Author Details

Иллариошкин, С.

Issue Section Title File
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 PDF
(Rus)
Vol 6, No 4 (2016) ORIGINAL REPORTS MOLECULAR STRUCTURE OF AMYOTROPHIC LATERAL SCLEROSIS IN RUSSIAN POPULATION PDF
(Rus)
Vol 7, No 4 (2017) CLINICAL DISCUSSION Presymptomatic genetic counseling in amyotrophic lateral sclerosis PDF
(Rus)
Vol 8, No 2 (2018) ORIGINAL REPORTS Evaluation of methylation status of the 5’-promoter region of C9orf72 gene in Russian patients with neurodegenerative diseases PDF
(Rus)
Vol 10, No 1 (2020) CLINICAL DISCUSSION Spinal and bulbar muscular atrophy as a multisystem disease with motor neuron and muscle involvement: literature review and a case report PDF
(Rus)
Vol 10, No 3 (2020) LECTURES AND REVIEWS Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): literature review PDF
(Rus)
Vol 10, No 3 (2020) ORIGINAL REPORTS Genetic model of motor neuron disease in B6SJL-Tg mice: new data on the dynamics of motor symptoms and immunohistochemical manifestations of the neurodegenerative process PDF
(Rus)
Vol 12, No 3 (2022) CLINICAL DISCUSSION The first family case of spinocerebellar ataxia type 14 in Russia PDF
(Rus)
Vol 12, No 4 (2022) ORIGINAL REPORTS Adult spinal muscular atrophy: problems of early diagnosis PDF
(Rus)
Vol 13, No 4 (2023) ORIGINAL REPORTS Безопасность и эффективность авалглюкозидазы альфа по сравнению с алглюкозидазой альфа у пациентов с болезнью Помпе с поздним началом: рандомизированное многоцентровое исследование III фазы COMET PDF
(Rus)