日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Lateral Tension Upper Body Lift: "Zip-Shark" Technique as Novel Procedure

侧向张力上身提升术:“拉链鲨”技术作为一种新型手术方法

Sharkov, Evgeni Vanyov; Sharkova, Irina Georgieva; Simeonov, Dimitar Plamenov

Cardiovascular Functioning Features in Individuals with Connective Tissue Dysplasia Engaged in Sports for the Disabled

患有结缔组织发育不良症并参与残疾人运动的个体的心血管功能特征

Vinokurova, Kamiliia; Zakharova, Anna; Zinovieva, Yulia; Epifanov, Arseniy; Galdobina, Anna; Sharkova, Ekaterina; Blyakhman, Felix

A Spectrum of Pathogenic Variants in the LAMA2 Gene in the Russian Federation

俄罗斯联邦LAMA2基因致病变异谱

Chausova, Polina; Cherevatova, Tatiana; Dadali, Elena; Murtazina, Aysylu; Bulakh, Maria; Kurbatov, Sergei; Anisimova, Inga; Kanivets, Ilya; Udalova, Vasilisa; Rudenskaya, Galina; Demina, Nina; Sharkova, Inna; Monakhova, Anastasia; Tsygankova, Polina; Markova, Tatiana; Ryzhkova, Oksana; Shatohina, Olga; Galkina, Varvara; Borovikov, Artem; Mishina, Irina; Shchagina, Olga; Chukhrova, Alena; Polyakov, Aleksander

Balanced Translocations Involving the DMD Gene as a Cause of Muscular Dystrophy in Female Children: A Description of Three Cases

涉及DMD基因的平衡易位是导致女性儿童肌营养不良症的原因:三例病例报告

Vorontsova, Ekaterina O; Murtazina, Aysylu; Zinina, Elena; Polyakov, Alexander V; Sumina, Maria; Rybakova, Olga A; Vlodavets, Dmitry; Kazakov, Dmitry; Suvorova, Yulia; Sharkova, Inna V; Demina, Nina A; Repina, Svetlana A; Bulanova, Vera A; Antonova, Maria; Dadali, Elena; Marakhonov, Andrey V; Shilova, Nadezhda V; Kutsev, Sergey I; Shchagina, Olga A

Photoreceptor calyceal processes accompany the developing outer segment, adopting a stable length despite a dynamic core

感光体萼突伴随外节的发育,尽管核心处于动态变化中,但其长度却保持稳定

Maria Sharkova, Gonzalo Aparicio, Constantin Mouzaaber, Flavio R Zolessi, Jennifer C Hocking

Mild phenotype of CHAT-associated congenital myasthenic syndrome: case series

CHAT相关先天性肌无力综合征的轻型表型:病例系列

Murtazina, Aysylu; Borovikov, Artem; Marakhonov, Andrey; Sharkov, Artem; Sharkova, Inna; Mirzoyan, Alena; Kulikova, Sviatlana; Ganieva, Ralina; Zabnenkova, Viktoriia; Ryzhkova, Oksana; Nikitin, Sergey; Dadali, Elena; Kutsev, Sergey

Case Report: Exploring the clinical spectrum of LGMD R27: insights from a case study with homozygous pathogenic variant in the JAG2 gene

病例报告:探索 LGMD R27 的临床谱:来自 JAG2 基因纯合致病变异病例研究的启示

Nikitin, Sergey; Melnik, Evgeniya; Sharkova, Inna; Murtazina, Aysylu; Shchagina, Olga; Zabnenkova, Victoriia; Tsargush, Vadim; Dadali, Elena; Kutsev, Sergey

TRA2B Gene Splice Variant Linked to Seizures and Neurodevelopmental Delay: A Second Case Study

TRA2B基因剪接变异与癫痫和神经发育迟缓相关:第二个病例研究

Shatokhina, Olga; Kovalskaia, Valeriia; Sparber, Peter; Sharkova, Inna; Mishina, Irina; Kuznetsova, Vera; Ryzhkova, Oxana

The morphological and functional diversity of apical microvilli

顶端微绒毛的形态和功能多样性

Sharkova, Maria; Chow, Erica; Erickson, Timothy; Hocking, Jennifer C

Case report: Unusual episodic myopathy in a patient with novel homozygous deletion of first coding exon of MICU1 gene

病例报告:MICU1基因第一个编码外显子新发纯合缺失患者出现罕见发作性肌病

Sharova, Margarita; Skoblov, Mikhail; Dadali, Elena; Demina, Nina; Shchagina, Olga; Konovalov, Fedor; Ampleeva, Maria; Sharkova, Inna; Kutsev, Sergey