I. Ivanova-Smolenskaya

发表

Trinucleotide repeat length and rate of progression of Huntington's disease

Osamu Onodera, Shuichi Igarashi, S. Tsuji, 1994, Annals of neurology.

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.

T. Gilliam, G. Penchaszadeh, O. Evgrafov, 1997, American journal of human genetics.

A Simple and Rapid Method for Detection of the 1069Gln Mutation in Wilson Disease

S. Limborska, P. Slominsky, I. Ivanova-Smolenskaya, 2002, Russian Journal of Genetics.

The His1069Gln mutation in the ATP7B gene in Russian patients with Wilson disease

I. Ovchinnikov, S. Illarioshkin, E. Markova, 1999, Journal of medical genetics.

A common 3‐bp deletion in the DYT1 gene in Russian families with early‐onset torsion dystonia

S. Limborska, S. Illarioshkin, P. Slominsky, 1999, Human mutation.

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

A. Brice, S. Limborska, M. Periquet, 2003, Movement disorders : official journal of the Movement Disorder Society.

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

A. Brice, S. Illarioshkin, E. Markova, 2000, Journal of Neurology.

Spinocerebellar ataxia type 1 in Russia

I. Ovchinnikov, S. Illarioshkin, E. Markova, 1996, Journal of Neurology.

Analysis of known point mutations and SNPs in genes responsible for monogenic Parkinson’s disease in Russian patients

S. Limborska, P. Slominsky, S. Illarioshkin, 2013 .

A novel mutation in the GTP cyclohydrolase I gene associated with a broad range of clinical presentations in a family with autosomal dominant dopa‐responsive dystonia

S. Limborska, P. Slominsky, S. Popova, 1999, European journal of neurology.

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

S. Tsuji, S. Limborska, P. Slominsky, 1998, Archives of neurology.

Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy

V. Sukhorukov, C. Greenberg, S. Illarioshkin, 2000, Neurology.

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

C. Walsh, S. Tsuji, J. Gleeson, 1999, Journal of Neurology.

Peculiarities of Carnosine Metabolism in a Patient with Pronounced Homocarnosinemia

E. Markova, I. Ivanova-Smolenskaya, G. Kramarenko, 2001, Bulletin of Experimental Biology and Medicine.

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

S. Limborska, S. Illarioshkin, E. Markova, 2007, European journal of neurology.

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

S. Tsuji, K. Bulayeva, S. Limborska, 1996, Brain : a journal of neurology.

Different phenotypes of Friedreich's ataxia within one ‘pseudo‐dominant’ genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features

I. Ovchinnikov, S. Illarioshkin, E. Markova, 2000, European journal of neurology.

Carnosine [corrected] increases efficiency of DOPA therapy of Parkinson's disease: a pilot study.

I. Ivanova-Smolenskaya, A. Boldyrev, G. Bagyeva, 2008, Rejuvenation research.

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.

N. Risch, M. Brin, X. Breakefield, 1998, Human molecular genetics.

Molecular Genetic Analysis of Hereditary Neurodegenerative Diseases

S. Limborska, P. Slominsky, S. Illarioshkin, 2004, Russian Journal of Genetics.

Molecular Genetic Analysis of Essential Tremor

A. Brice, S. Limborska, S. Illarioshkin, 2002, Russian Journal of Genetics.

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

S. Tsuji, Hajime Tanaka, H. Tanaka, 1997, Genomics.

Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium.

N. Risch, M. Brin, J. Gusella, 1997, Genome research.

Carnisone Increases Efficiency of DOPA Therapy of Parkinson ’ s Disease : A Pilot Study

I. Ivanova-Smolenskaya, A. Boldyrev, G. Bagyeva, 2008 .

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

S. Limborska, S. Illarioshkin, I. Ivanova-Smolenskaya, 2010, Neuroscience Letters.

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

S. Illarioshkin, Y. Varakin, B. Baziyan, 2015, Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova.

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

S. Limborska, S. Illarioshkin, I. Ivanova-Smolenskaya, 2012, Movement disorders : official journal of the Movement Disorder Society.

Expression of GSK3B in peripheral blood of patients with Parkinson’s disease

S. Limborska, S. Illarioshkin, P. Slominsky, 2011, Molecular Biology.

Characteristics of Learning Voluntary Control of Posture in Lesions of the Pyramidal and Nigrostriatal Systems

M. Ioffe, L. Chernikova, Ksenia I. Ustinova, 2004, Neuroscience and Behavioral Physiology.

Therapeutic Efficacy of the Neuroprotective Plant Adaptogen in Neurodegenerative Disease (Parkinson’s Disease as an Example)

E. Bocharov, I. Ivanova-Smolenskaya, V. Kucheryanu, 2010, Bulletin of Experimental Biology and Medicine.

Spectral electromyographic analysis of essential tremor.

Andreeva Ea, I. Ivanova-Smolenskaya, Kandel' Ei, 1987, Neuroscience and behavioral physiology.

Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan

A. Brice, G. Stevanin, S. Illarioshkin, 2000, Movement disorders : official journal of the Movement Disorder Society.