Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
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From animal models to human disease: a genetic approach for personalized medicine in ALSIn Vivo Confocal Microscopy of the Human Cornea in the Assessment of Peripheral Neuropathy and Systemic DiseasesALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the diseaseSelective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis.Patterns of spontaneous brain activity in amyotrophic lateral sclerosis: a resting-state FMRI studyElectrophysiological and spinal imaging evidences for sensory dysfunction in amyotrophic lateral sclerosisAutonomic system and amyotrophic lateral sclerosis.Visualization of Sensory Neurons and Their Projections in an Upper Motor Neuron Reporter Line.Depression, pain and quality of life in patients with amyotrophic lateral sclerosis: a cross-sectional study.Clinical neurogenetics: amyotrophic lateral sclerosis.ALS drug development: reflections from the past and a way forwardLaryngeal Sensitivity in Patients with Amyotrophic Lateral Sclerosis.SOD1 and TDP-43 animal models of amyotrophic lateral sclerosis: recent advances in understanding disease toward the development of clinical treatments.Muscle wasting from kidney failure-a model for catabolic conditions.The non-cell-autonomous component of ALS: new in vitro models and future challenges.Is there pain with neuropathic characteristics in patients with amyotrophic lateral sclerosis? A cross-sectional study.Topography of FUS pathology distinguishes late-onset BIBD from aFTLD-U.Corneal confocal microscopy reveals trigeminal small sensory fiber neuropathy in amyotrophic lateral sclerosis.Concomitant amyotrophic lateral sclerosis and paraclinical laboratory features of multiple sclerosis: coincidence or causal relationship?Vasculitis-like neuropathy in amyotrophic lateral sclerosis unresponsive to treatment.Degeneration of proprioceptive sensory nerve endings in mice harboring amyotrophic lateral sclerosis-causing mutations.An exploratory study of the association between thyroid hormone and survival of amyotrophic lateral sclerosis.Association of amyotrophic lateral sclerosis and Behcet's disease: is there a relationship? A multi-national case series.Involvement of spinal sensory pathway in ALS and specificity of cord atrophy to lower motor neuron degeneration.Escape from homeostasis: spinal microcircuits and progression of amyotrophic lateral sclerosis.Beyond weakness: Characterization of pain, sensory profile and conditioned pain modulation in patients with motor neuron disease: A controlled study.Molecular mechanisms underlying monosynaptic sensory-motor circuit development in the spinal cord.CSF hypocretin-1 levels are normal in patients with amyotrophic lateral sclerosis.Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport.Involvement of distal sensory nerves in amyotrophic lateral sclerosis.Optical coherence tomography does not support optic nerve involvement in amyotrophic lateral sclerosis.Non-motor involvement in amyotrophic lateral sclerosis: new insight from nerve and vessel analysis in skin biopsy.Involvement of sensory innervation in the skin of SOD1(G93A) ALS mice.Antioxidant and Cell-Signaling Functions of Hydrogen Sulfide in the Central Nervous System.The selective anatomical vulnerability of ALS: ‘disease-defining’ and ‘disease-defying’ brain regionsVariation in the neurophysiological examination of amyotrophic lateral sclerosis in EuropeUltra-High Field Diffusion MRI Reveals Early Axonal Pathology in Spinal Cord of ALS miceClinical analysis and outcomes of amyotrophic lateral sclerosis with demyelinating polyneuropathyThe ALS-inducing factors, TDP43 and SOD1, directly affect and sensitize sensory neurons to stress
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Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 2007
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
@en
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
@nl
type
label
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
@en
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
@nl
prefLabel
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
@en
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
@nl
P2093
P1433
P1476
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.
@en
P2093
P304
P356
10.1212/01.WNL.0000286948.99150.16
P407
P577
2007-12-01T00:00:00Z