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Autor:
Mirjeta Hasani, Ivana Božinovikj, Aleksandra Kolevska, Erieta Nikolikj Dimitrova, Simona Ristovska, Aleksandra Hadzieva Pejcikj
Publikováno v:
Open Access Macedonian Journal of Medical Sciences; Vol 4, No 3 (2016): Sep 15 (OAMJMS); 443-448
Open Access Macedonian Journal of Medical Sciences; Vol. 4 No. 3 (2016): Sep 15 (OAMJMS); 443-448
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences, Vol 4, Iss 3, Pp 443-448 (2016)
Open Access Macedonian Journal of Medical Sciences; Vol. 4 No. 3 (2016): Sep 15 (OAMJMS); 443-448
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences, Vol 4, Iss 3, Pp 443-448 (2016)
BACKGROUND: Charcot-Marie-Tooth (CMT) disease is a hereditary disease with signs of chronic non-progressive motor-sensory neuropathy which is characterised by symmetric muscle atrophy and weakness of the distal portion of lower extremities.AIM: The a