Capacities of the dopamine receptor agonist pramipexole in the treatment of patients with Parkinson’s disease by S N Illarioshkin

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Adult spinal muscular atrophy: problems of early diagnosis by Yu. A. Shpilyukova, S. N. Illarioshkin

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Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): literature review by E. P. Nuzhnyi, S. N. Illarioshkin

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Vladimir Karlov and the Research Center of Neurology: 70 years together by M. A. Piradov, S. A. Klyushnikov, S. N. Illarioshkin

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Spinal and bulbar muscular atrophy as a multisystem disease with motor neuron and muscle involvement: literature review and a case report by E. O. Ivanova, E. Yu. Fedotov, S. N. Illarioshkin

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Malingering and functional movement disorder by K. M. Evdokimov, E. Yu. Fedotova, S. N. Illarioshkin

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Sensitivity and Specificity of the Diagnostic Method for Detecting α-Synuclein as a Histological Marker for Parkinson's Disease in Salivary Gland Tissues: a Systematic Review and M... by Kristina K. Khacheva, Sergey N. Illarioshkin, Alexey V. Karabanov

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A case of Becker myotonia with pseudodominant inheritance: сurrent approaches to the differential diagnosis of Thomsen’s and Becker's myotonia congenita by S. A. Kurbatov, S. S. Nikitin, S. N. Illarioshkin, P. Gundorova, A. V. Polyakov

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The first family case of spinocerebellar ataxia type 14 in Russia by E. P. Nuzhnyy, N. Yu. Abramycheva, S. A. Klyushnikov, S. N. Illarioshkin

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Assessment of Mitochondrial Gene Activity in Dopaminergic Neuron Cultures Derived from Induced Pluripotent Stem Cells Obtained from Parkinson's Disease Patients by Anna S. Vetchinova, Marina R. Kapkaeva, Natalia M. Mudzhiri, Sergey N. Illarioshkin

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Gerstmann–Sträussler–Scheinker syndrome with early-onset spinocerebellar ataxia phenotype by E. P. Nuzhnyi, N. Y. Abramycheva, E. Y. Fedotova, S. N. Illarioshkin

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Psychotic disorders in Parkinson's disease: phenomenology, pathogenesis, therapeutic approaches (modern view on the problem) by Kh. I. Alizade, A. A. Ragimova, E. Yu. Fedotova, S. N. Illarioshkin

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Mental disorders in Huntington’s disease by S. A. Klyushnikov, E. N. Yudina, S. N. Illarioshkin, I. A. Ivanova-Smolenskaya

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A case of chorea with cognitive impairment associated with polycythemia vera by Yu. A. Shpilyukova, O. V. Smetanina, A. A. Kolpina, S. N. Illarioshkin

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A variant of idiopathic epilepsy: Clinical note by V. A. Karlov, S. N. Illarioshkin, G. A. Kovalenko, N. Yu. Abramycheva

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Presymptomatic genetic counseling in amyotrophic lateral sclerosis by Yu. A. Shpilyukova, A. A. Rosliakova, M. N. Zakharova, S. N. Illarioshkin

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Neurological manifestations of hypoparathyroidism: diagnostic difficulties. Case report by Evgenii P. Nuzhnyi, Ksenia V. Antonova, Marine M. Tanashyan, Sergey N. Illarioshkin

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Rapidly progressive dementia with early onset associated with the I143T mutation in the PSEN1 gene: a clinical case in a family from Russia by Yu. A. Shpilyukova, A. O. Protopopova, N. Yu. Abramycheva, E. Yu. Fedotova, S. N. Illarioshkin

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Accelerometry in Diagnosis of Functional Tremor by Konstantin M. Evdokimov, Ekaterina O. Ivanova, Amayak G. Brutyan, Ekaterina Y. Fedotova, Sergey N. Illarioshkin

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Anomia: Deciphering Functional Neuroanatomy in Primary Progressive Aphasia Variants by Diliara R. Akhmadullina, Rodion N. Konovalov, Yulia A. Shpilyukova, Ekaterina Yu. Fedotova, Sergey N. Illarioshkin

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