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Results: 1 to 20 of 115

1.

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;16(12):1698-705. doi: 10.1634/theoncologist.2011-0244. Epub 2011 Dec 1.

PMID:
22135120
[PubMed - indexed for MEDLINE]
Free PMC Article
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 1;78(11):2400-10.

PMID:
8941012
[PubMed - indexed for MEDLINE]
3.

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;125(5):680-6.

PMID:
9625552
[PubMed - indexed for MEDLINE]
4.

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;5(4):397-404. Epub 2006 Aug 31.

PMID:
16944273
[PubMed - indexed for MEDLINE]
5.

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;74(4):338-42.

PMID:
8883546
[PubMed - indexed for MEDLINE]
6.

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 ( Pt 1):18-22.

PMID:
10755094
[PubMed - indexed for MEDLINE]
7.

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;111(3):278-81.

PMID:
10374435
[PubMed - indexed for MEDLINE]
Free Article
8.

Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposis.

Pang CP, Fan DS, Keung JW, Baum L, Tang NL, Lau JW, Lam DS.

Ophthalmologica. 2001 Nov-Dec;215(6):408-11.

PMID:
11741105
[PubMed - indexed for MEDLINE]
9.

Fundus lesions of adenomatous polyposis.

Tiret A, Parc C.

Curr Opin Ophthalmol. 1999 Jun;10(3):168-72. Review.

PMID:
10537774
[PubMed - indexed for MEDLINE]
10.

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;17(4):167-74.

PMID:
9010867
[PubMed - indexed for MEDLINE]
11.

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. Review.

PMID:
7714311
[PubMed - indexed for MEDLINE]
12.

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;94(5):543-8.

PMID:
7959691
[PubMed - indexed for MEDLINE]
13.

Familial adenomatous polyposis (FAP): genotype correlation to FAP phenotype with osteomas and sebaceous cysts.

Bisgaard ML, Bülow S.

Am J Med Genet A. 2006 Feb 1;140(3):200-4.

PMID:
16411234
[PubMed - indexed for MEDLINE]
14.

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;25(2):101-12.

PMID:
15290889
[PubMed - indexed for MEDLINE]
15.

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;43(5):203-9.

PMID:
9595262
[PubMed - indexed for MEDLINE]
16.

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;11 ( Pt 3):298-300.

PMID:
9373466
[PubMed - indexed for MEDLINE]
17.

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;2(1):69-75.

PMID:
8381318
[PubMed - indexed for MEDLINE]
18.

[Contribution of the ophthalmologist to presymptomatic diagnosis of familial adenomatous polyposis (FAP)].

Sommer E, Hinkel GK, Friedl W.

Ophthalmologe. 1995 Dec;92(6):809-16. German.

PMID:
8563429
[PubMed - indexed for MEDLINE]
19.

Familial adenomatous polyposis.

Half E, Bercovich D, Rozen P.

Orphanet J Rare Dis. 2009 Oct 12;4:22. doi: 10.1186/1750-1172-4-22. Review.

PMID:
19822006
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

[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;6(7):303-6. Portuguese.

PMID:
8397471
[PubMed - indexed for MEDLINE]
Free Article

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