(Q37708247)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24719134%20AND%20SRC:MED&resulttype=core&format=json

13 March 2020

title

Clinical and genetic aspects in twelve Korean patients with adrenomyeloneuropathy (English)

1 reference

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13 March 2020

2

1 reference

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13 March 2020

Phil Hyu Lee

8

1 reference

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13 March 2020

3

Hoon-Chul Kang

1 reference

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13 March 2020

author name string

Hyung Jun Park

1

1 reference

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13 March 2020

Byung-Ok Choi

4

1 reference

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13 March 2020

Bum Chun Suh

5

1 reference

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13 March 2020

Ho Jin Kim

6

1 reference

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13 March 2020

Young-Chul Choi

7

1 reference

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13 March 2020

Seung Min Kim

9

1 reference

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13 March 2020

publication date

1 April 2014

1 reference

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13 March 2020

published in

Yonsei Medical Journal

1 reference

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13 March 2020

volume

55

1 reference

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13 March 2020

issue

3

1 reference

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13 March 2020

page(s)

676-682

1 reference

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Creative Commons Attribution-NonCommercial 3.0 Unported

13 March 2020

copyright license

start time

1 January 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Peroxisomal leukoencephalopathy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

X-linked adrenoleukodystrophy.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Adrenomyeloneuropathy: a neuropathologic review featuring its noninflammatory myelopathy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Nerve conduction studies in adrenomyeloneuropathy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Mutational analysis of patients with X-linked adrenoleukodystrophy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Familial spinocerebellar degeneration as an expression of adrenoleukodystrophy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Phenotypic variability in a family with x-linked adrenoleukodystrophy caused by the p.Trp132Ter mutation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

The genetically modified polysialylated form of neural cell adhesion molecule-positive cells for potential treatment of X-linked adrenoleukodystrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

MRI of adrenoleukodystrophy involving predominantly the cerebellum and brain stem

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Efferent and afferent evoked potentials in patients with adrenomyeloneuropathy

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

X-linked adrenoleukodystrophy: spinocerebellar variant

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Dentato-rubral tract involvement in adult-onset adrenoleukodystrophy.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Abnormalities of somatosensory and motor evoked potentials in adrenomyeloneuropathy: comparison with magnetic resonance imaging and clinical findings.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Adrenoleukodystrophy: a clinical variant presenting as olivopontocerebellar atrophy

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990087

Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene

1 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24719134

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Epidemiology of X-linked adrenoleukodystrophy in Japan

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24719134

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Phenotypic heterogeneity of an adult form of adrenoleukodystrophy in monozygotic twins

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24719134

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3349/YMJ.2014.55.3.676

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24719134%20AND%20SRC:MED&resulttype=core&format=json

13 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24719134%20AND%20SRC:MED&resulttype=core&format=json

13 March 2020

PubMed publication ID

24719134

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24719134%20AND%20SRC:MED&resulttype=core&format=json