(Q35762479)

10 August 2017

0 references

Batten disease: features to facilitate early diagnosis (English)

1 reference

10 August 2017

J Collins

1

1 reference

10 August 2017

G E Holder

series ordinal

2

1 reference

10 August 2017

H Herbert

series ordinal

3

1 reference

10 August 2017

G G W Adams

series ordinal

4

1 reference

10 August 2017

language of work or name

English

0 references

publication date

5 June 2006

1 reference

British Journal of Ophthalmology

10 August 2017

1 reference

10 August 2017

90

1 reference

10 August 2017

9

1 reference

10 August 2017

1119-1124

1 reference

The intracellular location and function of proteins of neuronal ceroid lipofuscinoses

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

The genetic spectrum of human neuronal ceroid-lipofuscinoses

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Current state of clinical and morphological features in human NCL.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Isolation of a novel gene underlying Batten disease, CLN3. The International Batten Disease Consortium

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Juvenile Batten's disease: an ophthalmological assessment of 26 patients

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Electroretinographic and clinicopathologic correlations of retinal dysfunction in infantile neuronal ceroid lipofuscinosis (infantile Batten disease).

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Neuronal ceroid lipofuscinosis: a clinicopathological study.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Evaluation of the electrodiagnostic investigation of children using the Greenwich Grading System

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

Duane's retraction syndrome and juvenile Batten's disease: a new association?

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857407

The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses

25 September 2018

1 reference

12 December 2020

Batten disease--deteriorating course of ocular findings

1 reference

12 December 2020

Refsum disease: The presentation and ophthalmic aspects of Refsum disease in a series of 23 patients

1 reference

12 December 2020

Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene

1 reference

12 December 2020

Identifiers

DOI

10.1136/BJO.2006.091637

1 reference

10 August 2017

1 reference

10 August 2017

1 reference