BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 38363039)

  • 1. Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins.
    Cronemberger S; Albuquerque ALB; Silva ACSE; Zanini JLSS; da Silva AHG; Barbosa LF; da Cunha Rubião F; de Lima FL; Casimiro RF; Martins MP; Diniz-Filho A; Bastos-Rodrigues L; Friedman E; De Marco L
    Acta Paediatr; 2024 Jun; 113(6):1420-1425. PubMed ID: 38363039
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case of aniridia with unilateral Peters anomaly.
    Sawada M; Sato M; Hikoya A; Wang C; Minoshima S; Azuma N; Hotta Y
    J AAPOS; 2011 Feb; 15(1):104-6. PubMed ID: 21397818
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PAX 6 is normal in most cases of Peters' anomaly.
    Churchill AJ; Booth AP; Anwar R; Markham AF
    Eye (Lond); 1998; 12 ( Pt 2)():299-303. PubMed ID: 9683959
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience.
    Hol JA; Jongmans MCJ; Sudour-Bonnange H; Ramírez-Villar GL; Chowdhury T; Rechnitzer C; Pal N; Schleiermacher G; Karow A; Kuiper RP; de Camargo B; Avcin S; Redzic D; Wachtel A; Segers H; Vujanic GM; van Tinteren H; Bergeron C; Pritchard-Jones K; Graf N; van den Heuvel-Eibrink MM;
    Cancer; 2021 Feb; 127(4):628-638. PubMed ID: 33146894
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.
    Brémond-Gignac D; Gérard-Blanluet M; Copin H; Bitoun P; Baumann C; Crolla JA; Benzacken B; Verloes A
    Am J Med Genet A; 2005 May; 134(4):422-5. PubMed ID: 15779023
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A donor twin discordant with Peters anomaly in a twin-twin transfusion syndrome case: a case report.
    Chang YL; Chao AS; Chou CY; Chang SD; Chiang MC; Lee YS
    BMC Pregnancy Childbirth; 2020 Sep; 20(1):558. PubMed ID: 32967640
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
    Dansault A; David G; Schwartz C; Jaliffa C; Vieira V; de la Houssaye G; Bigot K; Catin F; Tattu L; Chopin C; Halimi P; Roche O; Van Regemorter N; Munier F; Schorderet D; Dufier JL; Marsac C; Ricquier D; Menasche M; Penfornis A; Abitbol M
    Mol Vis; 2007 Apr; 13():511-23. PubMed ID: 17417613
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Vitreoretinal dysplasia masquerading as Peters' anomaly.
    Martinet V; Dureau P; Bergès O; Caputo G
    Eur J Ophthalmol; 2010; 20(1):228-30. PubMed ID: 19882524
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 11p13 deletion, Wilms' tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases.
    Jotterand V; Boisjoly HM; Harnois C; Bigonesse P; Laframboise R; Gagné R; St-Pierre A
    Br J Ophthalmol; 1990 Sep; 74(9):568-70. PubMed ID: 2168204
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Aniridia and Wilms tumor: 2 cases of fetal rhabdomyomatous nephroblastoma].
    Schneider P; Drouin-Garraud V; Bachy B; Brasseur G; Lahsinat K; Hemet J; Vannier JP; Tron P
    Arch Pediatr; 1996 Dec; 3(12):1243-7. PubMed ID: 9033789
    [TBL] [Abstract][Full Text] [Related]  

  • 11. WAGR syndrome--a case report.
    Mahale A; Poornima V; Shrestha M
    Nepal Med Coll J; 2007 Jun; 9(2):138-40. PubMed ID: 17899969
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Peters' anomaly and combination with other malformations (series of 16 patients).
    Mayer UM
    Ophthalmic Paediatr Genet; 1992 Jun; 13(2):131-5. PubMed ID: 1495763
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Billateral polycystic kidneys in a girl with WAGR syndrome.
    Gucev Z; Muratovska O; Laban N; Misevska L; Jancevska A; Crolla J; Tasic V
    Indian J Pediatr; 2011 Oct; 78(10):1290-2. PubMed ID: 21660403
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome.
    Marakhonov AV; Vasilyeva TA; Minzhenkova ME; Sukhanova NV; Sparber PA; Andreeva NA; Teleshova MV; Baybagisova FK; Shilova NV; Kutsev SI; Zinchenko RA
    Int J Mol Sci; 2023 Nov; 24(23):. PubMed ID: 38069245
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor.
    Lind KT; Cost NG; Zegar K; Kuldanek SA; Enzenauer RW; Schneider KW
    Ophthalmic Genet; 2021 Apr; 42(2):216-217. PubMed ID: 33300417
    [No Abstract]   [Full Text] [Related]  

  • 16. Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases.
    Wang Q; Zhang X; Qin T; Wang D; Lin X; Zhu Y; Tan H; Zhao L; Li J; Lin Z; Lin H; Chen W
    Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011342
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bilateral anterior segment dysgenesis with the presumed Peters' anomaly in a cat.
    Park S; Kim K; Kim Y; Seo K
    J Vet Med Sci; 2018 Feb; 80(2):297-301. PubMed ID: 29249729
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Peters Anomaly: Novel Non-Invasive Alternatives to Penetrating Keratoplasty.
    Rajagopal RN; Fernandes M
    Semin Ophthalmol; 2023 Apr; 38(3):275-282. PubMed ID: 36788651
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Foxe3 haploinsufficiency in mice: a model for Peters' anomaly.
    Ormestad M; Blixt A; Churchill A; Martinsson T; Enerbäck S; Carlsson P
    Invest Ophthalmol Vis Sci; 2002 May; 43(5):1350-7. PubMed ID: 11980846
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.