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Internal Medicine (Tokyo, Japan)|November 12, 2023
Pathogenesis and Management of Citrin DeficiencyKiyoshi HayasakaJournal of Inherited Metabolic Disease|August 3, 2020
Metabolic basis and treatment of citrin deficiencyKiyoshi HayasakaJournal of Human Genetics|March 31, 2009
The GARS gene is rarely mutated in Japanese patients with Charcot-Marie-Tooth neuropathyAkiko Abe, Kiyoshi HayasakaNihon Rinsho. Japanese Journal of Clinical Medicine|March 11, 2014
[Congenital central hypoventilation syndrome: paradigm shifts and future prospects]Kiyoshi Hayasaka, Ayako SasakiNihon Rinsho. Japanese Journal of Clinical Medicine|March 16, 2011
[Genetic susceptibility to virus associated encephalitis or encephalopathy]Kazuyuki Nakamura, Kiyoshi HayasakaThe Application of Clinical Genetics|December 28, 2018
Adult-onset type II citrullinemia: Current insights and therapyKiyoshi Hayasaka, Chikahiko NumakuraBrain and Nerve = Shinkei Kenkyu No Shinpo|June 12, 2015
[Treatment and Pathomechanism of Citrin Deficiency]Kiyoshi Hayasaka, Chikahiko Numakura, Hisayoshi WatanabeNeuroscience Letters|January 23, 2009
Unusual circadian locomotor activity and pathophysiology in mutant CRY1 transgenic miceSatoshi Okano, Makoto Akashi, Kiyoshi Hayasaka, et al.Sleep and Biological Rhythms|July 22, 2016
Unique food-entrained circadian rhythm in cysteine414-alanine mutant mCRY1 transgenic miceSatoshi Okano, Akira Yasui, Kiyoshi Hayasaka, et al.Pediatric Neurology|May 4, 2005
Costello syndrome showing moyamoya-like vasculopathyTakashi Shiihara, Mitsuhiro Kato, Yoshihiko Mitsuhashi, et al.Pageof 11