Takeshi Yoshida

助教 / Assistant Professor

Kyoto University

Japan

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About

Takeshi Yoshida is an Assistant Professor at Kyoto University in Japan. His research focuses on fields including neurological disorders, muscular dystrophies, and genetic analyses of rare diseases. Recent articles authored by Professor Yoshida investigate various topics such as biomarkers for epileptic encephalopathy and the genetic basis of muscular dystrophy, contributing to advancements in understanding complex medical conditions.

Articles (19)

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JAPAN

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Kyoichi Tomoto

The Jikei University Hospital

JAPAN

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Satoshi Kodama

University of Tokyo Hospital

JAPAN

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Dai Watanabe

Kyoto Prefectural University of Medicine

JAPAN

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Kouji Harada

Associate Professor

Kyoto University

JAPAN

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Kentaro Tokumoto

Shizuoka Kenritsu Shizuoka Gan Center

JAPAN

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Takeshi Yoshida

Research Interests

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Articles (19)

MicroRNA-33 inhibition ameliorates muscular dystrophy by enhancing skeletal muscle regeneration

Morphological erythrocyte abnormalities as potential biomarker of uridine-responsive epileptic encephalopathy

Atrioventricular Block in a Pompe Disease Patient Receiving Enzyme Replacement Therapy

Aberrant lysosomal dynamics disrupt myogenesis via mTORC1 signalling in X-linked myotubular myopathy

Glycosylphosphatidylinositol Biosynthesis Defect Due To Novel Biallelic Pathogenic Variants in PIGW

Prolonged Febrile Seizure and Long‐Term Neurological Sequelae in Otherwise Healthy Children

Genetic Analysis of SCN11A, SCN10A, and SCN9A in Familial Episodic Pain Syndrome (FEPS) in Japan and Proposal of Clinical Diagnostic Criteria

Exploring unsolved cases of lissencephaly spectrum: integrating exome and genome sequencing for higher diagnostic yield

A mild case of Cockayne syndrome with a novel start-loss variant of ERCC8

Long-read sequencing identifies an SVA_D retrotransposon insertion deep within the intron of ATP7A as a novel cause of occipital horn syndrome

Successful sequential therapy with rituximab and daratumumab for refractory posttransplant immune thrombocytopenic purpura

Leigh-like syndrome with progressive cerebellar atrophy caused by novel HIBCH variants

A case of congenital myopathy accompanied by tremor due to a MYBPC1 mutation

Risk factors for psychological distress in electroencephalography technicians during the COVID-19 pandemic: A national-level cross-sectional survey in Japan

Isolated sixth nerve palsy as an initial presentation of primary angiitis of the central nervous system

Efficacy of long‐term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case series

Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants

Gait improvements by assisting hip movements with the robot in children with cerebral palsy: a pilot randomized controlled trial.

Acute Flaccid Myelitis With Neuroradiological Finding of Brachial Plexus Swelling

Collaborators (10)

Takahiro Horie

Tomohide Takaya

Hatasu Kobayashi

Katsutsugu Umeda

Atsuko Noguchi

Kyoichi Tomoto

Satoshi Kodama

Dai Watanabe

Kouji Harada

Kentaro Tokumoto

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