Masashi Aoki

Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis

Fumiaki Tanaka, Gen Sobue, Akiko Tamakoshi, 2009, Journal of the Neurological Sciences.

A novel two-base mutation in the CuZn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in Japan

Yasuto Itoyama, Koji Abe, Takafumi Hasegawa, 1996, Neuroscience Letters.

Confirmatory double-blind, parallel-group, placebo-controlled study of efficacy and safety of edaravone (MCI-186) in amyotrophic lateral sclerosis patients

Yasuto Itoyama, Koji Abe, Chikuma Hamada, 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Earlier tachycardia onset in right than left mesial temporal lobe seizures

Nobukazu Nakasato, Yosuke Kakisaka, Masaki Iwasaki, 2014, Neurology.

Severe olfactory dysfunction is a prodromal symptom of dementia associated with Parkinson's disease: a 3 year longitudinal study.

Hiroshi Fukuda, Yasuto Itoyama, Kazumi Hirayama, 2012, Brain : a journal of neurology.

Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome

Koichi Tabayashi, Kenji Kurosawa, Yoichi Matsubara, 2008, Journal of Human Genetics.

Gender difference in association between polymorphism of serotonin transporter gene regulatory region and anxiety.

Yasuto Itoyama, Atsushi Utsumi, Masahiro Hiratsuka, 2006, Journal of psychosomatic research.

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Pieter J. de Jong, Saeed Bohlega, Jing Liu, 1998, Nature Genetics.