Sporadic lower motor neuron disease with adult onset: classification of subtypes.
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Pathways and genes differentially expressed in the motor cortex of patients with sporadic amyotrophic lateral sclerosisCold paresis in multifocal motor neuropathyIntake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosisStudy of 962 patients indicates progressive muscular atrophy is a form of ALS.Axon loss is an important determinant of weakness in multifocal motor neuropathy.Klinefelter's syndrome associated with progressive muscular atrophy simulating Kennedy's diseaseAnaesthesia for ophthalmologic surgical procedures in a patient with advanced amyotrophic lateral sclerosis: a case report.Electrophysiology in demyelinating polyneuropathies.Multifocal motor neuropathy: diagnosis, pathogenesis and treatment strategies.Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in amyotrophic lateral sclerosis (ALS).Facial Onset Sensory and Motor Neuronopathy: Further Evidence for a TDP-43 Proteinopathy.A woman with forearm amyotrophy.Fast progressive lower motor neuron disease is an ALS variant: A two-centre tract of interest-based MRI data analysis.Monomelic amyotrophy is not always benign: a case report.SMN1 gene duplications are more frequent in patients with progressive muscular atrophy.Meta-analysis of gene expression profiling in amyotrophic lateral sclerosis: a comparison between transgenic mouse models and human patients.Patterns of symptom development in patients with motor neuron disease.Prospective, blind study of the triple stimulation technique in the diagnosis of ALS.Corticoefferent pathways in pure lower motor neuron disease: a diffusion tensor imaging study.Cortical thickness in ALS: towards a marker for upper motor neuron involvement.Fasciculation potentials in amyotrophic lateral sclerosis and the diagnostic yield of the Awaji algorithm.Paraneoplastic motor neuron disease associated with breast cancer.Amyotrophic lateral sclerosisClinical patterns in progressive muscular atrophy (PMA): a prospective studyMRI-Based Mapping of Cerebral Propagation in Amyotrophic Lateral SclerosisThe El Escorial criteria: Strengths and weaknesses
P2860
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P2860
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
description
2003 nî lūn-bûn
@nan
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
@ast
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
@en
type
label
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
@ast
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
@en
prefLabel
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
@ast
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
@en
P2093
P356
P1433
P1476
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
@en
P2093
Franssen H
de Jong JM
de Visser M
van den Berg LH
van den Berg-Vos RM
P304
P356
10.1093/BRAIN/AWG117
P407
P577
2003-05-01T00:00:00Z