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Paresis

Known as: Pareses, Muscle, Muscle Paresis, Paresis, Muscular 
A general term referring to a mild to moderate degree of muscular weakness, occasionally used as a synonym for PARALYSIS (severe or complete loss of… Expand
National Institutes of Health

Related topics

Related topics

35 relations
(non-specific) malaise and fatigueActual DiscomfortAsthenic personalityCongenital debility NOS
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Narrower (8)

Encephalopathy, Spastic Tetraparesis, and HypogonadismHemiparesisHhhh SyndromeLower Extremity Paresis
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Broader (2)

Symptomsnervous system disorder

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Disrupted neuronal trafficking in amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a progressive, adult-onset neurodegenerative disease caused by degeneration of motor… Expand
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Review
2017
Review
2017
Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration
Amyotrophic lateral sclerosis (ALS) is a disease caused by the degeneration of motor neurons (MNs) leading to progressive muscle… Expand
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Review
2017
Review
2017
Nusinersen for the treatment of spinal muscular atrophy
  • C. Chiriboga
  • Expert review of neurotherapeutics
  • 2017
    • Corpus ID: 34129545
ABSTRACT Introduction: Spinal muscular atrophy (SMA) is an autosomal recessive degenerative neuromuscular disorder characterized… Expand
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Highly Cited
2009
Highly Cited
2009
Induced pluripotent stem cells from a spinal muscular atrophy patient
Spinal muscular atrophy is one of the most common inherited forms of neurological disease leading to infant mortality. Patients… Expand
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Highly Cited
2002
Highly Cited
2002
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
The Charcot-Marie-Tooth (CMT) disorders comprise a group of clinically and genetically heterogeneous hereditary motor and sensory… Expand
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Highly Cited
2001
Highly Cited
2001
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
BACKGROUND Familial hemiplegic migraine, an autosomal dominant disorder characterized by attacks of transient hemiparesis… Expand
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Highly Cited
2000
Highly Cited
2000
Cortical motor reorganization in akinetic patients with Parkinson's disease: a functional MRI study.
Using functional MRI (fMRI), we have studied the changes induced by the performance of a complex sequential motor task in the… Expand
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Highly Cited
1992
Highly Cited
1992
Hemidiaphragmatic paresis during interscalene brachial plexus block: effects on pulmonary function and chest wall mechanics.
We studied the effects of unilateral hemidiaphragmatic paresis caused by interscalene brachial plexus block on routine pulmonary… Expand
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Highly Cited
1991
Highly Cited
1991
One Hundred Percent Incidence of Hemidiaphragmatic Paresis Associated With Interscalene Brachial Plexus Anesthesia as Diagnosed by Ultrasonography
Interscalene brachial plexus anesthesia for shoulder surgery routinely includes sensory anesthesia of the fourth and fifth… Expand
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Highly Cited
1990
Highly Cited
1990
Arm and leg paresis as outcome predictors in stroke rehabilitation.
I used leg and arm paresis to predict outcome measured as extremity function in a prospective study of 75 consecutive hemiplegic… Expand
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