I. Yoshimura

Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy

M. T. Medina, K. Yamakawa, S. Fujimoto, 2008, Neurology.

Juvenile Parkinson's disease with widespread Lewy bodies in the brain

S. Hayashi, I. Yoshimura, N. Yoshimura, 2004, Acta Neuropathologica.

[A case of congenital myotonic dystrophy with infantile autism].

I. Yoshimura, H. Akimoto, N. Yoshimura, 1989, No to hattatsu = Brain and development.

Long-term observations of two siblings with Lafora disease treated with zonisamide

S. Kaneko, I. Yoshimura, N. Yoshimura, 2001, Epilepsy Research.

Co‐localization of β‐peptide and phosphorylated tau in astrocytes in a patient with corticobasal degeneration

M. Hasegawa, Hitoshi Takahashi, K. Wakabayashi, 2006, Neuropathology : official journal of the Japanese Society of Neuropathology.

juvenile myoclonic epilepsy in sporadic and familial Myoclonin 1 / EFHC 1 Novel mutations in

M. T. Medina, K. Yamakawa, S. Fujimoto, 2008 .