Evgenii P. Nuzhnyi
Moscow, MOW, Russian Federation
Last Updated: 09/26/2026
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Found 19 publications
Rare forms of autosomal recessive spinocerebellar ataxia associated with mutations in the ANO10 (ATX-ANO10) and SYNE1 (ATX-SYNE1) genes
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: September 13, 2024
Cytokine profile and case series of tract-specific myelitis following SARS-CoV-2 infection.
Journal: Current journal of neurology
Published: June 06, 2024
Case report: A novel CACNA1S mutation associated with hypokalemic periodic paralysis.
Journal: Frontiers in neurology
Published: July 26, 2023
Cerebellar degeneration associated with HIV infection
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: June 14, 2023
Spinocerebellar ataxia type 8 in Russian patients
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: August 29, 2022
Neurological manifestations of hypoparathyroidism: diagnostic difficulties. Case report
Journal: Terapevticheskii arkhiv
Published: May 14, 2022
Mutation analysis of the TATA box-binding protein (TBP) gene in Russian patients with spinocerebellar ataxia and Huntington disease-like phenotype.
Journal: Clinical neurology and neurosurgery
Published: May 09, 2022
A rare case of neurosyphilis presenting as generalized dystonia with bilateral cerebellar infarctions.
Journal: Current journal of neurology
Published: March 03, 2022
Neurogenic overactive bladder: focus on cognitive function
Journal: Urologiia (Moscow, Russia : 1999)
Published: November 07, 2021
Immune-mediated ataxia with cerebellar hemiatrophy and dystonia associated with Castleman disease.
Journal: Clinical neurology and neurosurgery
Published: September 08, 2020
POLG-associated ataxias can represent a substantial part of recessive and sporadic ataxias in adults.
Journal: Clinical neurology and neurosurgery
Published: June 13, 2020
Last Updated: 09/26/2026