Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
about
Creatine for amyotrophic lateral sclerosis/motor neuron diseaseCreatine for amyotrophic lateral sclerosis/motor neuron diseaseNeuroimaging to investigate multisystem involvement and provide biomarkers in amyotrophic lateral sclerosisImpact of presymptomatic genetic testing for familial amyotrophic lateral sclerosis.Neurotoxic mechanisms of degeneration in motor neuron diseases.British motor neuron disease twin study.Disease-related changes in the cerebrospinal fluid metabolome in amyotrophic lateral sclerosis detected by GC/TOFMS.Genetic heterogeneity of amyotrophic lateral sclerosis: implications for clinical practice and research.Patterns of spontaneous brain activity in amyotrophic lateral sclerosis: a resting-state FMRI studyAmyotrophic lateral sclerosis: update and new developments.Intricate interplay between astrocytes and motor neurons in ALS.Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group.Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features.Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.Juvenile and adult-onset ALS/MND among Africans: incidence, phenotype, survival: a review.CSF markers in amyotrophic lateral sclerosis.Proteome analysis of body fluids for amyotrophic lateral sclerosis biomarker discovery.Proteomic studies in the discovery of cerebrospinal fluid biomarkers for amyotrophic lateral sclerosis.Beyond muscles: The untapped potential of creatine.Reproductive decision-making among individuals at risk for familial amyotrophic lateral sclerosis.Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis.SOD1 gene mutations in ALS patients from British Columbia, Canada: clinical features, neurophysiology and ethical issues in management.Apparent anticipation in SOD1 familial amyotrophic lateral sclerosis.Nocturnal pulse oximetry: a new approach to establish the appropriate time for non-invasive ventilation in ALS patients.Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotypeMulticentre quality control evaluation of different biomarker candidates for amyotrophic lateral sclerosis
P2860
Q24202577-111DC3A6-360E-4984-8E07-087489A813E8Q24234800-AB0FDC64-C568-472A-8B32-C13E3D4945FFQ30832443-5BB3A1F5-886B-4E10-A0B9-366F3233A562Q33687938-16C6EB89-85A5-4A56-AFD6-276AA670A345Q33719819-D501E768-0FAE-463C-A2DF-E02501917B0DQ33735812-DEB1FF5B-6B71-4E26-B404-757B4DD5CA7BQ33869419-1B1F1B08-7647-4E91-95A6-DB6E3475D6AFQ34401653-87F0DE13-DABB-4322-8658-2F6B873CDF04Q34429131-E1B67A6F-A9B0-49C3-8E5B-076299934C91Q36278310-AE8B3724-A653-4DB0-B080-000F7322AD8AQ36637458-4067B60F-71E9-478A-9394-1E5E22AD5B32Q36892306-E217FDF0-5DBC-42C1-97A5-BA6402353DE4Q36899693-DFE4769F-D1C4-4428-82A2-4F7DADB8621BQ37688651-23C9CCE4-0309-4A19-B844-2AF1188683C5Q38005425-73061BED-0506-4F9F-81A6-66CC870CA3E1Q38007362-37F09CE4-6FE1-4B11-8604-601E07C660ECQ38058054-267AE9F3-EDD9-44FE-8D1F-06A66DE47891Q38643847-1F4A34EC-11CB-4118-BBA1-1F291EE4D29BQ38700215-5883AB0E-F90D-408E-B286-EC2C20D9C53CQ39131879-E8544963-4DED-44B4-943C-D3C764B2189FQ42765711-4985E63E-582C-4BF5-875C-45F673E08C92Q44317932-70829E1E-C1EC-48A0-915B-3018A5B3EA6EQ44956628-AB518C60-6FBE-4F6C-9ABE-E9D4962D2BA5Q45883983-ED633240-D892-4048-8208-86A1BCA33C6FQ48628445-CA2CDD30-CFCA-40F4-897D-4DE496B4C678Q57085780-5D430BA2-DFA0-4D9B-8FC7-F90216F223E2Q58181716-A45D9824-6C74-41E5-AC7A-D19901D48765
P2860
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
description
1988 nî lūn-bûn
@nan
1988 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
@ast
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
@en
type
label
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
@ast
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
@en
prefLabel
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
@ast
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
@en
P2093
P2860
P356
P1476
Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease.
@en
P2093
P2860
P304
P356
10.1136/JNNP.51.6.778
P407
P577
1988-06-01T00:00:00Z