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Items: 1 to 20 of 99

1.

The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.

Burn J, Chapman P, Delhanty J, Wood C, Lalloo F, Cachon-Gonzalez MB, Tsioupra K, Church W, Rhodes M, Gunn A.

J Med Genet. 1991 May;28(5):289-96.

2.

Congenital hypertrophy of the retinal pigment epithelium predicts colorectal polyposis in Gardner's syndrome.

Traboulsi EI, Maumenee IH, Krush AJ, Alcorn D, Giardiello FM, Burt RW, Hughes JP, Hamilton SR.

Arch Ophthalmol. 1990 Apr;108(4):525-6.

PMID:
2157384
3.
4.

Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposis.

Chapman PD, Church W, Burn J, Gunn A.

BMJ. 1989 Feb 11;298(6670):353-4.

5.

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
6.

Lack of association among typical congenital hypertrophy of the retinal pigment epithelium, adenomatous polyposis, and Gardner syndrome.

Shields JA, Shields CL, Shah PG, Pastore DJ, Imperiale SM Jr.

Ophthalmology. 1992 Nov;99(11):1709-13.

PMID:
1333580
7.

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.

8.

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, et al.

Br J Surg. 1992 Jul;79(7):689-93.

PMID:
1322757
9.

[When is congenital hypertrophy of the retinal pigment epithelium (CHRPE) associated with the Gardner's syndrome? An overview with clinical examples].

Meyer CH, Becker R, Schmidt JC, Kroll P.

Klin Monbl Augenheilkd. 2002 Sep;219(9):644-8. German.

PMID:
12410463
10.

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. doi: 10.1186/1756-0500-7-734.

11.

Familial variation in retinal pigmentation in adenomatous polyposis.

Parker JA, Berk T, Bapat BV.

Can J Ophthalmol. 1995 Apr;30(3):138-41.

PMID:
7627898
13.

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
14.

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
15.

Association of congenital hypertrophy of the retinal pigment epithelium with familial adenomatous polyposis.

Iwama T, Mishima Y, Okamoto N, Inoue J.

Br J Surg. 1990 Mar;77(3):273-6.

PMID:
2157519
16.

[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.

17.

[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. French.

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
19.
20.

[Presymptomatic detection of familial colonic polyposis].

Ducroix JP, Lenaerts C, Milazzo S, Dupas JL, Olschwang S, Lafont B, Smail A, Baillet J, Puissan C.

Rev Med Interne. 1993;14(10):983. French.

PMID:
8009076

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