期 |
栏目 |
标题 |
文件 |
卷 1, 编号 1 (2007) |
Original articles |
Heterogeneity of sporadic Parkinson’s disease: molecular approach to solving the problem |
(Rus)
|
卷 1, 编号 2 (2007) |
Original articles |
Familial case of ataxia with oculomotor apraxia: first observation in Russian population |
(Rus)
|
卷 1, 编号 4 (2007) |
Original articles |
Congenital pathological tortuosity of the internal carotid artery: population screening and genetic aspects |
(Rus)
|
卷 1, 编号 4 (2007) |
Original articles |
Voxel-guided morphometry: a new method for assessment of local secondary atrophic changes of the brain |
(Rus)
|
卷 2, 编号 2 (2008) |
Original articles |
Perspectives of nanotechnologies in clinical neurology |
(Rus)
|
卷 2, 编号 2 (2008) |
Original articles |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): first description of a Russian family with the identified mutation in the Notch3 gene |
(Rus)
|
卷 4, 编号 4 (2010) |
Original articles |
Possibilities of transcranial sonography in extrapyramidal disorders |
(Rus)
|
卷 5, 编号 4 (2011) |
Original articles |
Recurrent facial nerve neuropathies: clinical, electrophysiological and molecular analysis |
(Rus)
|
卷 5, 编号 4 (2011) |
Original articles |
Induced pluripotent stem cells: new possibilities in neurobiology and neurotransplantaion |
(Rus)
|