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Dynamic Modes of Current-Carrying Elements of REBCO Tapes with no Copper Stabilizer at 77 and 4.2 K

Physics of atomic nuclei, 2022-12, Vol.85 (7), p.1154-1161

2022

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Tract-Based Spatial Statistical Analysis of Diffusion Tensor Imaging in Pediatric Patients with Mitochondrial Disease: Widespread Reduction in Fractional Anisotropy of White Matter Tracts

American journal of neuroradiology : AJNR, 2012-10, Vol.33 (9), p.1726-1730

2012

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Myotonia and myotonic discharges of dystrophic myotonia type 1 at the first decade onset: a literature review and data of the case series

Nervno-myshechnye bolezni, 2022-06, Vol.12 (2), p.47-63

2022

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On Detection of Narrow Angle \!+\!- Pairs From Dark Photon Decays

IEEE transactions on nuclear science, 2015-12, Vol.62 (6), p.3283-3287

2015

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Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in GNRHR genes

Problemy ėndokrinologii, 2021-05, Vol.67 (3), p.62-67

2021

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Diagnostic utility of exome sequencing for inherited peripheral neuropathies

Nervno-myshechnye bolezni, 2020-12, Vol.10 (4), p.12-26

2020

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Stretch reflexes in human masseter

The Journal of physiology, 1994-04, Vol.476 (2), p.323-331

1994

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Functional identification of the input-output transforms of motoneurones in the rat and cat

The Journal of physiology, 1997-10, Vol.504 (Pt 2), p.401-424

1997

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The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances

Vestnik otorinolaringologii, 2014 (2), p.37

2014

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PROMISING OPTIONS FOR MEDICAL ROBOTICS APPLICATION IN SUPPORT OF CREW LIFE ACTIVITIES AND MITIGATION OF MEDICAL RISKS DURING SPACE FLIGHT

Aviakosmicheskaia i Äkologicheskaia meditsina, 2015, Vol.49 (6), p.76-83

2015

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Responses of human masseter motor units to stretch

The Journal of physiology, 1995-02, Vol.483 (Pt 1), p.251-264

1995

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Partial Inactivation of the Primary Motor Cortex Hand Area: Effects on Individuated Finger Movements

The Journal of neuroscience, 1998-11, Vol.18 (21), p.9038-9054

1998

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Effects of background noise on the response of rat and cat motoneurones to excitatory current transients

The Journal of physiology, 1996-08, Vol.495 (Pt 1), p.143-157

1996

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The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns

Genetika, 2014-02, Vol.50 (2), p.214

2014

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New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance

Genetika, 2014-04, Vol.50 (4), p.474

2014

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Limited Functional Grouping of Neurons in the Motor Cortex Hand Area During Individuated Finger Movements: A Cluster Analysis

Journal of neurophysiology, 1999-12, Vol.82 (6), p.3488-3505

1999

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Development of aids for monitoring the vital functions of cosmonauts' organism in extended space flight

Aviakosmicheskaia i Äkologicheskaia meditsina, 2013-05, Vol.47 (3), p.62-63

2013

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Multiple fragment statistical analysis of post-spike effects in spike-triggered averages of rectified EMG

Journal of neuroscience methods, 1998-02, Vol.79 (2), p.143-150

1998

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Genome of the Western Clawed Frog Xenopus tropicalis

Science (American Association for the Advancement of Science), 2010-04, Vol.328 (5978), p.633-636

2010

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Population frequency and age of c.806C > T mutation in CYB5R3 gene as cause of recessive congenital methemoglobinemia in Yakutia

Genetika, 2013-04, Vol.49 (4), p.523

2013

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Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness

Genetika, 2012-01, Vol.48 (1), p.112

2012

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Construction features and environmental factors influencing corrosion on a self-contained fluid-filled submarine cable circuit in Long Island Sound

IEEE transactions on power delivery, 1998-07, Vol.13 (3), p.677-682

1998

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Stargardt's disease and abiotrophy of Franceschetti (fundus flavimaculatus): pathogenetic, clinical, and molecular genetic characteristics

Vestnik oftal'mologii, 2014-03, Vol.130 (2), p.72

2014

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Heterozygous carrier rate for type I-IV proximal spinal muscular atrophy in Chuvashes, Udmurts, and residents of the Moscow region

Genetika, 2012-08, Vol.48 (8), p.983

2012

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Fingerprint Identification using Spherical Local-Sensitive Hashing

PROGRAMMNAYA INGENERIA, 2017-05, Vol.8 (5), p.207-214

Poliakov, A. V.

2017

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Dynamic Modes of Current-Carrying Elements of REBCO Tapes with no Copper Stabilizer at 77 and 4.2 K

Tract-Based Spatial Statistical Analysis of Diffusion Tensor Imaging in Pediatric Patients with Mitochondrial Disease: Widespread Reduction in Fractional Anisotropy of White Matter Tracts

Myotonia and myotonic discharges of dystrophic myotonia type 1 at the first decade onset: a literature review and data of the case series

On Detection of Narrow Angle \!+\!- Pairs From Dark Photon Decays

Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in GNRHR genes

Diagnostic utility of exome sequencing for inherited peripheral neuropathies

Stretch reflexes in human masseter

Functional identification of the input-output transforms of motoneurones in the rat and cat

The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances

PROMISING OPTIONS FOR MEDICAL ROBOTICS APPLICATION IN SUPPORT OF CREW LIFE ACTIVITIES AND MITIGATION OF MEDICAL RISKS DURING SPACE FLIGHT

Responses of human masseter motor units to stretch

Partial Inactivation of the Primary Motor Cortex Hand Area: Effects on Individuated Finger Movements

Effects of background noise on the response of rat and cat motoneurones to excitatory current transients

The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns

New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance

Limited Functional Grouping of Neurons in the Motor Cortex Hand Area During Individuated Finger Movements: A Cluster Analysis

Development of aids for monitoring the vital functions of cosmonauts' organism in extended space flight

Multiple fragment statistical analysis of post-spike effects in spike-triggered averages of rectified EMG

Genome of the Western Clawed Frog Xenopus tropicalis

Population frequency and age of c.806C > T mutation in CYB5R3 gene as cause of recessive congenital methemoglobinemia in Yakutia

Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness

Construction features and environmental factors influencing corrosion on a self-contained fluid-filled submarine cable circuit in Long Island Sound

Stargardt's disease and abiotrophy of Franceschetti (fundus flavimaculatus): pathogenetic, clinical, and molecular genetic characteristics

Heterozygous carrier rate for type I-IV proximal spinal muscular atrophy in Chuvashes, Udmurts, and residents of the Moscow region

Fingerprint Identification using Spherical Local-Sensitive Hashing

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