16429376

Source:http://linkedlifedata.com/resource/pubmed/id/16429376

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0024485, umls-concept:C0086024, umls-concept:C1457869, umls-concept:C1833334, umls-concept:C2607943, umls-concept:C2926606
pubmed:issue	6
pubmed:dateCreated	2006-1-23
pubmed:abstractText	Cobalamin C/D defect is an inborn error of cobalamin metabolism causing methylmalonic aciduria and homocystinuria. The early-onset form is characterized by severe neurological impairment. The aim of this study was to evaluate and monitor brain damage in early-onset cbl-C/D defect by conventional MRI and to assess the additional value of 1H-MRS.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8101187
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0174-304X
pubmed:author	pubmed-author:BoenziSS, pubmed-author:CannatàVV, pubmed-author:DeodatoFF, pubmed-author:Dionisi-ViciCC, pubmed-author:FarielloGG, pubmed-author:GenoveseEE, pubmed-author:LongoDD
pubmed:issnType	Print
pubmed:volume	36
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	366-72
pubmed:dateRevised	2008-1-16
pubmed:meshHeading	pubmed-meshheading:16429376-Brain Diseases, Metabolic, Inborn, pubmed-meshheading:16429376-Humans, pubmed-meshheading:16429376-Infant, pubmed-meshheading:16429376-Infant, Newborn, pubmed-meshheading:16429376-Magnetic Resonance Imaging, pubmed-meshheading:16429376-Magnetic Resonance Spectroscopy, pubmed-meshheading:16429376-Vitamin B 12 Deficiency
pubmed:year	2005
pubmed:articleTitle	MRI and 1H-MRS findings in early-onset cobalamin C/D defect.
pubmed:affiliation	Department of Paediatric Radiology, Bambino Gesù Children's Hospital, Rome, Italy.
pubmed:publicationType	Journal Article, Comparative Study