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140 related items for PubMed ID: 33148946

  • 1. RETINAL PIGMENT EPITHELIAL LESIONS ASSOCIATED WITH A SPORADIC CASE OF FAMILIAL ADENOMATOUS POLYPOSIS.
    Alsberge JB, Peng MY, Agarwal A, McDonald HR.
    Retin Cases Brief Rep; 2022 Nov 01; 16(6):759-761. PubMed ID: 33148946
    [Abstract] [Full Text] [Related]

  • 2. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations.
    Valanzano R, Cama A, Volpe R, Curia MC, Mencucci R, Palmirotta R, Battista P, Ficari F, Mariani-Costantini R, Tonelli F.
    Cancer; 1996 Dec 01; 78(11):2400-10. PubMed ID: 8941012
    [Abstract] [Full Text] [Related]

  • 3. Study of diagnostic value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.
    Cai S, Yu Y, Xie X, Huang Y, Song Y, Zhan S, Zheng S.
    Eur J Cancer Prev; 2022 Sep 01; 31(5):422-429. PubMed ID: 35191403
    [Abstract] [Full Text] [Related]

  • 4. Congenital hypertrophy of the retinal pigment epithelium serves as a clinical marker in a family with familial adenomatous polyposis.
    Parisi ML.
    J Am Optom Assoc; 1995 Feb 01; 66(2):106-12. PubMed ID: 7714311
    [Abstract] [Full Text] [Related]

  • 5. Familial adenomatous polyposis.
    Half E, Bercovich D, Rozen P.
    Orphanet J Rare Dis; 2009 Oct 12; 4():22. PubMed ID: 19822006
    [Abstract] [Full Text] [Related]

  • 6. Congenital hypertrophy of retinal pigment epithelium (CHRPE) in patients with familial adenomatous polyposis (FAP); a polyposis registry experience.
    Nusliha A, Dalpatadu U, Amarasinghe B, Chandrasinghe PC, Deen KI.
    BMC Res Notes; 2014 Oct 18; 7():734. PubMed ID: 25326340
    [Abstract] [Full Text] [Related]

  • 7. Optical coherence tomography findings of pigmented fundus lesions in familial adenomatous polyposis.
    Tzu JH, Cavuoto KM, Villegas VM, Dubovy SR, Capo H.
    Ophthalmic Surg Lasers Imaging Retina; 2014 Oct 18; 45(1):69-70. PubMed ID: 24266367
    [Abstract] [Full Text] [Related]

  • 8. Atypical hypertrophy of retinal pigment epithelium manifesting as the first sign of familial adenomatous polyposis.
    Ponces Ramalhão J, Afonso M, Macedo M, Araújo M.
    BMJ Case Rep; 2023 Nov 14; 16(11):. PubMed ID: 37963665
    [Abstract] [Full Text] [Related]

  • 9. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer.
    Chen CS, Phillips KD, Grist S, Bennet G, Craig JE, Muecke JS, Suthers GK.
    Fam Cancer; 2006 Nov 14; 5(4):397-404. PubMed ID: 16944273
    [Abstract] [Full Text] [Related]

  • 10. A Patient With Desmoid Tumors and Familial FAP Having Frame Shift Mutation of the APC Gene.
    Sadighi S, Ghaffari-Moghaddam M, Saffari M, Mohagheghi MA, Shirkoohi R.
    Acta Med Iran; 2017 Feb 14; 55(2):134-138. PubMed ID: 28282712
    [Abstract] [Full Text] [Related]

  • 11. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in two Chinese families with familial adenomatous polyposis.
    Pang CP, Keung JW, Tang NL, Fan DS, Lau JW, Lam DS.
    Eye (Lond); 2000 Feb 14; 14 ( Pt 1)():18-22. PubMed ID: 10755094
    [Abstract] [Full Text] [Related]

  • 12. The natural history of familial adenomatous polyposis syndrome: a 24 year review of a single center experience in screening, diagnosis, and outcomes.
    Kennedy RD, Potter DD, Moir CR, El-Youssef M.
    J Pediatr Surg; 2014 Jan 14; 49(1):82-6. PubMed ID: 24439586
    [Abstract] [Full Text] [Related]

  • 13. Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?
    Burger B, Cattani N, Trueb S, de Lorenzo R, Albertini M, Bontognali E, Itin C, Schaub N, Itin PH, Heinimann K.
    Oncologist; 2011 Jan 14; 16(12):1698-705. PubMed ID: 22135120
    [Abstract] [Full Text] [Related]

  • 14. Pigmented Ocular Fundus Lesions Associated With Familial Adenomatous Polyposis.
    Li CJ, Yaghy A, Shields CL.
    Ophthalmic Surg Lasers Imaging Retina; 2020 Feb 01; 51(2):124. PubMed ID: 32084287
    [Abstract] [Full Text] [Related]

  • 15. The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations.
    Reck AC, Bunyan D, Eccles D, Humphry R.
    Eye (Lond); 1997 Feb 01; 11 ( Pt 3)():298-300. PubMed ID: 9373466
    [Abstract] [Full Text] [Related]

  • 16. Pigmented ocular fundus lesions and APC mutations in familial adenomatous polyposis.
    Traboulsi EI, Apostolides J, Giardiello FM, Krush AJ, Booker SV, Hamilton SR, Hussels IE.
    Ophthalmic Genet; 1996 Dec 01; 17(4):167-74. PubMed ID: 9010867
    [Abstract] [Full Text] [Related]

  • 17. Fundic gland polyps in familial adenomatous polyposis: neoplasms with frequent somatic adenomatous polyposis coli gene alterations.
    Abraham SC, Nobukawa B, Giardiello FM, Hamilton SR, Wu TT.
    Am J Pathol; 2000 Sep 01; 157(3):747-54. PubMed ID: 10980114
    [Abstract] [Full Text] [Related]

  • 18. Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report.
    Khider F, Cherbal F, Boumehdi AL, Layaida K, Mahfouf H, Zebboudj F, Maaoui M.
    Mol Biol Rep; 2022 May 01; 49(5):3823-3837. PubMed ID: 35142982
    [Abstract] [Full Text] [Related]

  • 19. Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP).
    Bapat B, Berk T, Mitri A, Cohen Z, Gallinger S, Stern H.
    Hum Mutat; 1994 May 01; 4(4):253-6. PubMed ID: 7866403
    [Abstract] [Full Text] [Related]

  • 20. Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis.
    Wallis YL, Macdonald F, Hultén M, Morton JE, McKeown CM, Neoptolemos JP, Keighley M, Morton DG.
    Hum Genet; 1994 Nov 01; 94(5):543-8. PubMed ID: 7959691
    [Abstract] [Full Text] [Related]

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