Congenital retinal dystrophies: a study of early cognitive and visual development (Q35316343)

7 August 2017

title

Congenital retinal dystrophies: a study of early cognitive and visual development (English)

1 reference

7 August 2017

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Black MM

1

1 reference

7 August 2017

Sonksen PM

series ordinal

2

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7 August 2017

language of work or name

English

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publication date

1 March 1992

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Archives of Disease in Childhood

7 August 2017

published in

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7 August 2017

volume

67

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7 August 2017

issue

3

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7 August 2017

page(s)

262-265

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Juvenile familial nephropathy with tapetoretinal degeneration. A new oculorenal dystrophy

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=1793647

Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Tapetoretinal degeneration in the cerebro-hepato-renal (Zellweger's) syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Ophthalmic manifestations of infantile phytanic acid storage disease.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Mental retardation and neurologic involvement in patients with congenital retinal blindness.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Childhood Onset Pervasive Developmental Disorder.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Characteristics of infantile autism in five children with Leber's congenital amaurosis.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Leber's congenital amaurosis--a new syndrome with a cardiomyopathy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Follow-up and diagnostic reappraisal of 75 patients with Leber's congenital amaurosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Norrie's disease: a prospective study of development

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Optic nerve hypoplasia: associations and management

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Central nervous system malformations in the CHARGE association

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Joubert syndrome. Review of the fifty-three cases so far published

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

The carbanion of nitroethane is an inhibitor of, and not a substrate for, flavocytochrome b2 [L-(+)-lactate dehydrogenase].

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Promotion of visual development of severely visually impaired babies: evaluation of a developmentally based programme.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Leber's congenital amaurosis. Is mental retardation a frequent associated defect?

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1793647

Visual development of infants with severe ocular disorders

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1374226

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Constraints upon parenting: experience of a paediatrician

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1374226

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.67.3.262

1 reference

7 August 2017

1 reference

7 August 2017

1 reference