12172062

Source:http://linkedlifedata.com/resource/pubmed/id/12172062

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007320, umls-concept:C0035304, umls-concept:C0085973, umls-concept:C0752125
pubmed:issue	4
pubmed:dateCreated	2002-8-12
pubmed:abstractText	A 60-yr-old man developed progressive gait disturbance and limb ataxia at the age of 52. Family history was absent for neurological disorders. Examinations showed pure cerebellar syndrome. There was no retinal degeneration for 7 yr. A brain MRI done at the age of 56 showed atrophy of the cerebellar hemispheres and vermis. Genetic test confirmed the spinocerebellar ataxia type 7 with CAG repeat number of 42.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8703518
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1011-8934
pubmed:author	pubmed-author:ChoKi-HyunKH, pubmed-author:JeonBeom SBS, pubmed-author:KimByeong-ChaeBC, pubmed-author:KimMyeong-KyuMK
pubmed:issnType	Print
pubmed:volume	17
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	577-9
pubmed:dateRevised	2011-3-16
pubmed:meshHeading	pubmed-meshheading:12172062-Brain, pubmed-meshheading:12172062-Humans, pubmed-meshheading:12172062-Korea, pubmed-meshheading:12172062-Magnetic Resonance Imaging, pubmed-meshheading:12172062-Male, pubmed-meshheading:12172062-Middle Aged, pubmed-meshheading:12172062-Retinal Degeneration, pubmed-meshheading:12172062-Spinocerebellar Ataxias, pubmed-meshheading:12172062-Trinucleotide Repeat Expansion
pubmed:year	2002
pubmed:articleTitle	Spinocerebellar ataxia type 7 without retinal degeneration: a case report.
pubmed:affiliation	Department of Neurology, Chonnam National University Medical School, Gwangju, Korea.
pubmed:publicationType	Journal Article, Case Reports