نتایج جستجو برای: cerebellar

تعداد نتایج: 26465  

Journal: :Proceedings of the Royal Society of Medicine 1911

Journal: :Neurologia medico-chirurgica 1987

Journal: :Nature Reviews Neuroscience 2003

Journal: :Neurology 2007
Elan D Louis Wei Zheng Xiangling Mao Dikoma C Shungu

BACKGROUND On proton magnetic resonance spectroscopic imaging ((1)H MRSI), there is a decrease in cerebellar N-acetylaspartate/total creatine (NAA/tCr) in essential tremor (ET), signifying cerebellar neuronal dysfunction or degeneration. Harmane, which is present in the human diet, is a potent tremor-producing neurotoxin. Blood harmane concentrations seem to be elevated in ET. OBJECTIVES To a...

2017
Ryuji Sakakibara Fuyuki Tateno Masahiko Kishi Yohei Tsuyusaki Yosuke Aiba Hitoshi Terada Tsutomu Inaoka Setsu Sawai Satoshi Kuwabara Fumio Nomura

OBJECTIVE Diagnosis of sporadic cerebellar ataxia is a challenge for neurologists. A wide range of potential causes exist, including chronic alcohol use, multiple system atrophy of cerebellar type (MSA-C), and sporadic late cortical cerebellar atrophy. Recently, an autosomal-dominant spinocerebellar ataxia (SCA) mutation was identified in a cohort of patients with non-MSA-C sporadic cerebellar ...

Journal: :Neurology 2021

Objectives Gay matter (GM) involvement is clinically relevant in multiple sclerosis (MS). Using source-based morphometry (SBM), we characterized GM atrophy and its 1-year evolution across different MS phenotypes. Methods Clinical MRI data were obtained at 8 European sites from 170 healthy controls (HCs) 398 patients with (34 isolated syndrome [CIS], 226 relapsing-remitting [RRMS], 95 secondary ...

Journal: :Brain : a journal of neurology 2015
Maria R Stefanescu Moritz Dohnalek Stefan Maderwald Markus Thürling Martina Minnerop Andreas Beck Marc Schlamann Joern Diedrichsen Mark E Ladd Dagmar Timmann

Spinocerebellar ataxia type 3, spinocerebellar ataxia type 6 and Friedreich's ataxia are common hereditary ataxias. Different patterns of atrophy of the cerebellar cortex are well known. Data on cerebellar nuclei are sparse. Whereas cerebellar nuclei have long been thought to be preserved in spinocerebellar ataxia type 6, histology shows marked atrophy of the nuclei in Friedreich's ataxia and s...

2017
Danielle E Whittaker Sahrunizam Kasah Alex P A Donovan Jacob Ellegood Kimberley L H Riegman Holger A Volk Imelda McGonnell Jason P Lerch M Albert Basson

Mutations in the gene encoding the ATP dependent chromatin-remodeling factor, CHD7 are the major cause of CHARGE (Coloboma, Heart defects, Atresia of the choanae, Retarded growth and development, Genital-urinary anomalies, and Ear defects) syndrome. Neurodevelopmental defects and a range of neurological signs have been identified in individuals with CHARGE syndrome, including developmental dela...

Journal: :Parkinsonism & related disorders 2012
Livia Brusa Roberto Ceravolo Lorenzo Kiferle Fabrizia Monteleone Cesare Iani Orazio Schillaci Paolo Stanzione Giacomo Koch

BACKGROUND Cerebellar repetitive transcranial magnetic stimulation may be effective in reducing peak-dose levodopa induced dyskinesia in Parkinson's disease patients. It was proposed that the antidyskinetic effect could be due to modulation of cerebello-thalamo-cortical pathways. However the neural basis for these clinical effects have not yet been demonstrated. METHODS We investigated the ef...

2013
Lucy A. Heap Chi Ching Goh Karin S. Kassahn Ethan K. Scott

The cerebellum is a brain region responsible for motor coordination and for refining motor programs. While a great deal is known about the structure and connectivity of the mammalian cerebellum, fundamental questions regarding its function in behavior remain unanswered. Recently, the zebrafish has emerged as a useful model organism for cerebellar studies, owing in part to the similarity in cere...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید