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Hereditary spastic paraplegias

Nervno-myshechnye bolezni, 2024-01, Vol.13 (4), p.74-82

2024

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Depression and Anxiety in Parkinson’s Disease

Neuroscience and behavioral physiology, 2018-06, Vol.48 (5), p.636-640

2018

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Clinical and epidemiological characteristics of hereditary motor-sensory neuropathy 1X caused by the mutation c. 259C> G (p. P87A) in the GJB1 gene of patients from the Republic of Bashkortostan

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2017, Vol.117 (3), p.80

2017

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Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia

Russian journal of genetics, 2016-06, Vol.52 (6), p.603-607

2016

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Analysis of COL1A1 and COL1A2 genes in osteogenesis imperfecta patients from Russia

Bone (New York, N.Y.), 2012-05, Vol.50, p.S109-S109

2012

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Association of cytokine gene polymorphisms in peptic ulcer development in the Bashkortostan Republic

Russian journal of genetics, 2014-12, Vol.50 (12), p.1316-1325

2014

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Role of allelic genes of matrix metalloproteinases and their tissue inhibitors in the risk of peptic ulcer disease development

Russian journal of genetics, 2016-03, Vol.52 (3), p.320-330

2016

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Role of Allelic Genes of Matrix Metalloproteinases and Their Tissue Inhibitors in the Peptic Ulcer Disease Development

Genetika, 2016-03, Vol.52 (3), p.364

2016

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The role of genetic factors in levodopa-induced dyskinesias development in Russian patients with Parkinson's disease: A pilot study

Journal of the neurological sciences, 2019-10, Vol.405, p.42-42

2019

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MFN2 Gene Analysis in Patients with Hereditary Motor and Sensory Neuropathy from Bashkortostan Republic

Генетика, 2013-07, Vol.49 (7), p.884-890

2013

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Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia

Actanaturae, 2011-07, Vol.3 (3), p.52-63

2011

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MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic

Russian journal of genetics, 2013-07, Vol.49 (7), p.771-777

2013

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A biobank for Parkinson's disease and atypical parkinsonism in central Asian and Transcaucasian regions

Lancet neurology, 2024-09, Vol.23 (9), p.859-860

2024

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Amyotrophic lateral sclerosis associated with a new pathogenic variant of the ERBB4 gene

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2024, Vol.124 (7), p.165

2024

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Study of the Role of Genes Involved in the Metabolism of Histamine in the Development of Allergic Respiratory Diseases

Russian journal of genetics, 2024-03, Vol.60 (3), p.352-359

2024

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Genetic epidemiological study of Bashkortostan Republic: The effect of genetic structure of population on the load of monogenic hereditary diseases

Russian journal of genetics, 2009-04, Vol.45 (4), p.478-485

2009

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M06Epidemiology of Huntington's disease in the Republic of Bashkortostan

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A48-et-A48

2012

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M06 Epidemiology of Huntington's disease in the Republic of Bashkortostan

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A48-A48

2012

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Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia

Russian journal of genetics, 2022-09, Vol.58 (9), p.1145-1153

2022

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Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan

Russian journal of genetics, 2008-10, Vol.44 (10), p.1201-1207

2008

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The Genome Structure and DNA Diagnosis of Monogenic Hereditary Disorders in the Volga–Ural Region

Molecular biology (New York), 2004-01, Vol.38 (1), p.119-127

2004

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Association analysis of serotonin system gene polymorphisms (5-HTT, HTR1B, HTR2A, HTR2C, and TPH1) with the risk of Parkinson's disease in Tatars

Yakut Medical Journal, 2021 (4), p.14-19

2021

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Major Mutation in the SPAST Gene in Patients with Autosomal Dominant Spastic Paraplegia from the Republic of Bashkortostan

Russian journal of genetics, 2019-02, Vol.55 (2), p.259-262

2019

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Prevalence of mutation C.11864g >a in the Ush2a gene in patients with Usher Ii syndrome from Volga-ural region of Russia

Archives of disease in childhood, 2014-10, Vol.99 (10), p.A475

2014

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PO-0675Prevalence Of Mutation C.11864g >a (p. Trp3955x) In The Ush2a Gene In Patients With Usher Ii Syndrome From Volga-ural Region Of Russia

Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A475-A475

2014

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Hereditary spastic paraplegias

Depression and Anxiety in Parkinson’s Disease

Clinical and epidemiological characteristics of hereditary motor-sensory neuropathy 1X caused by the mutation c. 259C> G (p. P87A) in the GJB1 gene of patients from the Republic of Bashkortostan

Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia

Analysis of COL1A1 and COL1A2 genes in osteogenesis imperfecta patients from Russia

Association of cytokine gene polymorphisms in peptic ulcer development in the Bashkortostan Republic

Role of allelic genes of matrix metalloproteinases and their tissue inhibitors in the risk of peptic ulcer disease development

Role of Allelic Genes of Matrix Metalloproteinases and Their Tissue Inhibitors in the Peptic Ulcer Disease Development

The role of genetic factors in levodopa-induced dyskinesias development in Russian patients with Parkinson's disease: A pilot study

MFN2 Gene Analysis in Patients with Hereditary Motor and Sensory Neuropathy from Bashkortostan Republic

Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia

MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic

A biobank for Parkinson's disease and atypical parkinsonism in central Asian and Transcaucasian regions

Amyotrophic lateral sclerosis associated with a new pathogenic variant of the ERBB4 gene

Study of the Role of Genes Involved in the Metabolism of Histamine in the Development of Allergic Respiratory Diseases

Genetic epidemiological study of Bashkortostan Republic: The effect of genetic structure of population on the load of monogenic hereditary diseases

M06Epidemiology of Huntington's disease in the Republic of Bashkortostan

M06 Epidemiology of Huntington's disease in the Republic of Bashkortostan

Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia

Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan

The Genome Structure and DNA Diagnosis of Monogenic Hereditary Disorders in the Volga–Ural Region

Association analysis of serotonin system gene polymorphisms (5-HTT, HTR1B, HTR2A, HTR2C, and TPH1) with the risk of Parkinson's disease in Tatars

Major Mutation in the SPAST Gene in Patients with Autosomal Dominant Spastic Paraplegia from the Republic of Bashkortostan

Prevalence of mutation C.11864g >a in the Ush2a gene in patients with Usher Ii syndrome from Volga-ural region of Russia

PO-0675Prevalence Of Mutation C.11864g >a (p. Trp3955x) In The Ush2a Gene In Patients With Usher Ii Syndrome From Volga-ural Region Of Russia

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