Results 341 to 350 of about 166,105 (376)
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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.
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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.
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2015
Abstract This is a chapter on Spasticity from the Upper Motor Neuron disorders section of A Manual of Neurological Signs. Most of the chapters contain a description of the sign, associated signs, and cases, supported by clinical videos and figures.
John G. Morris, Padraic J. Grattan-Smith
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Abstract This is a chapter on Spasticity from the Upper Motor Neuron disorders section of A Manual of Neurological Signs. Most of the chapters contain a description of the sign, associated signs, and cases, supported by clinical videos and figures.
John G. Morris, Padraic J. Grattan-Smith
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Spinal Cord Stimulation for Spasticity: Historical Approaches, Current Status, and Future Directions
Neuromodulation (Malden, Mass.), 2017Millions of people worldwide suffer with spasticity related to irreversible damage to the brain or spinal cord. Typical antecedent events include stroke, traumatic brain injury, and spinal cord injury, although insidious onset is also common.
S. Nagel +8 more
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Professional nurse (London, England), 1999
Spasticity affects people with a variety of conditions, including stroke, spinal cord injury and multiple sclerosis. Assessment, physical therapies and pharmacological and invasive treatments are discussed in this Update.
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Spasticity affects people with a variety of conditions, including stroke, spinal cord injury and multiple sclerosis. Assessment, physical therapies and pharmacological and invasive treatments are discussed in this Update.
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Management of spasticity in hereditary spastic paraplegia
Physiotherapy Research International, 1999D, Richardson, A J, Thompson
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