Patterns of clinical and electrodiagnostic abnormalities in early amyotrophic lateral sclerosis

scientific article published on 31 October 2014

Patterns of clinical and electrodiagnostic abnormalities in early amyotrophic lateral sclerosis is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/MUS.24244
P698PubMed publication ID24647900
P5875ResearchGate publication ID260947579

P50authorCatherine Lomen-HoerthQ63214706
Matthew C KiernanQ75660683
P2093author name stringNeil G Simon
P2860cites workEl Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosisQ29619074
Dissociated small hand muscle atrophy in amyotrophic lateral sclerosis: frequency, extent, and specificityQ34743713
Statistical motor unit number estimation: from theory to practiceQ35203385
Pattern of spread and prognosis in lower limb-onset ALS.Q35239043
Controversies and priorities in amyotrophic lateral sclerosisQ36045826
Electrodiagnostic criteria for diagnosis of ALS.Q37046933
Stages of pTDP-43 pathology in amyotrophic lateral sclerosisQ37202139
Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insightsQ37206683
ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degenerationQ37593829
Clinical diagnosis and management of amyotrophic lateral sclerosisQ37944429
The split hand syndrome in amyotrophic lateral sclerosisQ37958539
The puzzling case of hyperexcitability in amyotrophic lateral sclerosis.Q38102695
Natural history of ALS: symptoms, strength, pulmonary function, and disabilityQ41152646
Split-hand index for the diagnosis of amyotrophic lateral sclerosisQ43698165
Onset and spreading patterns of lower motor neuron involvements predict survival in sporadic amyotrophic lateral sclerosisQ44833528
Focality of upper and lower motor neuron degeneration at the clinical onset of ALS.Q44929155
Implications of ALS focality: rostral-caudal distribution of lower motor neuron loss postmortemQ44929159
Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosisQ45291121
Split-hand plus sign in ALS: differential involvement of the flexor pollicis longus and intrinsic hand musclesQ45332967
Fasciculation anxiety syndrome in cliniciansQ46589131
Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosisQ48881997
Amyotrophic lateral sclerosis: oxidative energy metabolism and calcium homeostasis in peripheral blood lymphocytesQ48910244
Cortical excitability distinguishes ALS from mimic disorders.Q50686089
Amyotrophic lateral sclerosisQ55877676
Distal motor axonal dysfunction in amyotrophic lateral sclerosisQ56771891
Does the motor cortex influence denervation in ALS? EMG studies of muscles with both contralateral and bilateral corticospinal innervationQ56929689
Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis?Q57498880
P433issue6
P921main subjectamyotrophic lateral sclerosisQ206901
P304page(s)894-899
P577publication date2014-10-31
P1433published inMuscle and NerveQ15764281
P1476titlePatterns of clinical and electrodiagnostic abnormalities in early amyotrophic lateral sclerosis
P478volume50

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cites work (P2860)
Q41708271A functional scale for spinal and bulbar muscular atrophy: Cross-sectional and longitudinal study
Q40957607Accrued somatic mutations (nucleic acid changes) trigger ALS: 2005-2015 update
Q35046924Diffusion weighted MRI and tractography for evaluating peripheral nerve degeneration and regeneration
Q53556253Dissociated lower limb muscle involvement in amyotrophic lateral sclerosis.
Q38597450Motor neuron disease: current management and future prospects
Q51272870Needle electromyography of the frontalis muscle in patients with amyotrophic lateral sclerosis.
Q38985422Optimizing muscle selection for electromyography in amyotrophic lateral sclerosis
Q36760958Pattern Differences of Small Hand Muscle Atrophy in Amyotrophic Lateral Sclerosis and Mimic Disorders
Q50980538Peripheral nerve diffusion tensor imaging is reliable and reproducible.
Q35008605Quantifying disease progression in amyotrophic lateral sclerosis
Q46093112Quantitative ultrasound of denervated hand muscles
Q36251203Relationship between Clinical Parameters and Brain Structure in Sporadic Amyotrophic Lateral Sclerosis Patients According to Onset Type: A Voxel-Based Morphometric Study
Q53188798Split-hand phenomenon in amyotrophic lateral sclerosis: A motor unit number index study.
Q48671390Tracking motor neuron loss in a set of six muscles in amyotrophic lateral sclerosis using the Motor Unit Number Index (MUNIX): a 15-month longitudinal multicentre trial.