199 related articles for article (PubMed ID: 9373466)
1. 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. PubMed ID: 9373466
[TBL] [Abstract][Full Text] [Related]
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; 78(11):2400-10. PubMed ID: 8941012
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 10755094
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 10374435
[TBL] [Abstract][Full Text] [Related]
5. [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
[TBL] [Abstract][Full Text] [Related]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. 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; 49(6):356-61. PubMed ID: 12584582
[TBL] [Abstract][Full Text] [Related]
8. 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; 7 ( Pt 4)():562-4. PubMed ID: 8253239
[TBL] [Abstract][Full Text] [Related]
9. [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. PubMed ID: 8397471
[TBL] [Abstract][Full Text] [Related]
10. 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; 215(6):408-11. PubMed ID: 11741105
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 9595262
[TBL] [Abstract][Full Text] [Related]
12. Exceptions to the rule: individuals with FAP specific CHRPE and mutations in exon 6 of the APC gene.
Pack K; Smith-Ravin I; Phillips RK; Hodgson SV
Clin Genet; 1996 Aug; 50(2):110-1. PubMed ID: 8937774
[No Abstract] [Full Text] [Related]
13. 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. PubMed ID: 7959691
[TBL] [Abstract][Full Text] [Related]
14. Fundus lesions of adenomatous polyposis.
Tiret A; Parc C
Curr Opin Ophthalmol; 1999 Jun; 10(3):168-72. PubMed ID: 10537774
[TBL] [Abstract][Full Text] [Related]
15. [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; 84(5):297-9. PubMed ID: 8305256
[TBL] [Abstract][Full Text] [Related]
16. The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations.
Willoughby CE
Eye (Lond); 1998; 12 ( Pt 3a)():488-9. PubMed ID: 9775260
[No Abstract] [Full Text] [Related]
17. 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. PubMed ID: 16944273
[TBL] [Abstract][Full Text] [Related]
18. Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis.
Bunyan DJ; Shea-Simonds J; Reck AC; Finnis D; Eccles DM
J Med Genet; 1995 Sep; 32(9):728-31. PubMed ID: 8544194
[TBL] [Abstract][Full Text] [Related]
19. 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; 61(2):153-61. PubMed ID: 17064931
[TBL] [Abstract][Full Text] [Related]
20. The relationship between congenital hypertrophy of the retinal pigment epithelium (CHRPE) and germline mutations in the adenomatous polyposis coli (APC) gene.
Ziskind A; Kitze MJ; Grobbelaar JJ
Ophthalmic Genet; 1999 Mar; 20(1):53-6. PubMed ID: 10454823
[No Abstract] [Full Text] [Related]
[Next] [New Search]