(Q35301762)

7 August 2017

title

Diagnostic value of fundus examination in familial adenomatous polyposis (English)

1 reference

familial adenomatous polyposis

7 August 2017

main subject

1 reference

Tiret A

1

1 reference

7 August 2017

Taiel-Sartral M

series ordinal

2

1 reference

7 August 2017

Tiret E

series ordinal

3

1 reference

7 August 2017

Laroche L

series ordinal

4

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 September 1997

1 reference

British Journal of Ophthalmology

7 August 2017

published in

1 reference

7 August 2017

volume

81

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7 August 2017

issue

9

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7 August 2017

page(s)

755-758

1 reference

A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Follow-up study of a family group exhibiting dominant inheritance for a syndrome including intestinal polyps, osteomas, fibromas and epidermal cysts.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Congenital hypertrophy of the retinal pigment epithelium as a marker for familial adenomatous polyposis.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Pigmented ocular fundus lesions in the inherited gastrointestinal polyposis syndromes and in hereditary nonpolyposis colorectal cancer.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Focal congenital anomalies of the retinal pigment epithelium.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Importance of retinal pigmentation as a subclinical marker in familial adenomatous polyposis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Pigmented lesions of the retinal pigment epithelium and familial adenomatous polyposis.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Identification of FAP locus genes from chromosome 5q21

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Familial polyposis coli: the spectrum of ocular and other extracolonic manifestations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Identification and characterization of the familial adenomatous polyposis coli gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Incidence and significance of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial adenomatous polyposis coli (FAPC)

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Retinal pigment epithelium lesions as a biomarker of disease in patients with familial adenomatous polyposis. A follow-up report

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposis.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Congenital hypertrophy of retinal pigment epithelium in non-Gardner's polyposis kindreds

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1722327

A clinicopathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner's syndrome)

26 September 2018

1 reference

12 December 2020

Hyperpigmented lesions of the retinal pigment epithelium in familial adenomatous polyposis

1 reference

12 December 2020

The Gardner syndrome. Significance of ocular features

1 reference

12 December 2020

Congenital Hypertrophy of the Retinal Pigment Epithelium

1 reference

12 December 2020

An unusual case of congenital hypertrophy of the retinal pigment epithelium

1 reference

12 December 2020

Pigmented fundus lesions in a preterm infant with familial adenomatous polyposis

1 reference

12 December 2020

Benign melanomas of the retinal pigment epithelium

1 reference

12 December 2020

Enlargement of congenital hypertrophy of the retinal pigment epithelium

1 reference

12 December 2020

Fundus changes associated with congenital hypertrophy of the retinal pigment epithelium

1 reference

12 December 2020

A histopathologic study of the pigmented fundus lesions in familial adenomatous polyposis

1 reference

12 December 2020

Histopathological features of congenital fundus lesions in familial adenomatous polyposis

1 reference

12 December 2020

Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome

1 reference

12 December 2020

Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods

1 reference

12 December 2020

Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome

1 reference

12 December 2020

Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis

1 reference

12 December 2020

Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis

1 reference

12 December 2020

Identifiers

DOI

10.1136/BJO.81.9.755

1 reference

7 August 2017

1 reference

7 August 2017

1 reference