(Q34143920)

31 July 2017

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title

Ocular findings in a form of retinitis pigmentosa with a rhodopsin gene defect (English)

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31 July 2017

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E L Berson

1

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31 July 2017

publication date

1 January 1990

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Transactions of the American Ophthalmological Society annual meeting

31 July 2017

published in

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31 July 2017

volume

88

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31 July 2017

page(s)

355-388

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Malformation of the erythrocytes in a case of atypical retinitis pigmentosa

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

[ON THE PRESENCE OF 3,7,11,15-TETRAMETHYLHEXADECANOIC ACID (PHYTANIC ACID) IN THE CHOLESTEROL ESTERS AND OTHER LIPOID FRACTIONS OF THE ORGANS IN A CASE OF A DISEASE OF UNKNOWN ORIGIN (POSSIBLY HEREDOPATHIA ATACTICA POLYNEURITIFORMIS, REFSUM'S SYNDR

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Population genetic studies of retinitis pigmentosa.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Combined vitamin A and E therapy prevents retinal electrophysiological deterioration in abetalipoproteinaemia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Retinitis pigmentosa: clinical observations and correlations.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Isolation and nucleotide sequence of the gene encoding human rhodopsin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Rhodopsin's protein and carbohydrate structure: selected aspects.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Ocular abnormalities in abetalipoproteinemia. A clinicopathologic correlation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Cone and Rod Responses in a Family With Recessively Inherited Retinitis Pigmentosa

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Ocular histopathologic changes in a case of a-beta-lipoproteinemia (Bassen-Kornzweig syndrome)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Light deprivation for early retinitis pigmentosa. A hypothesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Pathogenesis and management of lipoprotein disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

A genetic linkage map of the human genome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Genetic regulation of light damage to photoreceptors.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Molecular genetics of inherited variation in human color vision

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Total synthesis of a gene for bovine rhodopsin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

5 July 2018

RP cone-rod degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

5 July 2018

Gene transfer into mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Molecular biology of the visual pigments

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Transgenic mice: applications to the study of the nervous system.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Tunicamycin blocks the incorporation of opsin into retinal rod outer segment membranes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Membrane morphogenesis in retinal rod outer segments: inhibition by tunicamycin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Expression of a bovine rhodopsin gene in Xenopus oocytes: demonstration of light-dependent ionic currents

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Expression of a synthetic bovine rhodopsin gene in monkey kidney cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Retinal photoreceptor-pigment epithelium interactions. Friedenwald lecture.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Molecular genetics of human blue cone monochromacy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Foveal lesions seen in retinitis pigmentosa

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Long-term management of abetalipoproteinaemia. Possible role for vitamin E

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

5 July 2018

Retinitis pigmentosa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Dominant retinitis pigmentosa with reduced penetrance. Further studies of the electroretinogram

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Visual Cell Renewal Systems and the Problem of Retinitis Pigmentosa

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

The structure of rhodopsin and its disposition in the rod outer segment disk membrane

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

The frequency of posterior subcapsular cataract in the hereditary retinal degenerations.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Dominant retinitis pigmentosa. A clinicopathologic correlation.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298597

Sex-linked retinitis pigmentosa: ultrastructure of photoreceptors and pigment epithelium

28 October 2018

1 reference

12 December 2020

Retinal ultrastructure in advanced retinitis pigmentosa

1 reference

12 December 2020

1 reference

12 December 2020

Atypical retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease

1 reference

12 December 2020

ELECTROPHYSIOLOGICAL STUDIES IN EARLY RETINITIS PIGMENTOSA

1 reference

12 December 2020

Retinitis pigmentosa. A symposium on terminology and methods of examination

1 reference

12 December 2020

Electron microscopic studies of human retinitis pigmentosa. I. Two cases of advanced retinitis pigmentosa

1 reference

12 December 2020

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

1 reference

12 December 2020

Familial electroretinographic and adaptometric studies in retinitis pigmentosa

1 reference

12 December 2020

Clinical-ultrastructural study of a retinal dystrophy

1 reference

12 December 2020

Retinitis pigmentosa in abetalipoproteinemia: Effects of vitamin A

1 reference

12 December 2020

Vitamin A and vitamin E replacement in abetalipoproteinemia

1 reference

12 December 2020

Pathology of retinitis pigmentosa

1 reference

12 December 2020

An electroretinographic and molecular genetic study of X-linked cone degeneration

1 reference

12 December 2020

No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity

1 reference

12 December 2020

Primary chorioretinal aberrations with night blindness; pathology

1 reference

12 December 2020

Assignment of the rhodopsin gene to human chromosome 3

1 reference

12 December 2020

Two forms of autosomal dominant primary retinitis pigmentosa

1 reference

12 December 2020

Potential acuity meter using a minute aerial pinhole aperture

1 reference

12 December 2020

Temporal aspects of the electroretinogram

1 reference

12 December 2020

Dominantly inherited retinitis pigmentosa. Ultrastructure and biochemical analysis

1 reference

12 December 2020

Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype

1 reference

12 December 2020

On the Protein Defect in Abetalipoproteinemia

1 reference

12 December 2020

Orientation of membrane glycoproteins in sealed rod outer segment disks

1 reference

12 December 2020

New visual acuity charts for clinical research

1 reference

12 December 2020

1 reference

12 December 2020

Prevalence of retinitis pigmentosa in Maine

1 reference

12 December 2020

Retinitis pigmentosa, the electroretinogram, and Mendel's laws

1 reference

12 December 2020

On having no beta-lipoprotein. A syndrome comprising a-beta-lipoproteinaemia, acanthocytosis, and steatorrhoea

1 reference

12 December 2020

Rod Responses in Retinitis Pigmentosa, Dominantly Inherited

1 reference

12 December 2020

Rod ERG diurnal rhythm in some patients with dominant retinitis pigmentosa

1 reference

12 December 2020

Risk Factors for Genetic Typing and Detection in Retinitis Pigmentosa

1 reference

12 December 2020

Natural course of retinitis pigmentosa over a three-year interval

1 reference

12 December 2020

Identifiers

PMC publication ID

1298597

1 reference

31 July 2017

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