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List of works by Sergey Illarioshkin

A 30-year history of MPAN case from Russia.

scientific article published on 2 June 2017

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia

scientific article published on 01 April 2007

Alpha-theta border EEG abnormalities in preclinical Huntington's disease

scientific article published on 24 June 2014

Analysis of PARK2 gene exon rearrangements in Russian patients with sporadic Parkinson's disease

scientific article published on 13 September 2011

Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology

scientific article published on 28 July 2006

Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations

scientific article published on 01 August 2018

C9ORF72 hexanucleotide repeat expansion in ALS patients from the Central European Russia population

scientific article published on 09 July 2015

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

scientific article published in December 1996

Current advances in cell electrophysiology: applications for the analysis of intercellular communications within the neurovascular unit

scientific article published on 7 December 2015

Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage.

scientific article

Experience of experimental modelling of Huntington’s disease

Expression analysis of suppression of tumorigenicity 13 gene in patients with Parkinson's disease.

scientific article published in March 2010

Functional properties of dopaminergic neurons obtained from fibroblasts of a patient with PARK2 form of Parkinson's disease

scientific article published in January 2015

Genetic studies of Russian patients with amyotrophic lateral sclerosis

scientific article published on 9 November 2015

Investigation of the effects of GABA receptor agonists in the differentiation of human induced pluripotent stem cells into dopaminergic neurons.

scientific article published in September 2016

Involvement of endocytosis and alternative splicing in the formation of the pathological process in the early stages of Parkinson's disease.

scientific article

Lack of alpha-synuclein gene mutations in families with autosomal dominant Parkinson's disease in Russia

scientific article published on 01 December 2000

Levodopa-carbidopa intestinal gel in the treatment of patients with Parkinson disease: results of a 12-month open study

scientific article published in January 2017

Manifestation of Huntington's disease pathology in human induced pluripotent stem cell-derived neurons.

scientific article published on 14 April 2016

Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

scientific article published on 01 August 2003

New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

scientific article published on 17 January 2015

Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson's disease

scientific article published on 22 October 2016

Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects

scientific article published on 14 February 2001

Parkinson's Disease: Available Clinical and Promising Omics Tests for Diagnostics, Disease Risk Assessment, and Pharmacotherapy Personalization

scientific article published on 25 May 2020

Pharmacokinetics and pharmacodynamics of gastroretentive delivery of levodopa/carbidopa in patients with Parkinson disease

scientific article published on 01 March 2012

Pharmacokinetics of levodopa/carbidopa delivered from gastric-retentive extended-release formulations in patients with Parkinson's disease.

scientific article

Phenotypical Differences in Neuronal Cultures Derived via Reprogramming the Fibroblasts from Patients Carrying Mutations in Parkinsonian Genes LRRK2 and PARK2.

scientific article published on 31 October 2015

Potential Biomarkers of the Earliest Clinical Stages of Parkinson's Disease.

scientific article published on 21 September 2015

Quantitative EEG during normal aging: association with the Alzheimer's disease genetic risk variant in PICALM gene

scientific article published on 20 December 2016

Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.

scientific article published in June 1997

Research Center of Neurology — the 70-anniversary

scientific article published on 01 January 2015

Role of zinc and copper ions in the pathogenetic mechanisms of Alzheimer's and Parkinson's diseases

scientific article

Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene.

scientific article published on 31 October 2016

Spinocerebellar ataxia type 1 in Russia

scientific article published on 01 July 1996

Studies of the candidate genes in X-linked congenital cerebellar hypoplasia

scientific article published on 01 December 1999

TOR1A polymorphisms in a Russian cohort with primary focal/segmental dystonia

scientific article published on 2 October 2014

The GTP cyclohydrolase I gene in Russian families with dopa-responsive dystonia

scientific article published on 01 June 1998

The morphofunctional properties of induced pluripotent stem cells derived from human skin fibroblasts and differentiated to dopaminergic neurons

Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry.

scientific article published on 05 August 2015

X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome Xq.

scientific article published in July 1996

[C9orf72-associated frontotemporal dementia in the Russian population]

scientific article published on 01 January 2020

[Identification of people at the latent stage of Parkinson's disease (the PARKINLAR study): first results and an optimization of the algorithm].

scientific article

miRNA expression is highly sensitive to a drug therapy in Parkinson's disease.

scholarly article by Anelya Alieva et al published 2015 in Parkinsonism and Related Disorders

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