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1 sis (neurodegeneration) in different genetic motor neuron disorders'.
2 eral sclerosis (ALS) is a fatal degenerative motor neuron disorder.
3 trophic lateral sclerosis is the most common motor neuron disorder.
4 that at presentation could be mistaken for a motor neuron disorder.
5 ditary Spastic Paraplegia called NTE-related Motor-Neuron Disorder.
6 potential of gene replacement therapies for motor neuron disorders.
7 PLS and ALS behave as part of a continuum of motor neuron disorders.
8 callosal neurons within the motor cortex in motor neuron disorders.
9 d have relevance to sensory neuropathies and motor neuron disorders.
11 is known to be a pathogenic mechanism in the motor neuron disorder amyotrophic lateral sclerosis (ALS
12 amyotrophic lateral sclerosis (ALS), a fatal motor neuron disorder, and frontotemporal lobar degenera
13 t lacking both SMNT exons showed no signs of motor neuron disorder by clinical and neurodiagnostic an
14 al spinal muscular atrophy (SMA) is a common motor neuron disorder caused by mutation of the telomeri
15 yotrophic lateral sclerosis (ALS) is a fatal motor neuron disorder characterized pathologically by ub
16 hly heterogeneous group of neurodegenerative motor neuron disorders characterized by spastic parapare
17 diagnosed with PLS referred to a specialised motor neuron disorders clinic from 2002 to 2024, analyse
19 are associated with the inherited peripheral motor neuron disorders distal hereditary motor neuropath
20 ifferential vulnerability to degeneration in motor neuron disorders, identified enriched transcripts
22 of patients with a suspected diagnosis of a motor neuron disorder (n = 119; mean age +/- SD, 61 +/-
23 n HMN/CMT2 genes may also be responsible for motor neuron disorders or other neuromuscular diseases,
27 otein triggers the oft-fatal infantile-onset motor neuron disorder, spinal muscular atrophy (SMA).