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dc.contributor.authorJ Gordon Millichap
dc.contributor.otherNorthwestern University Feinberg School of Medicine
dc.date.accessioned2016-03-14T05:00:58Z
dc.date.available2025-10-02T03:46:46Z
dc.date.issued01-03-2006
dc.identifier.issn-
dc.identifier.urihttps://www.pediatricneurologybriefs.com/articles/1176
dc.description.abstractBrain magnetic resonance imaging (MRI) findings in 13 patients with congenital muscular dystrophy (MDCIC) and Fukutin-related protein (FKRP) gene mutations were retrospectively reviewed in a study at Hammersmith Hospital, London, UK, and European centers.
dc.format-
dc.language.isoEN
dc.publisherPediatric Neurology Briefs Publishers
dc.relation.uri['http://revistas.uned.es/index.php/ETFIV/about/editorialPolicies#focusAndScope', 'http://revistas.uned.es/index.php/ETFIV', 'http://revistas.uned.es/index.php/ETFIV/about/submissions#authorGuidelines']
dc.rightsCC BY-NC
dc.subject['history', 'early modern history', 'historiography', 'History (General) and history of Europe', 'D', 'History (General)', 'D1-2009', 'Modern history, 1453-', 'D204-475']
dc.subject.lccPediatrics
dc.titleBrain MRI Findings in Congenital Muscular Dystrophy
dc.typeArticle
dc.description.keywordscongenital muscular dystrophy
dc.description.keywordswalker-warburg syndrome
dc.description.keywordsbrain magnetic resonance imaging
dc.description.pages22-22
dc.description.doi10.15844/pedneurbriefs-20-3-7
dc.title.journalPediatric Neurology Briefs
dc.identifier.e-issn2166-6482
dc.identifier.oaioai:doaj.org/journal:1112c96f27544f58abe03689226ba1f8
dc.journal.infoVolume 20, Issue 3


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