Results 151 to 160 of about 114,557 (289)

The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene A história da ataxia espinocerebelar tipo 10 no Brasil: as viagens de um gene

Arquivos de Neuro-Psiquiatria, 2007
The authors report the history of spinocerebellar ataxia 10 (SCA10), since its first report in a large Portuguese-ancestry Family with autosomal dominant pure cerebellar ataxia, till the final identification of further families without Mexican ancestry ...
Hélio A.G. Teive, Walter O. Arruda, Salmo Raskin, Tetsuo Ashizawa, Lineu César Werneck   +4 more
doaj   +1 more source

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia [PDF]

, 2000
Jenni Jonasson, Vesa Juvonen, Pertti Sistonen, Jaakko Ignatius, Daniel Johansson, Erik Björck, Jan Wahlström, Atle Melberg, Gösta Holmgren, Lars Forsgren, Monica Holmberg   +10 more
openalex   +1 more source

Dystonia and Ataxia Associated with Brain Iron Accumulation: Expanding the Phenotype of NPTX1‐Spinocerebellar Ataxia 50

Movement Disorders, EarlyView.
Gianmarco Dalla Zanna, Alessandra Tessa, Salvatore Rossi, Antonio Funcis, Francesca Brambati, Anna Modoni, Rosellina Russo, Paolo Calabresi, Filippo Maria Santorelli, Gabriella Silvestri   +9 more
wiley   +1 more source

Sleep Related Movement Disorders: What's New and Changing Clinical Practice

Journal of Sleep Research, Volume 34, Issue 6, December 2025.
ABSTRACT Restless legs syndrome (RLS) is a common sensorimotor disorder, and the most common sleep‐related movement disorder with a prevalence of up to 15% in the European and US population. This review addresses key aspects of RLS, focusing on novel data that have or will likely have an impact on clinical practice.
Ambra Stefani, Qi Tang, Stefan Clemens, Lourdes M. DelRosso, Diego Garcia‐Borreguero, Raffaele Ferri, Birgit Frauscher, Evi Holzknecht, Federica Provini, Barbara Schormair, John Winkelman, Birgit Högl   +11 more
wiley   +1 more source

Spinocerebellar Ataxia 21 with Retardation

Pediatric Neurology Briefs, 2014
Investigators at Universite de Lille Nord de France, and other centers in France, report the identification of a novel causative gene for spinocerebellar ataxia 21, an autosomal dominant disorder, initially mapped to chromosome 7 and designated as SCA21.
J Gordon Millichap, John J Millichap
doaj   +1 more source

A refractory head tremor appearing after volatile anesthesia combined with epidural anesthesia in a patient with spinocerebellar ataxia type 6 [PDF]

, 2018
Takaya Nishida, Masayori Nakajima
openalex   +1 more source

The “Hot Cross Bun Sign” in Spinocerebellar Ataxia Types 2 and 7–Case Reports and Review of Literature

, 2022
Ansuya Kasavelu Naidoo, Cait‐Lynn Deanne Wells, Yashvir Rugbeer, Neil Naidoo   +3 more
openalex   +1 more source

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy

Brain : a journal of neurology, 2018
Higuchi et al. identify recessive mutations in the mitochondrial gene, cytochrome c oxidase assembly factor 7 (COA7) in four unrelated patients with an axonal-type motor and sensory neuropathy with ataxia.
Y. Higuchi, Ryuta Okunushi, Taichi Hara, A. Hashiguchi, Junhui Yuan, A. Yoshimura, K. Murayama, A. Ohtake, M. Ando, Y. Hiramatsu, S. Ishihara, H. Tanabe, Y. Okamoto, E. Matsuura, Takehiro Ueda, T. Toda, S. Yamashita, Kenichiro Yamada, T. Koide, H. Yaguchi, J. Mitsui, H. Ishiura, J. Yoshimura, K. Doi, S. Morishita, Ken Sato, M. Nakagawa, M. Yamaguchi, S. Tsuji, H. Takashima   +29 more
semanticscholar   +1 more source

Phase‐Specific Contributions and Interactions of the Left and Right Posterior Middle Temporal Gyri in Vocal Feedback Control: Evidence From Dual‐Site TMS

Human Brain Mapping, Volume 46, Issue 16, November 2025.
This study demonstrates the causal roles of the left and right posterior middle temporal gyri in vocal feedback control and reveals a phase‐specific interhemispheric mechanism that transitions from coordinated error detection to independent correction, offering novel neuromodulation strategies for speech rehabilitation.
Qingqing Liu, Jiating Li, Shuzhi Zhao, Mingyun Chen, Xin Huang, Dongxu Liu, Jingting Li, Xiuqin Wu, Yongxue Li, Xi Chen, Peng Liu, Guangyan Dai, Hanjun Liu   +12 more
wiley   +1 more source

Intensive Outpatient Treatment of Depression in a Spinocerebellar Ataxia Type 1 Patient

Case Reports in Psychiatry, 2019
Objective. Spinocerebellar ataxia type 1 (SCA1) is but one subtype of spinocerebellar ataxia (SCA), each of which can possibly be considered a separate neurological condition (N. Whaley, S. Fujioka, Z. K. Wszolek, 2011).
Eric Black
doaj   +1 more source