| Issue |
Section |
Title |
File |
| Vol 10, No 4 (2016) |
Original articles |
Transplantation of neuronal precursors derived from induced pluripotent stem cells into the striatum of rats with the toxin-induced model of Huntington’s disease |
(Rus)
|
| Vol 10, No 2 (2016) |
Technologies |
Microelectrode recording of neuronal activity in the surgery for Parkinson’s disease |
(Rus)
|
| Vol 10, No 2 (2016) |
Original articles |
Evaluation of the effects of new peptide compounds in experimental animals with a toxic model of Alzheimer’s disease |
(Rus)
|
| Vol 10, No 1 (2016) |
Reviews |
A role of genetic factors in the development of individual predisposition to ischemic stroke |
(Rus)
|
| Vol 9, No 4 (2015) |
Reviews |
A genome editing technology and capabilities of its application in cellular neurobiology |
(Rus)
|
| Vol 9, No 4 (2015) |
Original articles |
The range of neurological syndromes associated with glutamic acid decarboxylase antibodies |
(Rus)
|
| Vol 9, No 3 (2015) |
Original articles |
Experience of experimental simulation of Huntington’s disease |
(Rus)
|
| Vol 9, No 2 (2015) |
Original articles |
Morphochemical evaluation of neurotransplantation outcomes in experimental Parkinsonism |
(Rus)
|
| Vol 9, No 2 (2015) |
Original articles |
Reorganization of the brain’s default mode network in patients with Parkinson’s disease: resting-state fMRI-based analysis of individual components |
(Rus)
|
| Vol 8, No 4 (2014) |
Original articles |
Clinical-sonographic and neurophysiological comparisons in hereditary motor and sensory neuropathy |
(Rus)
|
| Vol 7, No 4 (2013) |
Technologies |
Resting-state fMRI: new possibilities for studying physiology and pathology of the brain |
(Rus)
|
| Vol 7, No 4 (2013) |
Original articles |
Experience of using MRI morphometry in Huntington’s disease |
(Rus)
|
| Vol 7, No 2 (2013) |
Reviews |
Genetics of hereditary forms of dystonia |
(Rus)
|
| Vol 7, No 2 (2013) |
Technologies |
Current means for identifying the latent stage of a neurodegenerative process |
(Rus)
|
| Vol 6, No 4 (2012) |
Original articles |
A platform for studies of Huntington’s disease on the basis of induced pluripotent stem cells |
(Rus)
|
| Vol 6, No 4 (2012) |
Original articles |
MRI morphometry in primary focal dystonia |
(Rus)
|
| Vol 6, No 2 (2012) |
Original articles |
Neuropsychological abnormalities in early-stage Parkinson’s disease |
(Rus)
|
| Vol 5, No 4 (2011) |
Technologies |
Induced pluripotent stem cells: new possibilities in neurobiology and neurotransplantaion |
(Rus)
|
| Vol 5, No 4 (2011) |
Original articles |
Recurrent facial nerve neuropathies: clinical, electrophysiological and molecular analysis |
(Rus)
|
| Vol 4, No 4 (2010) |
Technologies |
Possibilities of transcranial sonography in extrapyramidal disorders |
(Rus)
|
| Vol 2, No 2 (2008) |
Clinical analysis |
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)
|
| Vol 2, No 2 (2008) |
Technologies |
Perspectives of nanotechnologies in clinical neurology |
(Rus)
|
| Vol 1, No 4 (2007) |
Technologies |
Voxel-guided morphometry: a new method for assessment of local secondary atrophic changes of the brain |
(Rus)
|
| Vol 1, No 4 (2007) |
Original articles |
Congenital pathological tortuosity of the internal carotid artery: population screening and genetic aspects |
(Rus)
|
| Vol 1, No 2 (2007) |
Clinical analysis |
Familial case of ataxia with oculomotor apraxia: first observation in Russian population |
(Rus)
|
| Vol 1, No 1 (2007) |
Original articles |
Heterogeneity of sporadic Parkinson’s disease: molecular approach to solving the problem |
(Rus)
|
| Vol 11, No 1 (2017) |
Clinical analysis |
