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Wilson's disease and other neurological copper disorders
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scholarly article
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stated in
Europe PubMed Central
PubMed publication ID
25496901
retrieved
6 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Wilson's disease and other neurological copper disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25496901
retrieved
6 August 2017
main subject
copper
0 references
author
Oliver Bandmann
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
author name string
Karl Heinz Weiss
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
Stephen G Kaler
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
publication date
1 January 2015
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25496901
retrieved
6 August 2017
published in
Lancet Neurology
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
volume
14
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
issue
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
page(s)
103-113
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
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Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin
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Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy
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Evolving perspectives in Wilson disease: diagnosis, treatment and monitoring
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ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model
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Rescue of ATP7B function in hepatocyte-like cells from Wilson's disease induced pluripotent stem cells using gene therapy or the chaperone drug curcumin
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Liver mitochondrial membrane crosslinking and destruction in a rat model of Wilson disease
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Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease
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Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy
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Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease.
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9 July 2018
Treatment of Wilson's disease with tetrathiomolybdate: V. Control of free copper by tetrathiomolybdate and a comparison with trientine
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Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord
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9 July 2018
Atp7b-/- mice as a model for studies of Wilson's disease
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High incidence and allelic homogeneity of Wilson disease in 2 isolated populations: a prerequisite for efficient disease prevention programs
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The neurological presentation of ceruloplasmin gene mutations
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Neonatal diagnosis and treatment of Menkes disease
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The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration
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Ocular motility and Wilson's disease: a study on 34 patients
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9 July 2018
Liver cell death and anemia in Wilson disease involve acid sphingomyelinase and ceramide
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9 July 2018
Neurological manifestations in Wilson's disease: Report of 119 cases
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9 July 2018
Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing
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9 July 2018
Pilot study of screening for Wilson disease using dried blood spots obtained from children seen at outpatient clinics
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9 July 2018
Treatment of Wilson's disease with zinc: XV long-term follow-up studies
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9 July 2018
Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses
1 reference
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9 July 2018
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
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=4336199
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9 July 2018
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.
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9 July 2018
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
1 reference
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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=4336199
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9 July 2018
Wilson's disease and epilepsy
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PubMed Central
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9 July 2018
Dangers of non-compliance in Wilson's disease
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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=4336199
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9 July 2018
Alterations in the levels of iron, ferritin and other trace metals in Parkinson's disease and other neurodegenerative diseases affecting the basal ganglia
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9 July 2018
Wilson's disease in Scotland
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9 July 2018
Decrease of D2 receptors indicated by 123I-iodobenzamide single-photon emission computed tomography relates to neurological deficit in treated Wilson's disease
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9 July 2018
Does brain degeneration in Wilson disease involve not only copper but also iron accumulation?
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27 September 2018
Compliant treatment with anti-copper agents prevents clinically overt Wilson's disease in pre-symptomatic patients
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27 September 2018
Seven-tesla magnetic resonance imaging in Wilson disease using quantitative susceptibility mapping for measurement of copper accumulation
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27 September 2018
Extensive striatal, cortical, and white matter brain MRI abnormalities in Wilson disease
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27 September 2018
Samuel Alexander Kinnier Wilson. Wilson's disease, Queen Square and neurology
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27 September 2018
Cognitive profile in Wilson's disease: a case series of 31 patients
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27 September 2018
Outcome and development of symptoms after orthotopic liver transplantation for Wilson disease.
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27 September 2018
Never forget aceruloplasminemia in case of highly suggestive Wilson's disease score
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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=4336199
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27 September 2018
Spasmodic muscle cramps and weakness as presenting symptoms in Wilson disease
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27 September 2018
Effect of liver transplantation on brain magnetic resonance imaging pathology in Wilson disease: a case report
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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=4336199
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27 September 2018
Copper enhances APP dimerization and promotes Aβ production
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27 September 2018
Wilson disease in offspring of affected patients: report of four French families
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27 September 2018
Efficacy and safety of oral chelators in treatment of patients with Wilson disease.
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PubMed Central
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27 September 2018
Ceruloplasmin dysfunction and therapeutic potential for Parkinson disease.
