| Issue |
Section |
Title |
File |
| Vol 7, No 3 (2017) |
ORIGINAL REPORTS |
Clinical and genetic characteristics of autosomal recessive axonal neuropathy with neuromyotonia in Russian patients |
(Rus)
|
| Vol 7, No 3 (2017) |
CLINICAL DISCUSSION |
Bickerstaff brainstem encephalitis, acute transverse myelitis, and acute motor axonal neuropathy: diagnostic and treatment challenges in patients with concomitant syndromes. Clinical observation |
(Rus)
|
| Vol 7, No 4 (2017) |
LECTURES AND REVIEWS |
Thoracic outlet syndrome: clinical and diagnostic features |
(Rus)
|
| Vol 8, No 2 (2018) |
CLINICAL DISCUSSION |
A case of hereditary motor and sensory neuropathy type IVA with unusual genealogy |
(Rus)
|
| Vol 9, No 1 (2019) |
LECTURES AND REVIEWS |
Conduction block as an electrophysiological phenomenon: a review of the literature |
(Rus)
|
| Vol 9, No 3 (2019) |
CLINICAL DISCUSSION |
Clinical and genetic characteristics of Nonaka myopathy (GNE-myopathy) in russian patients |
(Rus)
|
| Vol 10, No 2 (2020) |
ORIGINAL REPORTS |
Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia |
(Rus)
|
| Vol 11, No 1 (2021) |
ORIGINAL REPORTS |
Diversity of VCP-related phenotypes: case report and literature review |
(Rus)
|
| Vol 11, No 4 (2021) |
CLINICAL DISCUSSION |
POLR3A-related hypomyelinating leukodystrophy: case report and literature review |
(Rus)
|
| Vol 12, No 2 (2022) |
ORIGINAL REPORTS |
Proximal spinal muscular atrophy 5q in the Republic of North Ossetia – Alania: population-genetic features, diagnostic problems and treatment prospects |
(Rus)
|
| Vol 12, No 4 (2022) |
CLINICAL DISCUSSION |
Reasons for misdiagnosis of polymyositis in patients with dysferlinopathy: a clinical case |
(Rus)
|
| Vol 13, No 2 (2023) |
ORIGINAL REPORTS |
Phenotypic variability in TRPV4-associated neuropathies and neuronopathies: a case series |
(Rus)
|
