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Presymptomatic studies in ALS: rationale, challenges, and approach
scientific article
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scholarly article
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PubMed
title
Presymptomatic studies in ALS: rationale, challenges, and approach
(English)
1 reference
stated in
PubMed
main subject
amyotrophic lateral sclerosis
1 reference
based on heuristic
inferred from title
author name string
M. Benatar
series ordinal
1
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stated in
Crossref
J. Wuu
series ordinal
2
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stated in
Crossref
language of work or name
English
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stated in
PubMed
publication date
16 October 2012
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stated in
PubMed
published in
Neurology
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stated in
PubMed
volume
79
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PubMed
issue
16
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PubMed
page(s)
1732-9
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PubMed
cites work
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
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PubMed Central
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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
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PubMed Central
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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
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Exome sequencing reveals VCP mutations as a cause of familial ALS
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7 April 2017
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
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PubMed Central
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7 April 2017
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
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Hypothetical model of dynamic biomarkers of the Alzheimer's pathological cascade
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Presymptomatic spinal cord neurometabolic findings in SOD1-positive people at risk for familial ALS.
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Multipoint incremental motor unit number estimation as an outcome measure in ALS.
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Impact of presymptomatic genetic testing for familial amyotrophic lateral sclerosis
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Tapping linked to function and structure in premanifest and symptomatic Huntington disease
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Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis
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28 September 2017
Electrical impedance myography: Background, current state, and future directions
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ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration
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Incidence of amyotrophic lateral sclerosis in Europe
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28 September 2017
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
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Detection of Huntington's disease decades before diagnosis: the Predict-HD study
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Association of olfactory dysfunction with risk for future Parkinson's disease
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Preventing familial amyotrophic lateral sclerosis: is a clinical trial feasible?
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28 September 2017
Detection of preclinical motor neurone loss in SOD1 mutation carriers using motor unit number estimation
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PubMed Central
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28 September 2017
Normal complement of motor units in asymptomatic familial (SOD1 mutation) amyotrophic lateral sclerosis carriers
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PubMed Central
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28 September 2017
The motor cortex and amyotrophic lateral sclerosis
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28 September 2017
Amyotrophic lateral sclerosis: lower motor neuron disease spreading to upper motor neurons
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Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
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Measuring the rate of progression and estimating the preclinical period of Parkinson's disease with [18F]dopa PET.
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Epidemiology of ALS in Italy: a 10-year prospective population-based study.
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Increasing incidence of ALS in Canterbury, New Zealand: a 22-year study
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28 November 2018
Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis.
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28 November 2018
Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004.
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28 November 2018
Implications of ALS focality: rostral-caudal distribution of lower motor neuron loss postmortem
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28 November 2018
Focality of upper and lower motor neuron degeneration at the clinical onset of ALS.
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=3468777
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28 November 2018
Incidence of ALS in Lombardy, Italy.
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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=3468777
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28 November 2018
Delayed emergence of a parkinsonian disorder in 38% of 29 older men initially diagnosed with idiopathic rapid eye movement sleep behaviour disorder.
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PubMed Central
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28 November 2018
World Federation of Neurology: Research Committee. Research Group on Huntington's chorea. Ethical issues policy statement on Huntington's disease molecular genetics predictive test
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28 November 2018
"You have shown me my end": attitudes toward presymptomatic testing for familial amyotrophic lateral sclerosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23071166
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Abnormal diffusion tensor in nonsymptomatic familial amyotrophic lateral sclerosis with a causative superoxide dismutase 1 mutation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23071166
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Prevalence of SOD1 mutations in the Italian ALS population
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23071166
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1212/WNL.0B013E31826E9B1D
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4674799
OpenCitations bibliographic resource ID
4674799
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4674799
PMC publication ID
3468777
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4674799
PubMed publication ID
23071166
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4674799
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