K. Ohnari

发表

Electrophysiological Findings in Neuromyelitis Optica Spectrum Disorder

K. Ohnari, Hiroaki Adachi, 2021, Online Journal of Neurology and Brain Disorders.

Levels of nitric oxide metabolites in cerebrospinal fluid correlate with cognitive impairment in early stage multiple sclerosis

K. Okada, M. Tahara, Y. Sennari, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease

Y. Hayashi, Tomokatsu Yoshida, M. Nakagawa, 2013, Journal of Human Genetics.

An adult form of Alexander disease: a novel mutation in glial fibrillary acidic protein

S. Tsuji, T. Uozumi, M. Yamano, 2007, Journal of Neurology.

Assessment of the neurophysiologic examination in the earlier diagnosis of amyotrophic lateral sclerosis

S. Tsuji, T. Uozumi, A. Tamagawa, 2005 .

Unilateral positive–negative myoclonus in Creutzfeldt–Jakob disease

S. Tsuji, T. Uozumi, A. Tamagawa, 2006, Movement disorders : official journal of the Movement Disorder Society.

Severe symptoms of 16q-ADCA coexisting with SCA8 repeat expansion

S. Tsuji, T. Uozumi, K. Ohnari, 2008, Journal of the Neurological Sciences.

Late-onset Myasthenia Gravis Accompanied by Amyotrophic Lateral Sclerosis with Antibodies against the Acetylcholine Receptor and Low-density Lipoprotein Receptor-related Protein 4

H. Adachi, K. Okada, O. Higuchi, 2018, Internal medicine.

Glial fibrillary acidic protein mutations in adult‐onset Alexander disease: clinical features observed in 12 Japanese patients

Y. Hayashi, M. Nakagawa, I. Mizuta, 2011, Acta neurologica Scandinavica.

Evoked potentials are useful for diagnosis of neuromyelitis optica spectrum disorder

H. Adachi, K. Okada, Toshiyuki Takahashi, 2016, Journal of the Neurological Sciences.

Unclassified subtype of Guillain-Barré syndrome is associated with quick recovery

S. Kusunoki, H. Adachi, K. Okada, 2021, Journal of Clinical Neuroscience.