S. Tsuneishi

Mutation analysis of the ornithine transcarbamylase (OTC) gene in five Japanese OTC deficiency patients revealed two known and three novel mutations including a deep intronic mutation.

Y. Takeshima, M. Matsuo, K. Saiki, 2007, The Kobe journal of medical sciences.

Application of a wearable switch to perform a mouse left click for a child with mix type of cerebral palsy: a single case study

M. Yagi, S. Tsuneishi, S. Takada, 2020, Disability and rehabilitation. Assistive technology.

Effect of CPS14217C>A genotype on valproic‐acid‐induced hyperammonemia

M. Matsuo, T. Sakaeda, K. Okumura, 2010, Pediatrics international : official journal of the Japan Pediatric Society.

Genotype–phenotype correlations in alternating hemiplegia of childhood

Akihiro Yasuhara, Hirokazu Oguni, Bo Zhang, 2014, Neurology.

Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia

H. Kurahashi, H. Nishio, N. Okamoto, 2018, Clinical genetics.

Combination Effect of Systemic Hypothermia and Caspase Inhibitor Administration against Hypoxic-Ischemic Brain Damage in Neonatal Rats

S. Tsuneishi, Hajime Nakamura, S. Takada, 2001, Pediatric Research.