(Q42965110)

11 November 2017

The electroretinogram (English)

1 reference

11 November 2017

Harden A

1

1 reference

11 November 2017

Adams GG

series ordinal

2

1 reference

11 November 2017

Taylor DS

series ordinal

3

1 reference

11 November 2017

language of work or name

English

0 references

publication date

1 July 1989

1 reference

Archives of Disease in Childhood

11 November 2017

1 reference

11 November 2017

64

1 reference

11 November 2017

7

1 reference

11 November 2017

1080-1087

1 reference

Juvenile familial nephropathy with tapetoretinal degeneration. A new oculorenal dystrophy

11 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

"Mitochondrial myopathy" or mitochondrial disease? EEG, ERG, VEP studies in 13 children

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Neurophysiological investigations in GM1 and GM2 gangliosidoses

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Non-corneal electroretinogram. Parameters in normal children

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Neurophysiological approach to disorders of vision

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Bilateral macular dysplasia ('colobomata') and congenital retinal dystrophy

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Leber's congenital amaurosis. Retrospective review of 43 cases and a new fundus finding in two cases

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Retinitis pigmentosa and deafness.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Peroxisomal disorders: a newly recognised group of genetic diseases

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

The cerebro-hepato-renal (Zellweger) syndrome and other peroxisomal disorders

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Electrophysiologic studies in neonatal adrenoleukodystrophy

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Mucolipidosis type IV: clinical spectrum and natural history.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

So-called neuronal ceroid lipofuscinosis. Neurophysiological studies in 60 children

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Neurological abnormalities in congenital amaurosis of Leber. Review of 30 cases

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Hydrocephalus, agyria, retinal dysplasia, encephalocele (HARD +/- E) syndrome: an autosomal recessive condition

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

Visual loss in osteopetrosis

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792666

[Diagnostic and prognostic importance of the electroretinogram in tapetoretinal degeneration with reduction of the visual field and hemeralopia]

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2629633

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Leber's congenital tapetoretinal degeneration

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2629633

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.64.7.1080

1 reference

11 November 2017

1 reference

11 November 2017

PubMed publication ID

2629633

1 reference