Hirayama Disease (monomelic amyotrophy)
| dc.contributor.author | Alkan, Gökhan | |
| dc.contributor.author | Akgöl, Gürkan | |
| dc.contributor.author | Gülkesen, Arif | |
| dc.contributor.author | Kaya, Arzu | |
| dc.date.accessioned | 2026-08-12T15:55:20Z | |
| dc.date.issued | 2017 | |
| dc.department | Fırat Üniversitesi | |
| dc.description.abstract | Hirayama disease (HD) or monomelic amyotrophy (MA) is a rare muscular atrophy that affects young Asian males, usually occurs in one of the upper limbs that progresses slowly. It is diagnosed by means of electromyographic/electroneurographic conduction speed studies and by magnetic resonance imaging (MRI) of the spinal cord. In this paper two different HD case is reported | |
| dc.identifier.endpage | 561 | |
| dc.identifier.issn | 2147-0634 | |
| dc.identifier.issue | 3 | |
| dc.identifier.startpage | 560 | |
| dc.identifier.trdizinid | 264279 | |
| dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/264279 | |
| dc.identifier.uri | https://hdl.handle.net/11508/39158 | |
| dc.identifier.volume | 6 | |
| dc.indekslendigikaynak | TR-Dizin | |
| dc.language.iso | en | |
| dc.relation.ispartof | Medicine Science | |
| dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.relation.tubitak | info:eu-repo/grantAgreement/TUBITAK// | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_TR-Dizin_20260511 | |
| dc.subject | Genel ve Dahili Tıp | |
| dc.subject | Nörolojik Bilimler | |
| dc.title | Hirayama Disease (monomelic amyotrophy) | |
| dc.type | Article |
