S
Satoshi Kotorii
Publications - 9
Citations - 228
Satoshi Kotorii is an academic researcher. The author has contributed to research in topics: CADASIL & Leukoencephalopathy. The author has an hindex of 7, co-authored 9 publications receiving 226 citations.
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Journal ArticleDOI
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.
Yo Santa,Eiichiro Uyama,De Hua Chui,Masakuni Arima,Satoshi Kotorii,Keikichi Takahashi,Takeshi Tabira +6 more
TL;DR: Examination of Notch3 mutations in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy suggests that hemodynamic abnormalities due to smooth muscle cell degeneration may be important in the pathogenesis of CADASIL.
Journal ArticleDOI
CDR3 spectratyping analysis of the TCR repertoire in myasthenia gravis.
Yoh Matsumoto,Hidenori Matsuo,Hiroshi Sakuma,Il-Kwon Park,Yukiko Tsukada,Kuniko Kohyama,Takayuki Kondo,Satoshi Kotorii,Noritoshi Shibuya +8 more
TL;DR: Large-scale cross-sectional and longitudinal TCR studies by CDR3 spectratyping using PBL and thymus tissues from MG patients suggest that persistent clonal expansions of T cells in MG patients are associated with the development and maintenance of MG.
Journal ArticleDOI
Mutations of the Notch3 Gene in Non-Caucasian Patients with Suspected CADASIL Syndrome
Satoshi Kotorii,Keikichi Takahashi,Kohei Kamimura,Takeshi Nishio,Kunimasa Arima,Haruki Yamada,Eiichiro Uyama,Makoto Uchino,Akihito Suenaga,Masayasu Matsumoto,George A. Kuchel,Guy A. Rouleau,Takeshi Tabira +12 more
TL;DR: The Notch3 gene has been recently identified as a causative gene for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) as mentioned in this paper.
Journal ArticleDOI
Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Kohei Kamimura,Keikichi Takahashi,Eiichiro Uyama,Makoto Tokunaga,Satoshi Kotorii,Makoto Uchino,Takeshi Tabira +6 more
TL;DR: The Notch3 gene is determined in a Japanese family with CADASIL symptoms and found a missense mutation (Arg133Cys) in exon 4 that was heterozygous and cosegregated with the disease.
Journal Article
[Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].
Haruki Yamada,Takeshi Yasuda,Satoshi Kotorii,Keikichi Takahashi,Takeshi Tabira,Yoshihide Sunada +5 more
TL;DR: The clinical symptoms, the family history and the MRI findings suggested the diagnosis of CADASIL, but the patient also showed alopecia and lumbar herniated disk, both are characteristic features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).