Published in Patol Fiziol Eksp Ter on February 24, 2012
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Neural coding of finger and wrist movements. J Comput Neurosci (1999) 1.01
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Responses of human masseter motor units to stretch. J Physiol (1995) 0.85
Symmetric force response of human masticatory muscles to stretch and unloading. Exp Brain Res (1997) 0.85
[Diagnostics of keratitis-ichthyosis-deafness syndrome (KID- syndrome)]. Vestn Otorinolaringol (2012) 0.84
An apparatus for controlled stretch of human jaw-closing muscles. J Neurosci Methods (1993) 0.81
[DNA diagnosis in congenital and early childhood hypoacusis and deafness]. Vestn Otorinolaringol (2002) 0.79
Functional identification of the input-output transforms of mammalian motoneurones. J Physiol Paris (1999) 0.79
[The results of audiological examination of children presenting with sensorineural loss of hearing due to GJB2 gene mutations during the first year of life]. Vestn Otorinolaringol (2011) 0.79
[The spectrum of CLCN1 gene mutations in patients with nondystrophic Thomsen's and Becker's myotonias]. Genetika (2012) 0.78
Different morbilliviruses in European and Siberian seals. Vet Rec (1990) 0.78
[The cascade scheme as a methodical platform for analysis of health risks in space flight and partially and fully analog conditions]. Aviakosm Ekolog Med (2011) 0.77
[Prevalences of hereditary diseases in various populations in Russia]. Genetika (2007) 0.77
Cryoglobulin level in patients with ischemic stroke and effect of selective plasmapheresis on this parameter. Bull Exp Biol Med (2005) 0.77
[The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns]. Genetika (2014) 0.76
[Genetic and clinical characteristics of 22q11.2 deletion syndrome]. Genetika (2014) 0.76
[Prevalence and molecular-genetic typing of nonsyndromal neurosensory deafness in the Chuvash Republic]. Genetika (2003) 0.76
Tract-based spatial statistical analysis of diffusion tensor imaging in pediatric patients with mitochondrial disease: widespread reduction in fractional anisotropy of white matter tracts. AJNR Am J Neuroradiol (2012) 0.76
[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness]. Genetika (2012) 0.76
[Infusion of drugs through the umbilical vein]. Vestn Khir Im I I Grek (1975) 0.75
[Hereditary motor and sensory neuropathy type 4A]. Zh Nevrol Psikhiatr Im S S Korsakova (2010) 0.75
[Experimental substantiation of the efficiency of using the stem and progenitory cells of the bone marrow for regulating the recovery processes in organs in acute and chronic affections]. Vestn Ross Akad Med Nauk (2004) 0.75
[An experimental infection of the seal Phoca sibirica with the morbilli virus]. Vopr Virusol (1992) 0.75
[The treatment of autoimmune thyroiditis using low-intensity laser radiation]. Vopr Kurortol Fizioter Lech Fiz Kult (1998) 0.75
[Morphological changes in retina and optic nerve head in patients with Leber's hereditary optic neuropathy]. Vestn Oftalmol (2014) 0.75
[New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance]. Genetika (2014) 0.75
[Clinical, genealogical and molecular genetic study of Emery-Dreifuss muscular dystrophy]. Zh Nevrol Psikhiatr Im S S Korsakova (2006) 0.75
[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]. Vestn Otorinolaringol (2014) 0.75
[Cryoglobulinemia and extracorporal plasma therapy in severe ischemic stroke]. Zh Nevrol Psikhiatr Im S S Korsakova (2004) 0.75
[Population frequency and age of c.806C > T mutation in CYB5R3 gene as cause of recessive congenital methemoglobinemia in Yakutia]. Genetika (2013) 0.75
[Heterozygous carrier rate for type I-IV proximal spinal muscular atrophy in Chuvashes, Udmurts, and residents of the Moscow region]. Genetika (2012) 0.75
