17434771

Source:http://linkedlifedata.com/resource/pubmed/id/17434771

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007320, umls-concept:C0015219, umls-concept:C0085973, umls-concept:C0205494, umls-concept:C0282441, umls-concept:C0342773
pubmed:issue	4
pubmed:dateCreated	2007-6-5
pubmed:abstractText	Pearson syndrome (PS) is an uncommon specific syndrome among mitochondrial diseases. It has unique clinical presentations.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9715169
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1090-3798
pubmed:author	pubmed-author:ChangTe-KauTK, pubmed-author:ChiChing-ShiangCS, pubmed-author:LeeHsiu-FenHF, pubmed-author:LeeHuei-JaneHJ, pubmed-author:TsaiChi-RenCR, pubmed-author:WangChau-JongCJ
pubmed:issnType	Print
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	208-14
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:17434771-Base Sequence, pubmed-meshheading:17434771-Brain, pubmed-meshheading:17434771-Child, Preschool, pubmed-meshheading:17434771-Chromosome Deletion, pubmed-meshheading:17434771-DNA, Mitochondrial, pubmed-meshheading:17434771-DNA Mutational Analysis, pubmed-meshheading:17434771-Female, pubmed-meshheading:17434771-Humans, pubmed-meshheading:17434771-Infant, pubmed-meshheading:17434771-Infant, Newborn, pubmed-meshheading:17434771-Kearns-Sayre Syndrome, pubmed-meshheading:17434771-Leigh Disease, pubmed-meshheading:17434771-Magnetic Resonance Imaging, pubmed-meshheading:17434771-Mitochondrial Diseases, pubmed-meshheading:17434771-Molecular Sequence Data, pubmed-meshheading:17434771-Polymerase Chain Reaction
pubmed:year	2007
pubmed:articleTitle	The neurological evolution of Pearson syndrome: case report and literature review.
pubmed:affiliation	Department of Pediatrics, Taichung Veterans General Hospital, No. 160, Sec. 3 Taichung-Kang Road, Taichung 407, Taiwan, ROC.
pubmed:publicationType	Journal Article, Case Reports