Koyama, Akihide

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease

Hara, K., Shiga, A., Fukutake, T., Nozaki, H., Miyashita, A., Yokoseki, A., Kawata, H., Koyama, A., Arima, K., Takahashi, T., et al. (2009) · New England Journal of Medicine

Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments

Cited by 460

TDP ‐ 43 mutation in familial amyotrophic lateral sclerosis

Yokoseki, A., Shiga, A., Tan, C., Tagawa, A., Kaneko, H., Koyama, A., Eguchi, H., Tsujino, A., Ikeuchi, T., Kakita, A., et al. (2008) · Annals of Neurology

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 373

ApoE-isoform-dependent cellular uptake of amyloid-β is mediated by lipoprotein receptor LR11/SorLA

Yajima, R., Tokutake, T., Koyama, A., Kasuga, K., Tezuka, T., Nishizawa, M., & Ikeuchi, T. (2015) · Biochemical and Biophysical Research Communications

Alzheimer's disease research and treatmentsCellular transport and secretion

Cited by 43

Adrenomyeloneuropathy: Report of a family and electron microscopical findings in peripheral nerve

Tanaka, K., Koyama, A., Koike, R., Ohno, T., Atsumi, T., & Miyatake, T. (1985) · Journal of Neurology

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 18