| dc.contributor.author | TOPALOGLU, H | |
| dc.contributor.author | YALAZ, K | |
| dc.contributor.author | RENDA, Y | |
| dc.contributor.author | CAGLAR, M | |
| dc.contributor.author | GOGUS, S | |
| dc.contributor.author | KALE, G | |
| dc.contributor.author | GUCUYENER, K | |
| dc.contributor.author | NURLU, G | |
| dc.date.accessioned | 2019-12-10T10:50:00Z | |
| dc.date.available | 2019-12-10T10:50:00Z | |
| dc.date.issued | 1991 | |
| dc.identifier.issn | 0022-3050 | |
| dc.identifier.uri | https://doi.org/10.1136/jnnp.54.3.226 | |
| dc.identifier.uri | http://hdl.handle.net/11655/14287 | |
| dc.description.abstract | Occidental type cerebromuscular dystrophy (OCMD) forms a substantial distinct group within congenital muscular dystrophy (CMD). These patients invariably present with amyotrophy, multiple joint contractures, facial muscle involvement, normal or nearly normal intelligence, leukodystrophic appearance on CT scan, and dystrophic changes in muscle. | |
| dc.language.iso | en | |
| dc.publisher | British Med Journal Publ Group | |
| dc.relation.isversionof | 10.1136/jnnp.54.3.226 | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Neurosciences & Neurology | |
| dc.subject | Psychiatry | |
| dc.subject | Surgery | |
| dc.title | Occidental Type Cerebromuscular Dystrophy - A Report Of 11 Cases | |
| dc.type | info:eu-repo/semantics/article | |
| dc.relation.journal | Journal Of Neurology Neurosurgery And Psychiatry | |
| dc.contributor.department | Çocuk Sağlığı ve Hastalıkları | |
| dc.identifier.volume | 54 | |
| dc.identifier.issue | 3 | |
| dc.identifier.startpage | 226 | |
| dc.identifier.endpage | 229 | |
| dc.description.index | WoS | |
| dc.description.index | Scopus | |
