Results 281 to 290 of about 147,177 (327)
Longitudinal assessment of the upper limb in adults with cerebral palsy
Developmental Medicine &Child Neurology, Volume 68, Issue 4, Page 463-464, April 2026.
Prue Morgan
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Current Treatment Options in Neurology, 2009
Treatment of spasticity requires a team approach, including the patient and caregivers, therapists, physicians, and surgeons. The team needs to determine what component of the spasticity interferes with function. Traditional therapy continues to dominate the therapy provided to patients who are living with spasticity.
Allison, Brashear, Kelly, Lambeth
+6 more sources
Treatment of spasticity requires a team approach, including the patient and caregivers, therapists, physicians, and surgeons. The team needs to determine what component of the spasticity interferes with function. Traditional therapy continues to dominate the therapy provided to patients who are living with spasticity.
Allison, Brashear, Kelly, Lambeth
+6 more sources
Journal of Neurotrauma, 2020
Epidural spinal cord stimulation (SCS) is currently regarded as a breakthrough procedure for enabling movement after spinal cord injury (SCI), yet one of its original applications was for spinal spasticity.
U. Hofstoetter +6 more
semanticscholar +1 more source
Epidural spinal cord stimulation (SCS) is currently regarded as a breakthrough procedure for enabling movement after spinal cord injury (SCI), yet one of its original applications was for spinal spasticity.
U. Hofstoetter +6 more
semanticscholar +1 more source
2012
Antispastic medications that are directed to reduce clinical signs of spasticity, such as exaggerated reflexes and muscle tone, do not improve the movement disorder. Medication can even increase weakness which might interfere with functional movements, such as walking.
Dietz, Volker, Sinkjaer, Thomas
+6 more sources
Antispastic medications that are directed to reduce clinical signs of spasticity, such as exaggerated reflexes and muscle tone, do not improve the movement disorder. Medication can even increase weakness which might interfere with functional movements, such as walking.
Dietz, Volker, Sinkjaer, Thomas
+6 more sources
Clinical Orthopaedics and Related Research, 1987
Spasticity has been defined as velocity-dependent hyperactivity of stretch reflexes; it is therefore only one aspect of the complex syndrome produced by a lesion of the upper motoneuron. Although spasticity may be partially responsible for joint contractures, it does not produce most of the functional disability experienced by patients with upper ...
R R, Young, A W, Wiegner
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Spasticity has been defined as velocity-dependent hyperactivity of stretch reflexes; it is therefore only one aspect of the complex syndrome produced by a lesion of the upper motoneuron. Although spasticity may be partially responsible for joint contractures, it does not produce most of the functional disability experienced by patients with upper ...
R R, Young, A W, Wiegner
openaire +2 more sources
International Journal of Neuroscience, 2018
Purpose/aim: To evaluate the efficacy of tetrahydrocannabinol (THC):cannabidiol (CBD) oromucosal spray (Sativex®) as add-on therapy to optimised standard antispasticity treatment in patients with moderate to severe multiple sclerosis (MS) spasticity ...
J. Marková +6 more
semanticscholar +1 more source
Purpose/aim: To evaluate the efficacy of tetrahydrocannabinol (THC):cannabidiol (CBD) oromucosal spray (Sativex®) as add-on therapy to optimised standard antispasticity treatment in patients with moderate to severe multiple sclerosis (MS) spasticity ...
J. Marková +6 more
semanticscholar +1 more source
Journal of the American Medical Association, 1934
Spastic paraplegia is a descriptive term and not a diagnosis. Its causes are many. In the classic form it is characterized by a progressive spasticity in the lower limbs, with all the signs and symptoms of a pyramidal tract disease below the level of the lesion. The onset is described by the patient in terms of fatigability of the lower limbs.
N. W. Winkelman, John L. Eckel
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Spastic paraplegia is a descriptive term and not a diagnosis. Its causes are many. In the classic form it is characterized by a progressive spasticity in the lower limbs, with all the signs and symptoms of a pyramidal tract disease below the level of the lesion. The onset is described by the patient in terms of fatigability of the lower limbs.
N. W. Winkelman, John L. Eckel
openaire +1 more source
2018
The presence of spasticity and pyramidal features is a hallmark of some of hereditary ataxias, such as autosomal-recessive spastic ataxia of Charlevoix-Saguenay, other primary spastic ataxias, Friedreich ataxia, or ataxia with isolated vitamin E deficiency.
Olena, Bereznyakova, Nicolas, Dupré
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The presence of spasticity and pyramidal features is a hallmark of some of hereditary ataxias, such as autosomal-recessive spastic ataxia of Charlevoix-Saguenay, other primary spastic ataxias, Friedreich ataxia, or ataxia with isolated vitamin E deficiency.
Olena, Bereznyakova, Nicolas, Dupré
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Annals of Otology, Rhinology & Laryngology, 1976
130 cases of spastic dysphonia are reviewed with special emphasis on the etiology of the disorder. An analysis of the circumstances surrounding the onset of the disease points strongly to a psychogenic origin of the disease in, at least, the vast majority of the cases.
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130 cases of spastic dysphonia are reviewed with special emphasis on the etiology of the disorder. An analysis of the circumstances surrounding the onset of the disease points strongly to a psychogenic origin of the disease in, at least, the vast majority of the cases.
openaire +2 more sources
Neurologic Clinics, 2002
The hereditary spastic paraplegias (HSPs) comprise a large group of inherited neurologic disorders. HSP is classified according to the mode of inheritance, the HSP locus when known, and whether the spastic paraplegia syndrome occurs alone or is accompanied by additional neurologic or systemic abnormalities.
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The hereditary spastic paraplegias (HSPs) comprise a large group of inherited neurologic disorders. HSP is classified according to the mode of inheritance, the HSP locus when known, and whether the spastic paraplegia syndrome occurs alone or is accompanied by additional neurologic or systemic abnormalities.
openaire +3 more sources