[Autofibroblasts in surgical treatment of periodontal disease]. Stomatologiia (Mosk) (2013) 0.75
[Surgical treatment for autoimmune thyroiditis]. Khirurgiia (Mosk) (1999) 0.75
[THE PROSPECTS FOR USING SIMULATION TECHNOLOGIES ON MANNED SPACECRAFT FOR EFFECTIVE TRAINING AND REFRESHING COSMONAUTS' SKILLS IN PROVIDING THE EMERGENCY MEDICAL AID]. Aviakosm Ekolog Med (2015) 0.75
[Effect of bone marrow cells on colony-forming stromal cells in guinea pigs and on the proliferation of their cultured descendents]. Biull Eksp Biol Med (1988) 0.75
[Merosin-deficient congenital muscular dystrophy]. Zh Nevrol Psikhiatr Im S S Korsakova (2010) 0.75
[Prospects for the Use of Cells Possessing Myogenic Potential in the Treatment of Skeletal Muscle Diseases: a Review of Research. Part 2--Populations of stem cells of muscle and non-muscle origin]. Patol Fiziol Eksp Ter (2016) 0.75
[Hereditary optic neuropathies: clinical and molecular genetic characteristics]. Vestn Oftalmol (2014) 0.75
[Use of autogenous fibroblasts of human oral mucosa for gum recession treatment]. Stomatologiia (Mosk) (2013) 0.75
[Cryoglobulins in patients with ischemic stroke]. Zh Nevrol Psikhiatr Im S S Korsakova (2010) 0.75
[EMG-force relation during potentiation]. Biull Eksp Biol Med (1987) 0.75
[Sensorimotor neuropathy with X-linked dominant inheritance]. Zh Nevrol Psikhiatr Im S S Korsakova (2001) 0.75
[Antibodies to morbilli virus of the Baikal seal in its natural host]. Vopr Virusol (1991) 0.75
[The isolation of the morbilli virus from the Baikal seal Phoca sibirica and its preliminary characterization]. Vopr Virusol (1991) 0.75
[Fungal endocarditis after mitral-aortic prosthesis implantation]. Vestn Khir Im I I Grek (1997) 0.75
[The clinical variability of and approaches to treatment of life-threatening ventricular arrhythmias caused by SCN5A gene mutations]. Vestn Ross Akad Med Nauk (2007) 0.75
[Telemedicine technologies at the spacecrew landing site]. Aviakosm Ekolog Med (2013) 0.75
[Stargardt's disease and abiotrophy of Franceschetti (fundus flavimaculatus): pathogenetic, clinical, and molecular genetic characteristics]. Vestn Oftalmol (2014) 0.75
[Nozological spectrum of hereditary diseases of the nervous system in the cities of Volgograd and Volzhsky]. Genetika (2004) 0.75
[DNA-diagnosis of Emery-Dreifuss muscular dystrophy]. Zh Nevrol Psikhiatr Im S S Korsakova (2003) 0.75
[Immediate results of reconstructive surgery in end-stage dilated cardiomyopathy]. Vestn Khir Im I I Grek (2001) 0.75
[Clinic and genetic polymorphism of Brugada syndrome in Russian patients, caused by mutation in SCN5A gene]. Khirurgiia (Mosk) (2013) 0.75
[Lamine gene mutations in dilated cardiomyopathy]. Kardiologiia (2005) 0.75
[PROMISING OPTIONS FOR MEDICAL ROBOTICS APPLICATION IN SUPPORT OF CREW LIFE ACTIVITIES AND MITIGATION OF MEDICAL RISKS DURING SPACE FLIGHT]. Aviakosm Ekolog Med (2015) 0.75
[Experience of contemporary treatment of radiation burns in individuals subjected to ionizing radiation]. Med Tr Prom Ekol (2012) 0.75
[Genetic and epidemiologic analysis of hereditary diseases of the nervous system in the cities of Volgograd and Volzhskiĭ]. Genetika (2004) 0.75
[Clinical-genetic analysis of limb-girdle muscular dystrophy 2 type I]. Zh Nevrol Psikhiatr Im S S Korsakova (2012) 0.75
[Practical medico-genetic counseling for congenital and early loss of hearing in children]. Vestn Otorinolaringol (2008) 0.75
[Genetic structure of the Udmurt population]. Genetika (2007) 0.75
[Evaluation of the protective properties of nonwoven materials for throw-away medical overalls]. Gig Sanit (2006) 0.75
[Clinical-genetic characteristics of limb girdle-muscular dystrophy type 2A]. Zh Nevrol Psikhiatr Im S S Korsakova (2010) 0.75