Atypical clinical cases of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) |
(Rus)
|
| Vol 11, No 2 (2017) |
Original articles |
Assessment of the effects of cellular therapy on reproduction of the conditioned passive avoidance reflex in rats with quinoline-induced model of Huntington’s disease |
(Rus)
|
| Vol 12, No 4 (2018) |
Original articles |
Identification of Niemann–Pick type C disease in the group of ataxias of unclear origin in adults |
(Rus)
|
| Vol 12, No 5S (2018) |
Reviews |
Neurotransplantation: the time has come? |
(Rus)
|
| Vol 12, No 5S (2018) |
Reviews |
Influence of genetic factors on neurophysiological mechanisms of neurodegenerative diseases |
(Rus)
|
| Vol 12, No 5S (2018) |
Reviews |
Modeling of age-dependent disorders: relationship between the nervous and endocrine systems |
(Rus)
|
| Vol 13, No 1 (2019) |
Original articles |
Myotonic dystrophy: genetics and clinical polymorphism |
(Rus)
|
| Vol 13, No 2 (2019) |
Original articles |
Sensory ataxic neuropathy, dysarthria and ophthalmoparesis (SANDO syndrome): characteristics of a series of clinical observations in Russia |
(Rus)
|
| Vol 13, No 3 (2019) |
Original articles |
Cluster analysis of immunological serum markers in patients with Parkinson’s disease |
(Rus)
|
| Vol 13, No 4 (2019) |
Technologies |
New MRI diagnostic methods in Parkinson's disease: evaluating nigral degeneration |
(Rus)
|
| Vol 14, No 1 (2020) |
Original articles |
The use of a pharmabiotic based on the Lactobacillus fermentum U-21 strain to modulate the neurodegenerative process in an experimental model of Parkinson disease |
(Rus)
|
| Vol 14, No 2 (2020) |
Technologies |
Frontotemporal Dementia Rating Scale (FTD-FRS): Linguistic and Cultural Adaptation in Russia |
(Rus)
|
| Vol 14, No 4 (2020) |
Original articles |
Atypical (deafferentation) odontalgia |
(Rus)
|
| Vol 14, No 4 (2020) |
Reviews |
DNA methylation in Parkinson disease |
(Rus)
|
| Vol 15, No 1 (2021) |
Original articles |
Giftedness and cytoarchitecture of the prefrontal cortex of the outstanding scientist and physiologist I.P. Pavlov |
(Rus)
|
| Vol 15, No 2 (2021) |
Technologies |
Principles of personalized medicine and modern pharmaceutical technologies to optimize levodopa therapy of Parkinson's disease |
(Rus)
|
| Vol 16, No 2 (2022) |
Original articles |
First use of MRI-guided focused ultrasound to treat patients with essential tremor in Russia |
(Rus)
|
| Vol 16, No 1 (2022) |
Clinical analysis |
Corticobasal syndrome as a phenotype of various neurodegenerative disorders: a case series |
(Rus)
|
| Vol 17, No 1 (2023) |
Original articles |
Salivary gland immunohistochemistry vs substantia nigra sonography: comparative analysis of diagnostic significance |
(Rus)
|
| Vol 16, No 4 (2022) |
Original articles |
Identification of RNA markers associated with Parkinson's disease using multiplex gene expression analysis |
(Rus)
|
| Vol 17, No 2 (2023) |
Original articles |
Morphological Changes in Neural Progenitors Derived from Human Induced Pluripotent Stem Cells and Transplanted into the Striatum of a Parkinson's Disease Rat Model |
(Rus)
|
| Vol 17, No 4 (2023) |
Original articles |
MRI-Guided Focused Ultrasound in Cervical Dystonia |
(Rus)
(Eng)
|
| Vol 17, No 4 (2023) |
Original articles |
Assessment of Mitochondrial Gene Activity in Dopaminergic Neuron Cultures Derived from Induced Pluripotent Stem Cells Obtained from Parkinson's Disease Patients |
(Rus)
(Eng)
|
| Vol 18, No 2 (2024) |
Original articles |
Simultaneous dual-target magnetic resonance-guided focused ultrasound treatment for patients with tremor-dominant Parkinson’s disease |
(Rus)
(Eng)
|
СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).