S. Kotorii

Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis

T. Tabira, E. Uyama, D. Chui, 2003, Journal of the Neurological Sciences.

Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASIL.

T. Tabira, M. Uchino, E. Uyama, 2000, Internal medicine.

Mutations of the Notch3 Gene in Non-Caucasian Patients with Suspected CADASIL Syndrome

K. Arima, G. Kuchel, T. Tabira, 2001, Dementia and Geriatric Cognitive Disorders.

Notch3 gene in CADASIL syndrome: mutation frequencies in Japanese and its expression and processing

T. Tabira, D. Chui, K. Shirotani, 2001 .

CDR3 Spectratyping Analysis of the TCR Repertoire in Myasthenia Gravis1

K. Kohyama, Y. Matsumoto, T. Kondo, 2006, The Journal of Immunology.

Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

T. Tabira, M. Uchino, E. Uyama, 1999, Alzheimer disease and associated disorders.

[Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].

T. Tabira, Y. Sunada, K. Takahashi, 2001, Rinsho shinkeigaku = Clinical neurology.