These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

163 related items for PubMed ID: 1850823

  • 41. Ocular manifestations of familial adenomatous polyposis (Gardner syndrome).
    Traboulsi EI.
    Ophthalmol Clin North Am; 2005 Mar; 18(1):163-6, x. PubMed ID: 15763201
    [Abstract] [Full Text] [Related]

  • 42.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 43. Predictive value of congenital hypertrophy of the retinal pigment epithelium as a clinical marker for familial adenomatous polyposis.
    Heyen F, Jagelman DG, Romania A, Zakov ZN, Lavery IC, Fazio VW, McGannon E.
    Dis Colon Rectum; 1990 Dec; 33(12):1003-8. PubMed ID: 2173657
    [Abstract] [Full Text] [Related]

  • 44. Familial Adenomatous Polyposis Syndrome: An Update and Review of Extraintestinal Manifestations.
    Dinarvand P, Davaro EP, Doan JV, Ising ME, Evans NR, Phillips NJ, Lai J, Guzman MA.
    Arch Pathol Lab Med; 2019 Nov; 143(11):1382-1398. PubMed ID: 31070935
    [Abstract] [Full Text] [Related]

  • 45. [Turcot syndrome--a rare extra-intestinal manifestation of familial adenomatous polyposis?].
    Müller A, Meyenberger C, Hoppeler T, Spiegel R, Kaufmann U, Ammann R.
    Schweiz Med Wochenschr; 1993 May 29; 123(21):1125-7. PubMed ID: 8390092
    [Abstract] [Full Text] [Related]

  • 46. 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 29; 2(1):69-75. PubMed ID: 8381318
    [Abstract] [Full Text] [Related]

  • 47. Value of the congenital hypertrophy of the retinal pigment epithelium in the diagnosis of familial adenomatous polyposis.
    Touriño R, Conde-Freire R, Cabezas-Agrícola JM, Rodríguez-Aves T, López-Valladares MJ, Otero-Cepeda JL, Capeans C.
    Int Ophthalmol; 2004 Mar 29; 25(2):101-12. PubMed ID: 15290889
    [Abstract] [Full Text] [Related]

  • 48. Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis.
    Hodgson SV, Bishop DT, Jay B.
    J Med Genet; 1994 Jan 29; 31(1):55-8. PubMed ID: 8151639
    [Abstract] [Full Text] [Related]

  • 49. [Importance of the fundus oculi in the early diagnosis in childhood of familial polyposis coli].
    Díaz Llopis M, Monteagudo Montesinos E, Gutiérrez San Román C, Menezo Rozalen JL.
    Cir Pediatr; 1988 Jan 29; 1(1):39-42. PubMed ID: 2856357
    [No Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51. The Gardner syndrome. Significance of ocular features.
    Lewis RA, Crowder WE, Eierman LA, Nussbaum RL, Ferrell RE.
    Ophthalmology; 1984 Aug 29; 91(8):916-25. PubMed ID: 6493700
    [Abstract] [Full Text] [Related]

  • 52. Ganglioglioma in a patient with Turcot syndrome. Case report.
    Tamiya T, Hamazaki S, Ono Y, Tokunaga K, Matsumoto K, Furuta T, Ohmoto T.
    J Neurosurg; 2000 Jan 29; 92(1):170-5. PubMed ID: 10616098
    [Abstract] [Full Text] [Related]

  • 53. The link between colon cancer and congenital hypertrophy of the retinal pigment epithelium (CHRPE).
    Deibert B, Ferris L, Sanchez N, Weishaar P.
    Am J Ophthalmol Case Rep; 2019 Sep 29; 15():100524. PubMed ID: 31384696
    [Abstract] [Full Text] [Related]

  • 54. 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 29; 14 ( Pt 1)():18-22. PubMed ID: 10755094
    [Abstract] [Full Text] [Related]

  • 55.
    Ireland AC, Rodman J.
    ; 2024 01 29. PubMed ID: 35015449
    [Abstract] [Full Text] [Related]

  • 56. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis.
    Díaz-Llopis M, Menezo JL.
    Arch Ophthalmol; 1988 Mar 29; 106(3):412-3. PubMed ID: 2830869
    [No Abstract] [Full Text] [Related]

  • 57. 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 29; 94(5):543-8. PubMed ID: 7959691
    [Abstract] [Full Text] [Related]

  • 58. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome.
    Foulkes WD.
    QJM; 1995 Dec 29; 88(12):853-63. PubMed ID: 8593545
    [Abstract] [Full Text] [Related]

  • 59. Congenital hypertrophy of the retinal pigment epithelium associated with familial adenomatous polyposis.
    Santos A, Morales L, Hernandez-Quintela E, Jiménez-Sierra JM, Villalobos JJ, Panduro A.
    Retina; 1994 Dec 29; 14(1):6-9. PubMed ID: 8016465
    [Abstract] [Full Text] [Related]

  • 60. 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 29; 79(7):689-93. PubMed ID: 1322757
    [Abstract] [Full Text] [Related]

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