NCL Disorders: Frequent Causes of Childhood Dementia (Q38199089)

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scientific article published on January 2013

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Language	Label	Description	Also known as
English	NCL Disorders: Frequent Causes of Childhood Dementia	scientific article published on January 2013

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scholarly article

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stated in

Europe PubMed Central

PMC publication ID

3943077

retrieved

30 August 2017

title

NCL Disorders: Frequent Causes of Childhood Dementia (English)

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stated in

Europe PubMed Central

PMC publication ID

3943077

retrieved

30 August 2017

author

Alfried Kohlschütter

series ordinal

2

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Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

author name string

Angela Schulz

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

publication date

1 January 2013

1 reference

stated in

Europe PubMed Central

PMC publication ID

3943077

retrieved

30 August 2017

published in

Iranian journal of child neurology

1 reference

stated in

Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

volume

7

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stated in

Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

issue

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

page(s)

1-8

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Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

cites work

A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.

1 reference

stated in

PubMed Central

reference URL

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6 September 2017

Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

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6 September 2017

Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

retrieved

6 September 2017

Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

retrieved

6 September 2017

Analysis of potential biomarkers and modifier genes affecting the clinical course of CLN3 disease

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

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6 September 2017

Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis

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PubMed Central

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6 September 2017

Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6

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PubMed Central

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6 September 2017

The neuronal ceroid-lipofuscinoses: from past to present

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

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6 September 2017

Kufs' disease: a critical reappraisal

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PubMed Central

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retrieved

14 September 2017

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

retrieved

14 September 2017

A rare dementing disease: adult neuronal ceroid lipofuscinoses

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

retrieved

31 August 2018

Neuronal ceroid lipofuscinoses

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943077

retrieved

1 October 2018

Identifiers

PMC publication ID

3943077

1 reference

stated in

Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

PubMed publication ID

24665282

1 reference

stated in

Europe PubMed Central

PMC publication ID

3943077

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665282%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 June 2020

 

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