نتایج جستجو برای: s ataxia

تعداد نتایج: 727569  

Journal: :Neuro endocrinology letters 2005
Alena Zumrová Radim Mazanec Martin Vyhnálek Anna Krepelová Zuzana Musová Stefanie Krilová Ludmila Appltová Markéta Havlovicová

DNA testing broadens diagnostic tools available for hereditary ataxias. However, together with current knowledge of genes and their mutations crop up new phenotype figures of diseases already well known. Diagnostic problems in practice can consist in part due to the very similar symptoms of hereditary ataxias and acquaintance in or availability of new techniques such as DNA testing and result i...

Journal: :The Journal of Nervous and Mental Disease 1892

2010
Wafaa M. Farghaly Hamdy N. El-Tallawy Tarek A. Rageh Ghaydaa A. Shehata Nabil A. Metwally Noha M. Abo-Elfetoh

Background: Rare comprehensive epidemiological studies of ataxia have been undertaken worldwide. Objective: To estimate the prevalence of cerebellar ataxia and its subtypes in Al-Kharga District New Valley. Methods: This is a community based study carried out through three stages. Total populations 62,583 were screened door to door (every door) by three specialists of neurology. All suspected p...

Journal: :Physical therapy 1997
A J Bastian

Ataxia, or incoordination of movement, is a disorder that can be caused by damage to several different nervous system structures. Common causes of ataxia include damage of the cerebellum and damage of sensory structures. Sensory ataxia is distinguishable from cerebellar ataxia, because the sensory ataxia causes symptoms to worsen when movements are made with the eyes closed. The basic mechanism...

Journal: :Pediatric Neurology Briefs 1988

Journal: :Journal of Child Neurology 2012

Journal: :Proceedings of the Royal Society of Medicine 1911

Journal: :Stroke 2011

Journal: :Blood 2005
Ian Napier Prem Ponka Des R Richardson

It is well known that iron (Fe) is transported to the mitochondrion for heme synthesis. However, only recently has the importance of this organelle for many other facets of Fe metabolism become widely appreciated. Indeed, this was stimulated by the description of human disease states that implicate mitochondrial Fe metabolism. In particular, studies assessing various diseases leading to mitocho...

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 ...

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