9951005

Source:http://linkedlifedata.com/resource/pubmed/id/9951005

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0220825, umls-concept:C0752121
pubmed:issue	160
pubmed:dateCreated	1999-4-29
pubmed:abstractText	Type 2 spinocerebellar ataxia (SCA2) is the condition most often described (to date) in patients with hereditary ataxia, its prevalence being 52 per 100,000 persons.
pubmed:language	spa
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7706841
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0210-0010
pubmed:author	pubmed-author:MedinaE EEE, pubmed-author:VelázquezLL
pubmed:issnType	Print
pubmed:volume	27
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	921-6
pubmed:dateRevised	2009-5-28
pubmed:meshHeading	pubmed-meshheading:9951005-Adolescent, pubmed-meshheading:9951005-Adult, pubmed-meshheading:9951005-Aged, pubmed-meshheading:9951005-Cross-Sectional Studies, pubmed-meshheading:9951005-Electromyography, pubmed-meshheading:9951005-Female, pubmed-meshheading:9951005-H-Reflex, pubmed-meshheading:9951005-Humans, pubmed-meshheading:9951005-Male, pubmed-meshheading:9951005-Middle Aged, pubmed-meshheading:9951005-Motor Neurons, pubmed-meshheading:9951005-Neural Conduction, pubmed-meshheading:9951005-Peripheral Nerves, pubmed-meshheading:9951005-Spinocerebellar Degenerations
pubmed:year	1998
pubmed:articleTitle	[Neurophysiological evaluation of patients with spinocerebellar ataxia type 2].
pubmed:affiliation	Laboratorio de Neurofisiología Clínica, Hospital Docente Provincial Vladimir Ilich Lenin, Holguín, Cuba.
pubmed:publicationType	Journal Article, English Abstract