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dc.contributor.authorGunduz, E
dc.contributor.authorYalcinkaya, Cengiz
dc.contributor.authorSeven, Mehmet
dc.contributor.authorIslak, Civan
dc.contributor.authorYuksel, A
dc.date.accessioned2021-03-05T08:34:28Z
dc.date.available2021-03-05T08:34:28Z
dc.date.issued1999
dc.identifier.citationYuksel A., Yalcinkaya C., Islak C., Gunduz E., Seven M., "Neuroimaging findings of four patients with Sandhoff disease", PEDIATRIC NEUROLOGY, cilt.21, ss.562-565, 1999
dc.identifier.issn0887-8994
dc.identifier.otherav_9995a9e6-746f-4a54-b5d0-0a066148fed5
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/103285
dc.identifier.urihttps://doi.org/10.1016/s0887-8994(99)00041-7
dc.description.abstractSandhoff disease is a severe form of GM, gangliosidosis that is caused by the deficiency of both hexosaminidase A and B, Startle reaction, hypotonia, psychomotor retardation, and blindness are the main clinical features. Presented are computed tomography and magnetic resonance imaging findings of four patients with Sandhoff disease diagnosed by enzymatic analyses, Bilateral homogeneous thalamic hyperdensity was evident on computed tomography, Magnetic resonance imaging scans revealed mild cortical atrophy, a thin corpus callosum, and abnormal signal intensities in the caudate nucleus, globus pallidum, putamen, cerebellum, and brainstem, No correlation was evident between the severity of the central nervous system imaging findings and the clinical pictures. In this article the neuroimaging findings of four patients with Sandhoff disease are discussed, (C) 1999 by Elsevier Science Inc. All rights reserved.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleNeuroimaging findings of four patients with Sandhoff disease
dc.typeMakale
dc.relation.journalPEDIATRIC NEUROLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume21
dc.identifier.issue2
dc.identifier.startpage562
dc.identifier.endpage565
dc.contributor.firstauthorID14895


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