X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chrpe (17) 17
humans (16) 16
male (14) 14
female (13) 13
adult (11) 11
pigment epithelium of eye - pathology (11) 11
adenomatous polyposis coli - genetics (10) 10
familial adenomatous polyposis (9) 9
ophthalmology (9) 9
fap (8) 8
middle aged (8) 8
adolescent (7) 7
congenital hypertrophy of the retinal pigment epithelium (7) 7
hypertrophy (7) 7
adenomatous polyposis coli - pathology (6) 6
aged (6) 6
colorectal-cancer (6) 6
gardners-syndrome (6) 6
hypertrophy - congenital (6) 6
identification (6) 6
lesions (6) 6
apc gene (5) 5
child (5) 5
genes, apc (5) 5
genetics & heredity (5) 5
ocular fundus lesions (5) 5
pedigree (5) 5
phenotype (5) 5
apc mutations (4) 4
bear tracks (4) 4
child, preschool (4) 4
coli (4) 4
dna mutational analysis (4) 4
mutation (4) 4
adenomatous polyposis coli - diagnosis (3) 3
colorectal cancer (3) 3
congenital hypertrophy of retinal pigment epithelium (3) 3
desmoid tumors (3) 3
gardner syndrome (3) 3
gardner's syndrome (3) 3
gene (3) 3
genes, apc - genetics (3) 3
genotype (3) 3
hypertrophy - diagnosis (3) 3
hypertrophy - genetics (3) 3
marker (3) 3
mutations (3) 3
oncology (3) 3
retinal diseases - congenital (3) 3
sensitivity and specificity (3) 3
tumors (3) 3
adenomatous polyposis (2) 2
adenomatous polyposis coli - complications (2) 2
aged, 80 and over (2) 2
apc gen (2) 2
association (2) 2
case report (2) 2
chromosome-5q21 (2) 2
codon (2) 2
coli gene (2) 2
colon cancer (2) 2
congenital (2) 2
congenital hypertrophy (2) 2
epithelium (2) 2
familial adenomatous polyposis coli (2) 2
familiar-autosomal polyposis coli (2) 2
fundus oculi (2) 2
germ-line mutation (2) 2
halonaevus (2) 2
hypertrophy - complications (2) 2
index medicus (2) 2
locus (2) 2
ophthalmoscopy (2) 2
polymerase chain reaction (2) 2
polyposis (2) 2
predictive diagnosis (2) 2
prevalence (2) 2
retina (2) 2
retinal diseases - genetics (2) 2
retinal pigment epithelium (2) 2
retinal pigment epithelium - pathology (2) 2
retinal-pigment epithelium (2) 2
risk factors (2) 2
severity of illness index (2) 2
south africa (2) 2
subgroup (2) 2
aapc (1) 1
abnormalities (1) 1
adenoma - etiology (1) 1
adenoma - genetics (1) 1
adenomatous polyposis coli - classification (1) 1
adenomatous polyposis coli - epidemiology (1) 1
adenomatous polyposis coli - ethnology (1) 1
adenomatous polyposis coli gene (1) 1
adenomatous polyposis coli protein (1) 1
adenomatous polyposis coli protein - genetics (1) 1
adenomatous polyposis gene (1) 1
adenomatous polyposis-coli (1) 1
adenomatous polyps (1) 1
ampullary carcinoma (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


GMS ophthalmology cases, ISSN 2193-1496, 2019, Volume 9, p. Doc23
To report a case of congenital simple hamartoma of the retinal pigment epithelium (CSHRPE) with depigmentation at the margin. Case report. A 40-year-old Indian... 
CHRPE | Congenital simple hamartoma of the retinal pigment epithelium | CHRRPE | combined hamartoma of retinal and retinal pigment epithelium | CSHRPE | congenital hypertrophy of the retinal pigment epithelium
Journal Article
Saudi Journal of Ophthalmology, ISSN 1319-4534, 07/2019, Volume 33, Issue 3, pp. 260 - 267
With fewer than 100 peer-reviewed cases reported in the world to date, the underlying etiology of torpedo maculopathy has remained elusive. In this literature... 
Embryology | Nerve fiber layer | Congenital | Hypopigmentation | Distribution | Torpedo | CHRPE, congenital hypertrophy of the retinal pigment epithelium | BCVA, best corrected visual acuity | IOP, intraocular pressure | OCT, optical coherence tomography | RPE, retinal pigment epithelium
Journal Article
HPB, ISSN 1365-182X, 04/2006, Volume 8, Issue 2, pp. 155 - 156
Background. First described in 1988, attenuated familial adenomatous polyposis (AFAP) is a rare autosomal dominant precancerous condition of the... 
CHRPE | ampullary carcinoma | Attenuated familial adenomatous polyposis | Ampullary carcinoma | Case Report
Journal Article
American Journal of Ophthalmology Case Reports, ISSN 2451-9936, 09/2019, Volume 15, p. 100524
Clarify the differences between Familial Adenomatous Polyposis (FAP)-associated Congenital Hypertrophy of the Retinal Epithelium (CHRPE) and benign variants... 
Gardner syndrome | Familial adenomatous polyposis (FAP) | Colon cancer | Bear tracks | Congenital hypertrophy of the retinal epithelium (CHRPE) | Grouped pigmentation of the retina
Journal Article
Human Genetics, ISSN 0340-6717, 9/1997, Volume 100, Issue 5, pp. 601 - 605
Among 23 germline mutations identified in the APC screening of 45 familial adenomatous polyposis (FAP) patients, we have found 10 different novel frameshift... 
CHRPE | PROTEIN | FAP | LINE MUTATIONS | GENETICS & HEREDITY | IDENTIFICATION | TUMORS | LOCUS | LESIONS | K KM GENETICS & HEREDITY | Phenotype | Genes, APC - genetics | Humans | Female | Male | Aged | Adenomatous Polyposis Coli - genetics | Germ-Line Mutation - genetics | Adenomatous Polyposis Coli - pathology | Genetic Heterogeneity
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 05/1996, Volume 33, Issue 5, pp. 384 - 386
A novel mutation at codon 441 in exon 10 of the adenomatous polyposis coli (APC) gene was identified in a South African family of mixed ancestry, using a... 
Familial adenomntous polyposis coli | Frameshift mutation | Ophthalmic | Lesions (CHRPE) | familial adenomatous polyposis coli | ophthalmic lesions (CHRPE) | FAP | GENETICS & HEREDITY | CHROMOSOME-5Q21 | MUTATIONS | IDENTIFICATION | frameshift mutation | LOCUS | ADENOMATOUS POLYPOSIS
Journal Article
Journal Article
대한안과학회지, ISSN 0378-6471, 2000, Volume 41, Issue 11, pp. 2509 - 2513
선천성 망막색소상피비대증은 경계가 분명하고 편평한 색소성 망막병변으로 여러 형태로 존재하며, 선종성 용종 증후군의 하나인 가드너씨 증후군의 대장외 증상으로 흔히 나타나는 소견이다. 그 수나 형태에 따라 선종성 용종의 존재나 발달을 예측하는 지표로 중요성이 커지고 있다. 저자들은... 
Congenital hypertrophy of the retinal pigment epithelium ( CHRPE ) | Gardner`s syndrome
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.