41 results on '"Nikitin S"'
Search Results
2. Transcranial magnetic stimulation in assessing the functional capacity of the corticospinal tract in children
3. 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
4. Clinical and genetic characteristics of type 7 distal arthrogryposis caused by a pathogenic variant in the MYH8 gene
5. Socioeconomic efficiency of neonatal screening for spinal muscular atrophy in the Russian Federation
6. Reasons for misdiagnosis of polymyositis in patients with dysferlinopathy: a clinical case
7. Juvenile amyotrophic lateral sclerosis type 4: case report and review
8. The concept of “ambulatory” and “non-ambulatory” in patients with Duchenne muscular dystrophy: definitions and criteria
9. Diagnostic criteria for spinal muscular atrophy 5q
10. Phenotypic heterogeneity and diagnostic features of transthyretin amyloidosis with polyneuropathy
11. Russian-language dictionary of terms used in clinical electromyography and ultrasound examination of the neuromuscular system
12. EFFECTS OF 5-HYDROXYPYRIMIDINE DERIVATIVE ON GROWTH AND METASTASIS OF MELANOMA B16 IN C57BL/6 MICE
13. Clinical and genetic characteristics of distal arthrogryposis caused by mutations in the PIEZO2 gene
14. Clinical and genetic characteristics of type 3 lissencephaly caused by a mutation in the TUBA1A gene (OMIM: 611603)
15. Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia
16. The role of the ultrasound examination of the brachial plexus in thoracic outlet syndrome
17. Spinal and bulbar muscular atrophy with pseudomyotonia phenomena: a clinical case report
18. Clinical examination of patients with late-onset Pompe disease: typical and not typical symptoms and signs
19. Intraneural ganglion of the peroneal nerve: a report of 3 cases and literature review
20. Clinical and genetic characteristics of Nonaka myopathy (GNE-myopathy) in russian patients
21. Hysterical and comorbid mental disorders in outpatient neurological practice
22. Immunoglobulins in neurological practice: a review of the literature
23. The phenomenon of focal peripheral nerve constriction: review of the literature
24. Conduction block as an electrophysiological phenomenon: a review of the literature
25. Spinal muscular atrophy with lower limbs phenotype: clinical and genetic description of novel mutation in the DYNC1H1 gene
26. Prospective clinical and sonographic observation of the patient with hourglass-like focal radial nerve constriction
27. Misdiagnosed case of transthyretin amyloidosis in a fully investigated patient
28. Clinical and genetic characteristics of autosomal recessive axonal neuropathy with neuromyotonia in Russian patients
29. Bickerstaff brainstem encephalitis, acute transverse myelitis, and acute motor axonal neuropathy: diagnostic and treatment challenges in patients with concomitant syndromes. Clinical observation
30. Thoracic outlet syndrome: clinical and diagnostic features
31. Spectrum of sonographic changes in hereditary motor and sensory neuropathy with autosomal dominant and X-linked inheritance
32. New allelic variant of autosomal recessive hereditary motor and sensory neuropathy type 2S resulted from mutations in gene IGHMBP2
33. Laboratory studies and Pompe disease: from suspicion to therapy monitoring
34. Clinical Practice Guidelines for delivery of healthcare to patients with Pompe disease
35. A case of Becker myotonia with pseudodominant inheritance: сurrent approaches to the differential diagnosis of Thomsen’s and Becker's myotonia congenita
36. Nerve sonography in multifocal motor neuropathy and chronic inflammatory demyelinating polyneuropathy
37. THE SONOGRAPHIC DYNAMICS OF PERIPHERAL NERVES CROSS SECTIONAL AREA CHANGES IN MULTIFOCAL MOTOR NEUROPATHY TREATED WITH INTRAVENOUS IMMUNOGLOBULIN: CASE REPORT
38. Late-onset Pompe disease with phenotype of the limb-girdle muscular dystrophy
39. RESEARCH OF NEUROMUSCULAR PATHOLOGY IN RUSSIA. BACKGROUND AND PERSPECTIVES
40. ELECTROMYOGRAPHIC STAGES OF DENERVATION/REINNERVATION PROCESS IN NEUROMUSCULAR DISEASES: NEED FOR REVISION
41. A familial case of segregation of motor sensory neuropathy type 1B with multiple exostoses in monozygous twins
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