Results 311 to 320 of about 117,087 (348)
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1984
There are various conditions in which involuntary movements develop and in which pathological changes are present in the basal ganglia. Some of these conditions, and especially paralysis agitans, have been the subject of intense study during the past two decades.
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There are various conditions in which involuntary movements develop and in which pathological changes are present in the basal ganglia. Some of these conditions, and especially paralysis agitans, have been the subject of intense study during the past two decades.
openaire +1 more source
Biotin Thiamin Responsive Basal Ganglia Disease in Siblings
The Indian Journal of Pediatrics, 2017Biotin Thiamine responsive Basal Ganglia Disease (BTBGD) is a rare treatable autosomal recessive metabolic disorder caused by mutations in SLC19A3 gene. It usually presents with encephalopathy and dystonia; if not treated, can progress to quadriparesis and death.
Vykuntaraju K, Gowda +3 more
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Idiopathic Basal Ganglia Calcifications and Parkinson's Disease
The American Journal of Medicine, 2022Xiaopeng, Guo +3 more
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment
Ca-A Cancer Journal for Clinicians, 2022Jun J Mao,, Msce +2 more
exaly
Motor disorders in basal ganglia disease.
Human neurobiology, 1984The clinical motor symptoms of basal ganglia disease are explored in relation to possible functions of this region of the human brain. It is concluded that Parkinsonian akinesia, and the dyskinesias of chorea, hemiballism and torsion dystonia are likely to represent the critical abnormalities of motor action in human basal ganglia lesions.
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Psychiatric Consequences of Basal Ganglia Disease
Seminars in Neurology, 1990openaire +2 more sources