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Presymptomatic studies in ALS: rationale, challenges, and approach
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PubMed
title
Presymptomatic studies in ALS: rationale, challenges, and approach
(English)
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stated in
PubMed
main subject
amyotrophic lateral sclerosis
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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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PubMed
volume
79
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stated in
PubMed
issue
16
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PubMed
page(s)
1732-9
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PubMed
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
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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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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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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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TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
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Preventing familial amyotrophic lateral sclerosis: is a clinical trial feasible?
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Detection of preclinical motor neurone loss in SOD1 mutation carriers using motor unit number estimation
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Normal complement of motor units in asymptomatic familial (SOD1 mutation) amyotrophic lateral sclerosis carriers
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The motor cortex and amyotrophic lateral sclerosis
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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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Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis
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Implications of ALS focality: rostral-caudal distribution of lower motor neuron loss postmortem
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28 November 2018
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28 November 2018
Incidence of ALS in Lombardy, Italy
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28 November 2018
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28 November 2018
"You have shown me my end": attitudes toward presymptomatic testing for familial amyotrophic lateral sclerosis
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23071166
retrieved
12 December 2020
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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
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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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