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Genetic genealogy / Medical genetics / Channelopathy / Rare diseases / Spinocerebellar ataxia / Machado–Joseph disease / Dentatorubral-pallidoluysian atrophy / Ataxia / ATXN2 / Health / Neurodegenerative disorders / Neurological disorders


Clinical significance of serological biomarkers and neuropsychological performances in patients with temporal lobe epilepsy
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City

Santos / Mean / Bangkok / Ratchaburi / Buriram / Santiago / Nagano / Lyon / Davis / Wadia / Rouleau / Chiba / Horn / Nicholson / Lee / /

Company

Lang AE / SCA2 / SCA1 / SCA6 / SCA7 / Neurogenetic Fund / Robb SA / QIAGEN / Ranum LP / Stata Corp. College / Wiwat Raksriaksorn Fund / TaKaRa / MJD / Google / Harding AE / Beckman Coulter / Walworth / HP / Creative Commons / BioMed Central Ltd. / Shimizu / /

Country

Thailand / Japan / Korea / United States / Singapore / /

Currency

pence / /

/

Facility

Buriram Hospital / Ratchaburi Hospital / Ramathibodi Hospital / College Station / Mahidol University / Chiang Mai University / Bhumibol Adulyadej Hospital / /

IndustryTerm

familial / /

MedicalCondition

dysarthria / dementia / common spinocerebellar ataxias / retinitis pigmentosa / Ophthalmoplegia Background Spinocerebellar ataxias / vertical nystagmus / macular degeneration / dominant cerebellar ataxia / chorea / spinocerebellar ataxia type 1 / spinocerebellar ataxia 2 / polyneuropathy / spinocerebellar ataxia type 2 / cerebellar ataxias / genetically heterogeneous neurodegenerative disorders / ataxias / paresis / spinocerebellar ataxia 7 / Spinocerebellar ataxia 3 / Gait ataxia / autoimmune cerebellar disorders / hereditary / hyperreflexia / Truncal ataxia / parkinsonism / commonly episodic ataxia / MJD Machado-Joseph disease / Horizontal nystagmus / cognitive impairment / ophthalmoplegia / extrapyramidal features / multiple system atrophy / Machado-Joseph disease / Movement disorders / diseases / dystonia / disorders / Spinocerebellar ataxia / spastic / Optic atrophy / Thai ataxia families / spinocerebellar ataxia type 6 / SCA spinocerebellar ataxia / fasciculation / facial fasciculation / adult-onset spinocerebellar ataxias / peripheral neuropathy / spinocerebellar ataxia type 3 / progressive ataxia / Limb ataxia / progressive cerebellar ataxia / MS / ataxia / cerebellar ataxia / Brain pathology / ophthalmoparesis / disease / dominantly inherited spinocerebellar ataxias / familial spinocerebellar ataxias / spinocerebellar ataxias / dentatorubral pallidoluysian atrophy / azoospermia / /

Organization

Chiang Mai University / Department of Medicine / Division of Neurology / Human Genome Nomenclature Committee / Faculty of Medicine / Ramathibodi Hospital / Mahidol University / Bangkok / /

Person

Ann Neurol / Supoch Tunlayadechanont / Arch Neurol / Maurice M. Broughton / Chonticha Prasartsakulchai / Siwaporn Chankrachang / Manisa Busabaratana / Natsharee Pulkes / Martinez Rodriguez / Jesada Keandoungchun / Aruchalean Taweewongsounton / Ann N Y Acad Sci / /

Position

author / Major / forward / investigator / HB / Walker / WB / Fisher / /

ProvinceOrState

Alaska / Phayao / Georgia / Wyoming / Manitoba / Pennsylvania / New Hampshire / /

Region

eastern India / /

Technology

research protocol / Human Genome / genotype / alpha / /

URL

http /

SocialTag