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期刊名:Cerebellum and ataxias

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ISSN:2053-8871

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共收录本刊相关文章索引137
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Roman Schniepp,Michael Strupp,Max Wuehr et al. Roman Schniepp et al.
Acetyl-DL-leucine is a modified amino acid that was observed to improve ataxic symptoms in patients with sporadic and hereditary forms of ataxia. Here, we investigated the effect of the treatment with Acetyl-DL-leucine on the walking stabil...
Jan Cendelin Jan Cendelin
Hereditary cerebellar degenerations are a heterogeneous group of diseases often having a detrimental impact on patients' quality of life. Unfortunately, no sufficiently effective causal therapy is available for human patients at present. Th...
Carlotta Lega,Tomaso Vecchi,Egidio D&#x;Angelo et al. Carlotta Lega et al.
Background: Growing neuroimaging and clinical evidence suggests that the cerebellum plays a critical role in perception. In the auditory domain, the cerebellum seems to be important in different aspects of music and sound...
Ashwini K Rao,Elan D Louis Ashwini K Rao
Background: Essential tremor (ET) is a common movement disorder characterized by kinetic, postural and intention tremors. Mounting evidence suggests an underlying dysfunction of the cerebellum or cerebellar system. While ...
Irene Pulido-Valdeolivas,David Gómez-Andrés,Irene Sanz-Gallego et al. Irene Pulido-Valdeolivas et al.
Background: Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder that affects the cerebellar system and other subcortical regions of the brain. As for other cerebellar diseases, the severity of this type o...
Jeanette Koht,Sven Olav Løstegaard,Iselin Wedding et al. Jeanette Koht et al.
Background: Benign hereditary chorea is a rare disorder which is characterized by early onset, non-progressive choreic movement disturbance, with other hyperkinetic movements and unsteadiness also commonly seen. Hypothyro...
M I Shadrina,M V Shulskaya,S A Klyushnikov et al. M I Shadrina et al.
Background: Spinocerebellar ataxias (SСAs) are a highly heterogeneous group of inherited neurological disorders. The symptoms of ataxia vary in individual patients and even within the same SCA subtype. A study of a four-...
Jessica L Klein,Monica E Lemmon,Frances J Northington et al. Jessica L Klein et al.
Cerebellar abnormalities are encountered in a high number of neurological diseases that present in the neonatal period. These disorders can be categorized broadly as inherited (e.g. malformations, inborn errors of metabolism) or acquired (e...
Kim van Dun,Elke De Witte,Wendy Van Daele et al. Kim van Dun et al.
Background: In the majority of right-handed subjects, language processing is subserved by a close interplay between the left cerebral hemisphere and right cerebellum. Within this network, the dominant fronto-insular regio...