Eiichiro Uyama, MD

Affiliations: 
Neurology Kumamoto University, Kumamoto-shi, Kumamoto-ken, Japan 
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"Eiichiro Uyama"
Bio:

http://onlinelibrary.wiley.com/doi/10.1002/1097-4598(200010)23:10%3C1549::AID-MUS11%3E3.0.CO;2-0/abstract

http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0404.1994.tb01657.x/abstract
http://pubget.com/profile/author/Eiichiro%20Uyama
http://en.scientificcommons.org/eiichiro_uyama

Mean distance: 19.07 (cluster 24)
 
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Publications

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Ueda A, Ueda M, Nagatoshi A, et al. (2015) Genotypic and phenotypic spectrum of CADASIL in Japan: the experience at a referral center in Kumamoto University from 1997 to 2014. Journal of Neurology
Nakahara K, Ueda M, Yamada K, et al. (2014) Juvenile-onset parkinsonism with digenic parkin and PINK1 mutations treated with subthalamic nucleus stimulation at 45 years after disease onset. Journal of the Neurological Sciences. 345: 276-7
Funayama M, Li Y, Tsoi TH, et al. (2008) Familial Parkinsonism with digenic parkin and PINK1 mutations. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 1461-5
Yamada K, Andrews C, Chan WM, et al. (2003) Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). Nature Genetics. 35: 318-21
Arai A, Tanaka K, Ikeuchi T, et al. (2002) A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees. Annals of Neurology. 52: 516-9
Sasaki R, Ito N, Shimamura M, et al. (2001) A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenita. Muscle & Nerve. 24: 357-63
Sasaki R, Ichiyasu H, Ito N, et al. (1999) Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia. Neuromuscular Disorders : Nmd. 9: 587-92
Yoshida K, Oshima A, Sakuraba H, et al. (1992) GM1 gangliosidosis in adults: clinical and molecular analysis of 16 Japanese patients. Annals of Neurology. 31: 328-32
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