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Paresis
Known as:
Pareses, Muscle
, Muscle Paresis
, Paresis, Muscular
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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…
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National Institutes of Health
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Related topics
Related topics
35 relations
(non-specific) malaise and fatigue
Actual Discomfort
Asthenic personality
Congenital debility NOS
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Narrower (8)
Encephalopathy, Spastic Tetraparesis, and Hypogonadism
Hemiparesis
Hhhh Syndrome
Lower Extremity Paresis
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Broader (2)
Symptoms
nervous system disorder
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Induced pluripotent stem cells from a spinal muscular atrophy patient
A. Ebert
,
Junying Yu
,
+4 authors
C. Svendsen
Nature
2009
Corpus ID: 4399268
Spinal muscular atrophy is one of the most common inherited forms of neurological disease leading to infant mortality. Patients…
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Review
2005
Review
2005
Pathophysiology of spastic paresis. I: Paresis and soft tissue changes
J. Gracies
Muscle & nerve
2005
Corpus ID: 24232176
Spastic paresis follows chronic disruption of the central execution of volitional command. Motor function in patients with…
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Review
2005
Review
2005
Response of brain tissue to chronically implanted neural electrodes
Vadim S. Polikov
,
P. Tresco
,
W. Reichert
Journal of Neuroscience Methods
2005
Corpus ID: 11248506
Review
2005
Review
2005
Pathophysiology of spastic paresis. II: Emergence of muscle overactivity
J. Gracies
Muscle & nerve
2005
Corpus ID: 41590510
In the subacute and chronic stages of spastic paresis, stretch‐sensitive (spastic) muscle overactivity emerges as a third…
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Review
2003
Review
2003
Experiential Avoidance and Behavioral Disorders: A Functional Dimensional Approach to Diagnosis and Treatment
S. Haves
,
K. Wilson
,
K. Strosahl
,
E. Gifford
,
V. Follette
2003
Corpus ID: 2267144
Syndromal classification is a well-developed diagnostic system but has failed to deliver on its promise of the identification of…
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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.
A. De Sandre-Giovannoli
,
M. Chaouch
,
+9 authors
N. Lévy
American journal of human genetics
2002
Corpus ID: 25211812
The Charcot-Marie-Tooth (CMT) disorders comprise a group of clinically and genetically heterogeneous hereditary motor and sensory…
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Highly Cited
2001
Highly Cited
2001
Axon-Glia Interactions and the Domain Organization of Myelinated Axons Requires Neurexin IV/Caspr/Paranodin
M. Bhat
,
J. C. Rios
,
+9 authors
H. Bellen
Neuron
2001
Corpus ID: 10746863
Highly Cited
1995
Highly Cited
1995
Recovery of walking function in stroke patients: the Copenhagen Stroke Study.
H. S. Jørgensen
,
H. Nakayama
,
H. Raaschou
,
T. Olsen
Archives of physical medicine and rehabilitation
1995
Corpus ID: 37201542
Highly Cited
1994
Highly Cited
1994
Recovery of upper extremity function in stroke patients: the Copenhagen Stroke Study.
H. Nakayama
,
H. S. Jørgensen
,
H. Raaschou
,
T. Olsen
Archives of physical medicine and rehabilitation
1994
Corpus ID: 42700407
Highly Cited
1992
Highly Cited
1992
Hemidiaphragmatic paresis during interscalene brachial plexus block: effects on pulmonary function and chest wall mechanics.
W. Urmey
,
M. McDonald
Anesthesia and analgesia
1992
Corpus ID: 34952859
We studied the effects of unilateral hemidiaphragmatic paresis caused by interscalene brachial plexus block on routine pulmonary…
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