Results 11 to 20 of about 101,774 (257)

Cerebellar development and disease [PDF]

Current Opinion in Neurobiology, 2008
The molecular control of cell-type specification within the developing cerebellum as well as the genetic causes of the most common human developmental cerebellar disorders have long remained mysterious. Recent genetic lineage and loss-of-function data from mice have revealed unique and nonoverlapping anatomical origins for GABAergic neurons from ...
Kathleen J, Millen, Joseph G, Gleeson
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Phenotypic and genetic aspects of hereditary ataxia in dogs

Journal of Veterinary Internal Medicine, 2023
Hereditary ataxias are a large group of neurodegenerative diseases that have cerebellar or spinocerebellar dysfunction as core feature, occurring as an isolated sign or as part of a syndrome.
Kimberley Stee, Mario Van Poucke, Mark Lowrie, Luc Van Ham, Luc Peelman, Natasha Olby, Sofie F.M. Bhatti   +6 more
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A Classical Sign with Uncommon Symptoms: Joubert Syndrome Presenting with Retinal Dystrophy and Keratoconus [PDF]

Journal of Clinical and Diagnostic Research
Joubert Syndrome and Related Disorders (JSRD) are a rare group of autosomal recessive ciliopathies characterised by the pathognomonic molar-tooth sign on Magnetic Resonance Imaging (MRI) of the brain. The clinical manifestations are usually multisystemic
Yeddula Pranay Raja, Shivam Gupta, Anupama K George, N Kamala, Nirmala Devi Chandrasekaran5   +4 more
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Cerebellar Syndromes: A Medical Student Guide

International Journal of Medical Students, 2013
The cerebellum is central to normal motor function and co-ordination, and can be frequently affected in a number of common disease processes. However, medical student teaching relating to cerebellar anatomy and pathology is lacking, leaving many ...
Claudia K. Sellers, Suvankar Pal
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Cerebellar connectome alterations and associated genetic signatures in multiple sclerosis and neuromyelitis optica spectrum disorder

Journal of Translational Medicine, 2023
Background The cerebellum plays key roles in the pathology of multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD), but the way in which these conditions affect how the cerebellum communicates with the rest of the brain (its ...
Yuping Yang, Junle Li, Ting Li, Zhen Li, Zhizheng Zhuo, Xuemei Han, Yunyun Duan, Guanmei Cao, Fenglian Zheng, Decai Tian, Xinli Wang, Xinghu Zhang, Kuncheng Li, Fuqing Zhou, Muhua Huang, Yuxin Li, Haiqing Li, Yongmei Li, Chun Zeng, Ningnannan Zhang, Jie Sun, Chunshui Yu, Fudong Shi, Umer Asgher, Nils Muhlert, Yaou Liu, Jinhui Wang   +26 more
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SYMPTOMATOLOGY OF CEREBELLAR DISEASE [PDF]

The American Journal of the Medical Sciences, 1895
n ...
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Ataxias cerebelares hereditárias: do martelo ao gen Hereditary cerebellar ataxias from neurological hammer to genetics

Arquivos de Neuro-Psiquiatria, 1997
As heredoataxias constituem grupo complexo de doenças neurodegenerativas hereditárias, para o qual várias formas de classificação clínica e patológica foram propostas com sucesso variável.
Walter Oleschko Arruda, Hélio A. Ghizoni Teive   +1 more
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Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement

Frontiers in Neurology, 2022
Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders clinically characterized by progressive lower-limb spasticity. Cerebellar ataxia commonly co-occurs with complicated HSPs.
Min-Yu Lan, Min-Yu Lan, Min-Yu Lan, Chin-Song Lu, Chin-Song Lu, Shey-Lin Wu, Shey-Lin Wu, Ying-Fa Chen, Ying-Fa Chen, Yueh-Feng Sung, Min-Chien Tu, Min-Chien Tu, Yung-Yee Chang, Yung-Yee Chang   +13 more
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CEREBELLAR DISEASES [PDF]

The Journal of Nervous and Mental Disease, 1879
n ...
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Slow saccades in cerebellar disease [PDF]

Cerebellum & Ataxias, 2019
Eye movements are frequently considered diagnostic markers indicating involvement of the cerebellum. Impaired amplitude of saccades (saccade dysmetria), impaired gaze holding function (horizontal or downbeat nystagmus), and interrupted (choppy) pursuit are typically considered hallmarks of cerebellar disorders.
Jensen, Kelsey, Beylergil, Sinem Balta, Shaikh, Aasef G.   +2 more
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