Mitsuhiro Kato

Professor

Showa University

Japan

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Articles (12)

Year:

2024

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2024

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

Collaborators (17)

Chiaki Ohtaka-Maruyama

Tokyo Metropolitan Institute of Medical Science

JAPAN

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Takuma Kumamoto

Tokyo Metropolitan Institute of Medical Science

JAPAN

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Hiroshi Doi

Associate professor/M.D., Ph.D.

Yokohama National University

JAPAN

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Tenpei Akita

Professor

Hamamatsu Ika Daigaku

JAPAN

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Hirotomo Saitsu

Hamamatsu University School of Medicine

JAPAN

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Takeshi Mizuguchi

Associate Professor

Yokohama National University

JAPAN

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Elsa Leitão

Universitätsklinikum Essen Institut für Humangenetik

GERMANY

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Hiroki Hoshino

Tohoku University Hospital

JAPAN

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Hideaki Kanemura

JAPAN

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Naomi Tsuchida

Yokohama City University Medical Center

JAPAN

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Yuri Uchiyama

Assistant professor

Yokohama City University Medical Center

JAPAN

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Naomichi Matsumoto

Professor and Chair

Yokohama City University Graduate School of Medicine

JAPAN

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Fuyuki Miya

Associate Professor

Keio University

JAPAN

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Kazuharu Misawa

Associate Professor

Yokohama National University

JAPAN

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Hideyuki Takeuchi

Associate Professor

Yokohama National University

JAPAN

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Takaaki Matsui

Associate Professor

Nara Institute of Science and Technology（NAIST）

JAPAN

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Eriko Koshimizu

Yokohama City University Graduate School of Medicine

JAPAN

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Mitsuhiro Kato

Research Interests

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Articles (12)

Detection of hidden intronic DDC variant in aromatic L-amino acid decarboxylase deficiency by adaptive sampling

Splicing variant of WDR37 in a case of Neurooculocardiogenitourinary syndrome

Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies

De novo CLCN3 variants affecting Gly327 cause severe neurodevelopmental syndrome with brain structural abnormalities

A novel de novo KCNB1 variant altering channel characteristics in a patient with periventricular heterotopia, abnormal corpus callosum, and mild seizure outcome

A New Case With Cortical Malformation Caused by Biallelic Variants in LAMC3

Sirolimus for epileptic seizures associated with focal cortical dysplasia type II

Efficacy of ethosuximide on atonic seizures with KCNB1 mutation

De novo ATP1A3 variants cause polymicrogyria

A boy with biallelic frameshift variants in TTC5 and brain malformation resembling tubulinopathies

Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

ATP6V0A1 encoding the a1-subunit of the V0 domain of vacuolar H+-ATPases is essential for brain development in humans and mice

Collaborators (17)

Chiaki Ohtaka-Maruyama

Takuma Kumamoto

Hiroshi Doi

Tenpei Akita

Hirotomo Saitsu

Takeshi Mizuguchi

Elsa Leitão

Hiroki Hoshino

Hideaki Kanemura

Naomi Tsuchida

Yuri Uchiyama

Naomichi Matsumoto

Fuyuki Miya

Kazuharu Misawa

Hideyuki Takeuchi

Takaaki Matsui

Eriko Koshimizu

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