Results 271 to 280 of about 55,413 (307)
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2018
The cerebellum plays an integral role in the control of limb and ocular movements, balance, and walking. Cerebellar disorders may be classified as sporadic or hereditary with clinical presentation varying with the extent and site of cerebellar damage and extracerebellar signs.
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The cerebellum plays an integral role in the control of limb and ocular movements, balance, and walking. Cerebellar disorders may be classified as sporadic or hereditary with clinical presentation varying with the extent and site of cerebellar damage and extracerebellar signs.
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Current Drug Research Reviews
Abstract: Brain-derived neurotrophic factor (BDNF) has been proposed as a treatment for neurodegeneration, including diseases of the cerebellum, where BDNF levels or those of its main receptor, TrkB, are often diminished relative to controls, thereby serving as replacement therapy.
Robert Lalonde +2 more
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Abstract: Brain-derived neurotrophic factor (BDNF) has been proposed as a treatment for neurodegeneration, including diseases of the cerebellum, where BDNF levels or those of its main receptor, TrkB, are often diminished relative to controls, thereby serving as replacement therapy.
Robert Lalonde +2 more
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Cerebellar stimulation in acute cerebellar ataxia
Clinical Neurophysiology, 2001To report follow-up studies of cerebellar stimulation in patients with acute cerebellar ataxia (ACA).We studied two patients with ACA. One patient also had decreased deep sensations in the feet due to combined diseases such as diabetic polyneuropathy and lumbosacral radiculopathies. We applied the technique of electrical stimulation over the cerebellum
K, Matsunaga +3 more
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Seminars in Neurology, 2014
This review broadly covers the commoner genetic ataxias, concentrating on their clinical features. Over the last two decades there has been a potentially bewildering profusion of newly described genetic ataxias. However, at least half of dominant ataxias (SCAs) are caused by (CAG)n repeat expansions resulting in expanded polyglutamine tracts (SCAs 1, 2,
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This review broadly covers the commoner genetic ataxias, concentrating on their clinical features. Over the last two decades there has been a potentially bewildering profusion of newly described genetic ataxias. However, at least half of dominant ataxias (SCAs) are caused by (CAG)n repeat expansions resulting in expanded polyglutamine tracts (SCAs 1, 2,
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Proceedings of the Royal Society of Medicine, 2010
AbstractDisease processes affecting the cerebellum and its connections, such as can occur in multiple sclerosis, often lead to lack of motor coordination, postural tremor, and tremor on directed movement; these symptoms can be difficult to treat. The cerebellum generates oscillations over a range of frequencies (beta, gamma, very fast) and some of ...
Roger D. Roger, Miles A. Whittington
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AbstractDisease processes affecting the cerebellum and its connections, such as can occur in multiple sclerosis, often lead to lack of motor coordination, postural tremor, and tremor on directed movement; these symptoms can be difficult to treat. The cerebellum generates oscillations over a range of frequencies (beta, gamma, very fast) and some of ...
Roger D. Roger, Miles A. Whittington
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A child with cerebellar ataxia
The British Journal of Radiology, 2008S, Gamanagatti, Z, Nayaz
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1997
Abstract Major inroads have now been made by molecular geneticists into the differentiation of the many syndromes of cerebellar ataxia. In general, it is still useful to use age of onset and associated features as a starting point. Congenital onset: cerebellar hypoplasia recessive; cerebellar hypoplasia dominant; cerebellar hypoplasia ...
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Abstract Major inroads have now been made by molecular geneticists into the differentiation of the many syndromes of cerebellar ataxia. In general, it is still useful to use age of onset and associated features as a starting point. Congenital onset: cerebellar hypoplasia recessive; cerebellar hypoplasia dominant; cerebellar hypoplasia ...
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Abstract This chapter deals with disorders of the cerebellum and its connections. These conditions may be identified by the pattern of onset—whether acute, chronic, or episodic. Genetic ataxias are inherited in various patterns: autosomal dominant, autosomal recessive, X-linked. Some episodic ataxias have variable inheritance.
Christopher H. Hawkes +2 more
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Christopher H. Hawkes +2 more
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Acute Cerebellar Ataxia, Acute Cerebellitis, and Opsoclonus-Myoclonus Syndrome
Journal of Child Neurology, 2012Jay Desai
exaly