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Journal Abstract Search

235 related items for PubMed ID: 10337595

  • 1. [Congenital hypertrophy of retinal pigment epithelium: a marker in familial adenomatous polyposis].
    Szwarcberg J, Limacher JM, Fricker JP, Flament J.
    J Fr Ophtalmol; 1999 Apr; 22(3):364-70. PubMed ID: 10337595
    [Abstract] [Full Text] [Related]

  • 2. 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; 66(2):106-12. PubMed ID: 7714311
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Assessment of the value of congenital hypertrophy of the retinal pigment epithelium as an ocular marker for familial adenomatous polyposis coli.
    Hickey-Dwyer MU, Willoughby CE.
    Eye (Lond); 1993 Dec 01; 7 ( Pt 4)():562-4. PubMed ID: 8253239
    [Abstract] [Full Text] [Related]

  • 5. 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 01; 14 ( Pt 1)():18-22. PubMed ID: 10755094
    [Abstract] [Full Text] [Related]

  • 6. Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.
    Lam DS, Kwok SP, Kwok AK, Liew CT, Lau JW, Pang CC.
    Chin Med J (Engl); 1998 Mar 01; 111(3):278-81. PubMed ID: 10374435
    [Abstract] [Full Text] [Related]

  • 7. 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 Mar 01; 11 ( Pt 3)():298-300. PubMed ID: 9373466
    [Abstract] [Full Text] [Related]

  • 8. [Value of congenital hypertrophy of the retinal pigment epithelium as diagnostic marker in familial adenomatous polyposis].
    Chagas C, Fidalgo P, Martins A, Barata A, Leitão CN, Mira FC, Ramalho PS.
    Acta Med Port; 1993 Jul 01; 6(7):303-6. PubMed ID: 8397471
    [Abstract] [Full Text] [Related]

  • 9. [Congenital hypertrophy of retinal pigment epithelium in familial colonic polyposis. Study of a family].
    Ramia Angel JM, Montero Rodríguez M, Ramírez Fe C, Sáenz Regalado D, Villeta Plaza R, Alcalde Escribano J, Morales Gutiérrez C, Abad Barahona A.
    Rev Esp Enferm Dig; 1993 Nov 01; 84(5):297-9. PubMed ID: 8305256
    [Abstract] [Full Text] [Related]

  • 10. Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods.
    Caspari R, Friedl W, Böker T, Augustin A, Mandl M, Jaeger K, Gallkowski K, Propping P.
    Z Gastroenterol; 1993 Nov 01; 31(11):646-52. PubMed ID: 8291275
    [Abstract] [Full Text] [Related]

  • 11. Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.
    Bertario L, Russo A, Sala P, Varesco L, Giarola M, Mondini P, Pierotti M, Spinelli P, Radice P, Hereditary Colorectal Tumor Registry.
    J Clin Oncol; 2003 May 01; 21(9):1698-707. PubMed ID: 12721244
    [Abstract] [Full Text] [Related]

  • 12. Ophthalmic and genetic screening in pedigrees with familial adenomatous polyposis.
    Ruhswurm I, Zehetmayer M, Dejaco C, Wolf B, Karner-Hanusch J.
    Am J Ophthalmol; 1998 May 01; 125(5):680-6. PubMed ID: 9625552
    [Abstract] [Full Text] [Related]

  • 13. Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposis.
    Morton DG, Gibson J, Macdonald F, Brown R, Haydon J, Cullen R, Rindl M, Hulten M, Neoptolemos JP, Keighley MR.
    Br J Surg; 1992 Jul 01; 79(7):689-93. PubMed ID: 1322757
    [Abstract] [Full Text] [Related]

  • 14. Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.
    Nieuwenhuis MH, Vasen HF.
    Crit Rev Oncol Hematol; 2007 Feb 01; 61(2):153-61. PubMed ID: 17064931
    [Abstract] [Full Text] [Related]

  • 15. [Possibility of presymptomatic diagnosis of familial polyposis coli].
    Renda A, Carlomagno N, Toni F, Capasso L, Peluso P, Paterno M.
    Ann Ital Chir; 1994 Feb 01; 65(3):345-9; discussion 349-50. PubMed ID: 7887588
    [Abstract] [Full Text] [Related]

  • 16. The most frequent APC mutations among Slovak familial adenomatous polyposis patients. Adenomatous polyposis coli.
    Zajac V, Kovác M, Kirchhoff T, Stevurková V, Tomka M.
    Neoplasma; 2002 Feb 01; 49(6):356-61. PubMed ID: 12584582
    [Abstract] [Full Text] [Related]

  • 17. The importance of congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis.
    Martow J, Polomeno RC, Lewandowski R, Daly D, Miller S, Jutras L, Koehn D, Der Kaloustian VM.
    Can J Ophthalmol; 1990 Oct 01; 25(6):290-2. PubMed ID: 2174290
    [Abstract] [Full Text] [Related]

  • 18. [Congenital hypertrophy of the pigment epithelium of the retina as a genetic marker in familial colonic polyposis].
    Ortiz Ortigosa S, Pineda Mariño JR, Hijos Gastón M, García-Alix Sánchez C.
    Med Clin (Barc); 1990 May 26; 94(20):797. PubMed ID: 2168009
    [No Abstract] [Full Text] [Related]

  • 19. Congenital hypertrophy of retinal pigment epithelium (CHRPE) as a marker for familial adenomatous polyposis (FAP).
    Bertario L, Bandello F, Rossetti C, Sala P, Fortini E, Spinelli P, Gennari L, Pietroiusti M, Presciuttini S.
    Eur J Cancer Prev; 1993 Jan 26; 2(1):69-75. PubMed ID: 8381318
    [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 26; 94(5):543-8. PubMed ID: 7959691
    [Abstract] [Full Text] [Related]

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