Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.
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Genotype-phenotype correlations of amyotrophic lateral sclerosisExploring new pathways of neurodegeneration in ALS: the role of mitochondria quality controlSearching for a link between the L-BMAA neurotoxin and amyotrophic lateral sclerosis: a study protocol of the French BMAALS programmeMISSING DATA IMPUTATION IN THE ELECTRONIC HEALTH RECORD USING DEEPLY LEARNED AUTOENCODERS.Age-related penetrance of the C9orf72 repeat expansion.Side of limb-onset predicts laterality of gray matter loss in amyotrophic lateral sclerosis.An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report.Genotype-property patient-phenotype relations suggest that proteome exhaustion can cause amyotrophic lateral sclerosis.Observation of c.260A > G mutation in superoxide dismutase 1 that causes p.Asn86Ser in Iranian amyotrophic lateral sclerosis patient and absence of genotype/phenotype correlation.Intraperitoneally administered IgG from patients with amyotrophic lateral sclerosis or from an immune-mediated goat model increase the levels of TNF-α, IL-6, and IL-10 in the spinal cord and serum of mice.Cerebrospinal fluid of newly diagnosed amyotrophic lateral sclerosis patients exhibits abnormal levels of selenium species including elevated selenite.Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.The phenotypic variability of amyotrophic lateral sclerosis.Challenges in the Understanding and Treatment of Amyotrophic Lateral Sclerosis/Motor Neuron Disease.Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin.New ALS-Related Genes Expand the Spectrum Paradigm of Amyotrophic Lateral Sclerosis.Fluid-Based Biomarkers for Amyotrophic Lateral Sclerosis.Supportive care needs of patients with amyotrophic lateral sclerosis/motor neuron disease and their caregivers: A scoping review.Label-Free LC-MS/MS Proteomic Analysis of Cerebrospinal Fluid Identifies Protein/Pathway Alterations and Candidate Biomarkers for Amyotrophic Lateral SclerosisNo evidence of association between polymorphisms in four genes and sporadic amyotrophic lateral sclerosis in Han Chinese.Valproate Treatment in an ALS Patient Carrying a c.194G>A Spastin Mutation and SMN2 Homozygous Deletion.A unique account of ALS in China: exploring ethnic heterogeneity.Amyloid- and FDG-PET imaging in amyotrophic lateral sclerosis.Genetic Counseling Dilemmas for a Patient with Sporadic Amyotrophic Lateral Sclerosis, Frontotemporal Degeneration & Parkinson's Disease.Referral bias in ALS epidemiological studies.
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P2860
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
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artículo científico
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name
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.
@en
type
label
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.
@en
prefLabel
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.
@en
P2860
P356
P1433
P1476
Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.
@en
P2093
P2860
P304
P356
10.1111/CGE.12117
P577
2013-03-12T00:00:00Z