsho; 2004 Feb; 62(2):309-12. PubMed ID: 14968537
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. A novel mutation (c. 341A>G) in the SRY gene in a 46,XY female patient with gonadal dysgenesis.
    Helszer Z; Dmochowska A; Szemraj J; Słowikowska-Hilczer J; Wieczorek M; Jędrzejczyk S; Kałużewski B
    Gene; 2013 Sep; 526(2):467-70. PubMed ID: 23624391
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A Novel SRY Gene Mutation p.F109L in a 46,XY Female with Complete Gonadal Dysgenesis.
    Andonova S; Robeva R; Sirakov M; Mainhard K; Tomova A; Ledig S; Kumanov P; Savov A
    Sex Dev; 2015; 9(6):333-7. PubMed ID: 26871559
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 9.