Kiyoshi Hayasaka

Emeritus and visiting Professor,

Yamagata University Faculty of Medicine

Japan

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About

Professor Kiyoshi Hayasaka is an Emeritus and visiting Professor at Yamagata University School of Medicine, Japan. His research focuses on the pathogenesis and management of metabolic disorders, as illustrated in his recent articles on citrin deficiency and glutaric aciduria type 1. Additionally, he has contributed to the understanding of genetic variants associated with biliary tract anomalies and inherited bleeding diathesis.

Articles (12)

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2025

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2024

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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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2020

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2020

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2020

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2020

Collaborators (4)

Yoriko Watanabe

Professor

Kurume University School of Medicine

JAPAN

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Hiroshi Doi

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

Yokohama National University

JAPAN

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Kazuharu Misawa

Associate Professor

Yokohama National University

JAPAN

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Eriko Koshimizu

Yokohama City University Graduate School of Medicine

JAPAN

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Kiyoshi Hayasaka

Research Interests

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Articles (12)

Colorectal cancer in a patient with glutaric aciduria type 1

Pathogenesis and Management of Citrin Deficiency

Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencing.

Heterozygous calcyclin-binding protein/Siah1-interacting protein (CACYBP/SIP) gene pathogenic variant linked to a dominant family with paucity of interlobular bile duct

Heterozygous calcyclin-binding protein/Siah1-interacting protein (CACYBP/SIP) gene pathogenic variant linked to a dominant family with paucity of interlobular bile duct

ALOX12 mutation in a family with dominantly inherited bleeding diathesis

ALOX12 mutation in a family with dominantly inherited bleeding diathesis

Metabolic basis and treatment of citrin deficiency

Diabetes mellitus exacerbates citrin deficiency via glucose toxicity

Metabolic basis and treatment of citrin deficiency

Adult cases of late-onset congenital central hypoventilation syndrome and paired-like homeobox 2B-mutation carriers: an additional case report and pooled analysis

Adult cases of late-onset congenital central hypoventilation syndrome and paired-like homeobox 2B-mutation carriers: an additional case report and pooled analysis

Collaborators (4)

Yoriko Watanabe

Hiroshi Doi

Kazuharu Misawa

Eriko Koshimizu

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