[The preparation of latex diagnostic agents based on the surface antigens of Candida tropicalis]. Zh Mikrobiol Epidemiol Immunobiol (1995) 0.75
[Effect of hematopoietic and lymphoid cells on the stromal CFU colony formation in rabbit bone marrow cell cultures]. Gematol Transfuziol (1993) 0.75
[Dynamics of blood fibronectin and its correlation with the phenomenon of cryoglobulinemia in patients with ischemic stroke]. Zh Nevrol Psikhiatr Im S S Korsakova (2009) 0.75
[An effect of perindopril on the level of tumor necrosis factor-alpha and matrix metalloproteinase-9 in peripheral blood in the acute period of atherothrombotic ischemic stroke and myocardial infarction]. Zh Nevrol Psikhiatr Im S S Korsakova (2008) 0.75
[Experimental model of severe local radiation injuries of the skin after X-rays]. Patol Fiziol Eksp Ter (2014) 0.75
[Progress in genetic testing and prevention of hereditary hearing disorders]. Vestn Otorinolaringol (2007) 0.75
[Molecular analysis of the Y chromosome in XX sex-reversed patients]. Genetika (2008) 0.75
[Hereditary spastic paraplegia type 4 (SPG4): clinical and molecular-genetic characteristics]. Zh Nevrol Psikhiatr Im S S Korsakova (2010) 0.75
[Rigid spine congenital muscular dystrophy produced by SEPN1 mutations (RSMD1)]. Zh Nevrol Psikhiatr Im S S Korsakova (2014) 0.75
[Analysis of mutations and haplotypes of polymorphic markers in patients with Wilson-Konovalov disease from Bashkir]. Genetika (2000) 0.75
[Clinical-genetic correlations in the hereditary motor-sensor neuropathy caused by mutations in the MPZ (P0) gene]. Zh Nevrol Psikhiatr Im S S Korsakova (2011) 0.75
[Types of Y chromosome deletions and their frequency in infertile men]. Genetika (2006) 0.75
[Mutation analysis of K-ras protooncogene in colorectal adenocarcinomas and polyps in Russian patients]. Genetika (2010) 0.75
[Novel large deletion c.22-1320_633+1224del in the CYB5R3 gene from patients with hereditary methemoglobinemia]. Genetika (2012) 0.75
[The frequency and spectrum of mutations and the IVS8-T polymorphism of the CFTR gene in Russian infertile men]. Genetika (2010) 0.75
[Cell technologies in parodontology]. Stomatologiia (Mosk) (2009) 0.75
[Clinical and molecular genetic analysis of hereditary optic neuropathies]. Vestn Oftalmol (2013) 0.75
[Prospects for the use of cells possessing myogenic potential in the treatment of skeletal muscle diseases: a review of research. Part 1 - satellite cells]. Patol Fiziol Eksp Ter (2015) 0.75
[Comparison of different methods of molecular-genetic analysis of somatic mutations in K-ras gene in patients with colorectal cancer]. Vestn Ross Akad Med Nauk (2012) 0.75
[Mutation p.E92K is the primary cause of cystic fibrosis in Chuvashes]. Genetika (2012) 0.75
[Follicular cell (papillary and follicular) thyroid carcinoma, genetic inheritance, and molecular diagnostic markers]. Arkh Patol (2014) 0.75
[Distemper in a population of the Baikal seal]. Zh Mikrobiol Epidemiol Immunobiol (1990) 0.75
[Clinical-genetic characteristics of hereditary motor-sensory neuropathy type 1 X]. Zh Nevrol Psikhiatr Im S S Korsakova (2012) 0.75
[Crioglobulinemia in cerebral and coronal atherothrombosis]. Zh Nevrol Psikhiatr Im S S Korsakova (2005) 0.75
[Modern opportunities and prospects for studying pathogenesis, diagnosing and treating hereditary optic neuropathies]. Vestn Oftalmol (2015) 0.75
[Mesenchymal stem cells transplantation in the treatment of radiation skin lesions]. Patol Fiziol Eksp Ter (2011) 0.75
[Development of aids for monitoring the vital functions of cosmonauts' organism in extended space flight]. Aviakosm Ekolog Med (2013) 0.75
[Slow Formation and Degradation of γH2AX Foci in Human Skin Fibroblasts Exposed to Low-Dose X-Ray Radiation]. Radiats Biol Radioecol (2015) 0.75
[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan]. Genetika (2008) 0.75