Merosin negative congenital muscular dystrophy diffusion weighted imaging findings of brain

Basit Öğe Kaydı
dc.authorid7768en_US
dc.contributor.authorAlkan, Alpay
dc.contributor.authorSığırcı, Ahmet
dc.contributor.authorKutlu, Ramazan
dc.contributor.authorAslan, Mehmet
dc.contributor.authorDoğanay, Selim
dc.contributor.authorYakıncı, Mehmet Cengiz
dc.date.accessioned2017-06-23T06:37:40Z
dc.date.available2017-06-23T06:37:40Z
dc.date.issued2007
dc.departmentİnönü Üniversitesien_US
dc.description.abstractMerosin-negative congenital muscular dystrophy is a rare genetic disease of childhood involving the central and peripheral nervous system. There were high signal intensities throughout the centrum semiovale, periventricular, and subcortical white matters on T2-weighted images in a 4-year-old girl with merosin-negative congenital muscular dystrophy. An apparent diffusion coefficient map revealed increased signal intensity and apparent diffusion coefficient values in the periventricular and deep white matters. It may be attributable to increased water content in the white matter because of an abnormal blood-brain barrier rather than to decreased or abnormal myelination.en_US
dc.identifier.citationAlkan, A. Sığırcı, A. Kutlu, R. Aslan, M. Doğanay, S. Yakıncı, M. C. (2007). Merosin negative congenital muscular dystrophy diffusion weighted imaging findings of brain. J Child Neurol, (22), 655–659.en_US
dc.identifier.endpage659en_US
dc.identifier.startpage655en_US
dc.identifier.urihttp://jcn.sagepub.com/content/22/5/655.long
dc.identifier.urihttps://hdl.handle.net/11616/7144
dc.identifier.volume22en_US
dc.language.isoenen_US
dc.publisherJ Child Neurolen_US
dc.relation.ispartofJ Child Neurolen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMuscular dystrophyen_US
dc.subjectMagnetic resonance imagingen_US
dc.titleMerosin negative congenital muscular dystrophy diffusion weighted imaging findings of brainen_US
dc.typeArticleen_US

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