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PubMed Central
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27 September 2018
Early gestational gene transfer with targeted ATP7B expression in the liver improves phenotype in a murine model of Wilson's 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=4336199
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27 September 2018
Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms
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PubMed Central
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27 September 2018
Iron metabolism and the role of HFE gene polymorphisms in Wilson disease
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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=4336199
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27 September 2018
Criteria for early identification of aceruloplasminemia
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PubMed Central
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27 September 2018
Decreased serum ceruloplasmin levels characteristically aggravate nigral iron deposition in Parkinson’s disease
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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=4336199
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27 September 2018
Evaluation of the symptomatic treatment of residual neurological symptoms in Wilson 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=4336199
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27 September 2018
Do MRI features distinguish Wilson's disease from other early onset extrapyramidal disorders? An analysis of 100 cases.
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=4336199
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27 September 2018
Long-term exclusive zinc monotherapy in symptomatic Wilson disease: experience in 17 patients
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=4336199
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27 September 2018
Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver, by S. A. Kinnier Wilson, (From the National Hospital, and the Laboratory of the National Hospital, Queen Square, London) Brain 1912: 34; 295-509.
1 reference
stated in
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=4336199
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27 September 2018
Neuropsychiatric aspects of treated Wilson's disease.
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=4336199
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27 September 2018
Lower serum ceruloplasmin levels correlate with younger age of onset in Parkinson's disease
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=4336199
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27 September 2018
Longitudinal prognostic value of serum "free" copper in patients with Alzheimer disease.
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=4336199
retrieved
27 September 2018
Evaluation of the Unified Wilson's Disease Rating Scale (UWDRS) in German patients with treated Wilson's disease
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=4336199
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27 September 2018
Successful treatment of tremor in Wilson's disease by thalamotomy: A case report.
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=4336199
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27 September 2018
Dominant psychiatric manifestations in Wilson's disease: a diagnostic and therapeutic challenge!
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=4336199
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27 September 2018
Wilson disease: description of 282 patients evaluated over 3 decades
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=4336199
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27 September 2018
Late-onset Wilson's disease
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=4336199
retrieved
27 September 2018
Homozygosity for a gross partial gene deletion of the C-terminal end of ATP7B in a Wilson patient with hepatic and no neurological manifestations.
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=4336199
retrieved
27 September 2018
Liver transplantation for Wilson's disease: The burden of neurological and psychiatric disorders
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=4336199
retrieved
27 September 2018
Wilson disease in septuagenarian siblings: Raising the bar for diagnosis.
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=4336199
retrieved
27 September 2018
Clinical correlation of brain MRI and MRS abnormalities in patients with Wilson disease
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=4336199
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27 September 2018
Pilot study of mass screening for Wilson's disease in Korea.
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=4336199
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27 September 2018
To test or not? The value of diagnostic tests in cervical dystonia
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=4336199
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27 September 2018
The Wilson disease gene: spectrum of mutations and their consequences
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=4336199
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27 September 2018
Bioinorganic Chemistry of Parkinson’s Disease: Structural Determinants for the Copper-Mediated Amyloid Formation of Alpha-Synuclein
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=4336199
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16 November 2018
PROGRESSIVE LENTICULAR DEGENERATION: A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of His1069Gln and Gly1267Lys mutations in Polish Wilson's disease population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long-term follow-up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oxidative-phosphorylation defects in liver of patients with Wilson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cause of death in Wilson disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dystonia in Wilson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acute extrapyramidal syndrome and seizures as heralding manifestation of Wilson disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diverse attention deficits in patients with neurologically symptomatic and asymptomatic Wilson’s disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Wilson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Zinc monotherapy is not as effective as chelating agents in treatment of Wilson disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic value of quantitative hepatic copper determination in patients with Wilson's Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A study of Wilson disease mutations in Britain
2 references
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25496901
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Meta-Analysis of Serum Non-Ceruloplasmin Copper in Alzheimer's Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The synucleins are a family of redox-active copper binding proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ceruloplasmin oxidation, a feature of Parkinson's disease CSF, inhibits ferroxidase activity and promotes cellular iron retention
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970190-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1474-4422(14)70190-5
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
PMC publication ID
4336199
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
PubMed publication ID
25496901
1 reference
stated in
Europe PubMed Central
PMC publication ID
4336199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25496901%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 June 2020
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