| Issue |
Section |
Title |
File |
| Vol 4, No 1 (2014) |
CLINICAL DISCUSSION |
Late-onset Pompe disease: first clinical description in Russia |
(Rus)
|
| Vol 4, No 3 (2014) |
LECTURES AND REVIEWS |
Adequate managment of patients with dystrophinopathies (muscular dystrophy Duchenne/Becker): objective scales and additional diagnostic methods |
(Rus)
|
| Vol 3, No 3 (2013) |
ORIGINAL REPORTS |
Botulinum toxin type A chemodenervation treatment in spastic forms of cerebral palsy |
(Rus)
|
| Vol 3, No 4 (2013) |
LECTURES AND REVIEWS |
Botulinum neurotoxin and chronic migraine: muscle fiber chemodenervation or nociceptic system modulation? |
(Rus)
|
| Vol 3, No 4 (2013) |
ORIGINAL REPORTS |
Electromyography in diagnostic of median nerve lesion in carpal tunnel syndrome of children with mucopolysaccharidoses |
(Rus)
|
| Vol 2, No 2 (2012) |
ORIGINAL STUDIES |
Specific features of chronic inflammatory demyelinating polyneuropathy in children |
(Rus)
|
| Vol 2, No 2 (2012) |
ORIGINAL STUDIES |
Intraoperative assesment of spinal cord conduction during surgical decompression in patients with cervical spondylotic myelopathy |
(Rus)
|
| Vol 2, No 3 (2012) |
ORIGINAL REPORTS |
Experience of polymyositis and antisynthetase syndrome treatment with rituximab |
(Rus)
|
| Vol 5, No 1 (2015) |
CLINICAL DISCUSSION |
A familial case of segregation of motor sensory neuropathy type 1B with multiple exostoses in monozygous twins |
(Rus)
|
| Vol 5, No 2 (2015) |
LECTURES AND REVIEWS |
Electromyographic stages of denervation/reinnervation process in neuromuscular diseases: need for revision |
(Rus)
|
| Vol 5, No 2 (2015) |
ИЗ ИСТОРИИ НЕВРОЛОГИИ |
Research of neuromuscular pathology in Russia. Background and perspectives |
(Rus)
|
| Vol 5, No 3 (2015) |
CLINICAL DISCUSSION |
Late-onset Pompe disease with phenotype of the limb-girdle muscular dystrophy |
(Rus)
|
| Vol 6, No 1 (2016) |
LECTURES AND REVIEWS |
Clinical Practice Guidelines for delivery of healthcare to patients with Pompe disease |
(Rus)
|
| Vol 6, No 1 (2016) |
LECTURES AND REVIEWS |
Laboratory studies and Pompe disease: from suspicion to therapy monitoring |
(Rus)
|
| Vol 6, No 1 (2016) |
ORIGINAL REPORTS |
Nerve sonography in multifocal motor neuropathy and chronic inflammatory demyelinating polyneuropathy |
(Rus)
|
| Vol 6, No 1 (2016) |
CLINICAL DISCUSSION |
A case of Becker myotonia with pseudodominant inheritance: сurrent approaches to the differential diagnosis of Thomsen’s and Becker's myotonia congenita |
(Rus)
|
| Vol 6, No 1 (2016) |
OBITUARY |
In memory of professor Irena Gausmanova-Petrusevich (1917–2015) |
(Rus)
|
| Vol 6, No 2 (2016) |
ORIGINAL REPORTS |
Spectrum of sonographic changes in hereditary motor and sensory neuropathy with autosomal dominant and X-linked inheritance |
(Rus)
|
| Vol 6, No 2 (2016) |
CLINICAL DISCUSSION |
New allelic variant of autosomal recessive hereditary motor and sensory neuropathy type 2S resulted from mutations in gene IGHMBP2 |
(Rus)
|
| Vol 6, No 4 (2016) |
CLINICAL DISCUSSION |
THE SONOGRAPHIC DYNAMICS OF PERIPHERAL NERVES CROSS SECTIONAL AREA CHANGES IN MULTIFOCAL MOTOR NEUROPATHY TREATED WITH INTRAVENOUS IMMUNOGLOBULIN: CASE REPORT |
(Rus)
|
| 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 1 (2018) |
CLINICAL DISCUSSION |
Misdiagnosed case of transthyretin amyloidosis in a fully investigated patient |
(Rus)
|
| Vol 8, No 2 (2018) |
ORIGINAL REPORTS |
Spinal muscular atrophy with lower limbs phenotype: clinical and genetic description of novel mutation in the DYNC1H1 gene |
(Rus)
|
| Vol 8, No 2 (2018) |
ORIGINAL REPORTS |
Prospective clinical and sonographic observation of the patient with hourglass-like focal radial nerve constriction |
(Rus)
|
| Vol 9, No 1 (2019) |
LECTURES AND REVIEWS |
Conduction block as an electrophysiological phenomenon: a review of the literature |
(Rus)
|
| Vol 9, No 1 (2019) |
LECTURES AND REVIEWS |
The phenomenon of focal peripheral nerve constriction: review of the literature |
