9541317

Source:http://linkedlifedata.com/resource/pubmed/id/9541317

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0021270, umls-concept:C0043116, umls-concept:C2607943, umls-concept:C2926606
pubmed:issue	3
pubmed:dateCreated	1998-5-21
pubmed:abstractText	We report two infants with Werdnig-Hoffmann disease diagnosed by means of spinal MR imaging, histopathologic examination of muscle biopsy specimens, cloned DNA analysis, electrophysiological examination, and clinical history. The MR findings were consistent with previous histopathologic reports.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8003708
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0195-6108
pubmed:author	pubmed-author:ChenC YCY, pubmed-author:ChenY HYH, pubmed-author:HsuC FCF, pubmed-author:HsuY TYT, pubmed-author:LucM MMM, pubmed-author:ZimmermanR ARA
pubmed:issnType	Print
pubmed:volume	19
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	550-2
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:9541317-Atrophy, pubmed-meshheading:9541317-Electromyography, pubmed-meshheading:9541317-Electrophysiology, pubmed-meshheading:9541317-Female, pubmed-meshheading:9541317-Gene Deletion, pubmed-meshheading:9541317-Humans, pubmed-meshheading:9541317-Infant, pubmed-meshheading:9541317-Magnetic Resonance Imaging, pubmed-meshheading:9541317-Male, pubmed-meshheading:9541317-Muscle, Skeletal, pubmed-meshheading:9541317-Muscle Fibers, Skeletal, pubmed-meshheading:9541317-Spinal Muscular Atrophies of Childhood
pubmed:year	1998
pubmed:articleTitle	MR findings of Werdnig-Hoffmann disease in two infants.
pubmed:affiliation	Department of Pediatrics, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.
pubmed:publicationType	Journal Article, Case Reports