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dc.contributor.authorCALISKAN, M
dc.contributor.authorAPAK, S
dc.contributor.authorGOEBEL, HH
dc.contributor.authorOZMEN, M
dc.date.accessioned2021-03-03T13:06:55Z
dc.date.available2021-03-03T13:06:55Z
dc.date.issued1991
dc.identifier.citationOZMEN M., CALISKAN M., GOEBEL H., APAK S., "INFANTILE NEUROAXONAL DYSTROPHY - DIAGNOSIS BY SKIN BIOPSY", BRAIN & DEVELOPMENT, cilt.13, sa.4, ss.256-259, 1991
dc.identifier.issn0387-7604
dc.identifier.otherav_3215dfa5-6c8f-415e-bb3e-f1751564d257
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/38028
dc.identifier.urihttps://doi.org/10.1016/s0387-7604(12)80059-3
dc.description.abstractA child who shows progressive motor and mental deterioration after the first year of life, who has pyramidal signs, marked muscle hypotonia, but no seizures, suggests to have infantile neuroaxonal dystrophy (INAD). Beyond the age of two years, the EEG also entails characteristic findings. Diagnosis may be obtained by an ultrastructural examination of biopsied skin. The respective clinical and morphological findings are recorded and illustrated from four patients in this report.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleINFANTILE NEUROAXONAL DYSTROPHY - DIAGNOSIS BY SKIN BIOPSY
dc.typeMakale
dc.relation.journalBRAIN & DEVELOPMENT
dc.contributor.department, ,
dc.identifier.volume13
dc.identifier.issue4
dc.identifier.startpage256
dc.identifier.endpage259
dc.contributor.firstauthorID112819


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