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

213 related items for PubMed ID: 7571988

  • 1. The clinical [corrected] background of familial adenomatous polyposis. History, epidemiology, diagnosis and treatment.
    Kartheuser A, Detry R, West S, Coppens JP, Gribomont AC, Hoang P, Melange M, Vanheuverzwyn R, Verellen-Dumoulin C, Burn J.
    Acta Gastroenterol Belg; 1995; 58(2):252-66. PubMed ID: 7571988
    [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. 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]

  • 4. 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]

  • 5. 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]

  • 6. 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 01; 5(4):397-404. PubMed ID: 16944273
    [Abstract] [Full Text] [Related]

  • 7.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Yen T, Stanich PP, Axell L, Patel SG.
    ; 1993 Nov 01. PubMed ID: 20301519
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.
    Caspari R, Olschwang S, Friedl W, Mandl M, Boisson C, Böker T, Augustin A, Kadmon M, Möslein G, Thomas G.
    Hum Mol Genet; 1995 Mar 01; 4(3):337-40. PubMed ID: 7795585
    [Abstract] [Full Text] [Related]

  • 11. Congenital hypertrophy of the retinal pigment epithelium as a marker for familial adenomatous polyposis.
    Berk T, Cohen Z, McLeod RS, Parker JA.
    Dis Colon Rectum; 1988 Apr 01; 31(4):253-7. PubMed ID: 2896112
    [Abstract] [Full Text] [Related]

  • 12. [Familial adenomatous polyposis: what is new for the clinician?].
    Coppens JP, Kartheuser A, Verellen-Dumoulin C, Gribomont AC, Detry R, Van Heuverzwyn R.
    Acta Gastroenterol Belg; 1992 Apr 01; 55(5-6):457-61. PubMed ID: 1337641
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Desmoid Tumors in Familial Adenomatous Polyposis.
    DE Marchis ML, Tonelli F, Quaresmini D, Lovero D, Della-Morte D, Silvestris F, Guadagni F, Palmirotta R.
    Anticancer Res; 2017 Jul 01; 37(7):3357-3366. PubMed ID: 28668823
    [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 Jul 01; 11 ( Pt 3)():298-300. PubMed ID: 9373466
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Desmoid tumour biology in patients with familial adenomatous polyposis coli.
    Schiessling S, Kihm M, Ganschow P, Kadmon G, Büchler MW, Kadmon M.
    Br J Surg; 2013 Apr 01; 100(5):694-703. PubMed ID: 23334997
    [Abstract] [Full Text] [Related]

  • 18. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP).
    Rossato M, Rigotti M, Grazia M, Turco AE, Bonomi L.
    Acta Ophthalmol Scand; 1996 Aug 01; 74(4):338-42. PubMed ID: 8883546
    [Abstract] [Full Text] [Related]

  • 19. Familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC): a review of clinical, genetic and therapeutic aspects.
    Soravia C, Bapat B, Cohen Z.
    Schweiz Med Wochenschr; 1997 Apr 19; 127(16):682-90. PubMed ID: 9140167
    [Abstract] [Full Text] [Related]

  • 20. Identification of APC exon 15 mutations in families suspected of familial adenomatous polyposis (FAP).
    Kirchhoff T, Zajac V, Krizan P, Repiská V, Stevurková V, Friedl W.
    Folia Biol (Praha); 1997 Apr 19; 43(5):203-9. PubMed ID: 9595262
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.