(Rus)
|
| Vol 9, No 1 (2019) |
LECTURES AND REVIEWS |
Immunoglobulins in neurological practice: a review of the literature |
(Rus)
|
| Vol 9, No 2 (2019) |
ORIGINAL REPORTS |
Hysterical and comorbid mental disorders in outpatient neurological practice |
(Rus)
|
| Vol 9, No 3 (2019) |
CLINICAL DISCUSSION |
Clinical and genetic characteristics of Nonaka myopathy (GNE-myopathy) in russian patients |
(Rus)
|
| Vol 9, No 4 (2019) |
LECTURES AND REVIEWS |
Clinical examination of patients with late-onset Pompe disease: typical and not typical symptoms and signs |
(Rus)
|
| Vol 9, No 4 (2019) |
CLINICAL DISCUSSION |
Spinal and bulbar muscular atrophy with pseudomyotonia phenomena: a clinical case report |
(Rus)
|
| Vol 10, No 1 (2020) |
ORIGINAL REPORTS |
The role of the ultrasound examination of the brachial plexus in thoracic outlet syndrome |
(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 |
Clinical and genetic characteristics of type 3 lissencephaly caused by a mutation in the TUBA1A gene (OMIM: 611603) |
(Rus)
|
| Vol 11, No 2 (2021) |
CLINICAL DISCUSSION |
Clinical and genetic characteristics of distal arthrogryposis caused by mutations in the PIEZO2 gene |
(Rus)
|
| Vol 11, No 3 (2021) |
LECTURES AND REVIEWS |
Phenotypic heterogeneity and diagnostic features of transthyretin amyloidosis with polyneuropathy |
(Rus)
|
| Vol 11, No 3 (2021) |
ORIGINAL REPORTS |
Diagnostic criteria for spinal muscular atrophy 5q |
(Rus)
|
| Vol 11, No 3 (2021) |
ORIGINAL REPORTS |
Russian-language dictionary of terms used in clinical electromyography and ultrasound examination of the neuromuscular system |
(Rus)
|
| Vol 12, No 2 (2022) |
LECTURES AND REVIEWS |
The concept of “ambulatory” and “non-ambulatory” in patients with Duchenne muscular dystrophy: definitions and criteria |
(Rus)
|
| Vol 12, No 2 (2022) |
ORIGINAL REPORTS |
Differential diagnosis of myopathy and multiple epiphysal dysplasia caused by mutations in the COMP gene in children |
(Rus)
(Eng)
|
| Vol 12, No 3 (2022) |
CLINICAL DISCUSSION |
Juvenile amyotrophic lateral sclerosis type 4: case report and review |
(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) |
LECTURES AND REVIEWS |
Consensus concept of modern effective therapy for Duchenne muscular dystrophy |
(Rus)
|
| Vol 13, No 2 (2023) |
ORIGINAL REPORTS |
Phenotypic variability in TRPV4-associated neuropathies and neuronopathies: a case series |
(Rus)
|
| Vol 13, No 2 (2023) |
ORIGINAL REPORTS |
Clinical and genetic characteristics of primary hypertrophic osteoarthropathy |
(Rus)
|
| Vol 13, No 3 (2023) |
ORIGINAL REPORTS |
Socioeconomic efficiency of neonatal screening for spinal muscular atrophy in the Russian Federation |
(Rus)
|
| Vol 13, No 3 (2023) |
CLINICAL DISCUSSION |
Clinical and genetic characteristics of the first Russian patient with a syndrome of craniofacial dysmorphia-deafness-anomalies of the upper limbs, caused by a mutation in the PAX3 gene |
(Rus)
|
| Vol 13, No 3 (2023) |
CLINICAL DISCUSSION |
Clinical and genetic characteristics of type 7 distal arthrogryposis caused by a pathogenic variant in the MYH8 gene |
(Rus)
|
| Vol 14, No 2 (2024) |
ORIGINAL REPORTS |
Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene |
(Rus)
(Eng)
|
| Vol 14, No 2 (2024) |
LECTURES AND REVIEWS |
Transcranial magnetic stimulation in assessing the functional capacity of the corticospinal tract in children |
(Rus)
|
| Vol 14, No 4 (2024) |
LECTURES AND REVIEWS |
Research and clinical application of transcranial magnetic stimulation in children with head injury: method overview |
(Rus)
|
| Vol 15, No 1 (2025) |
ORIGINAL REPORTS |
Assessment of walking in patients with Duchenne muscular dystrophy receiving ataluren in real clinical practice |
(Rus)
|
| Vol 15, No 2 (2025) |
CLINICAL DISCUSSION |
Suppression of segmental cervical motor evoked potential in postanoxic encephalopathy in a child: clinical case |
(Rus)
|
