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O Onodera

Showing results (71-80 of 92) with videos related to

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Neurology|January 5, 2002
Paraneoplastic striatal encephalitisT Oguma, H Kobayashi, S Katada, et al.
Neurology|April 13, 2011
A novel mutation in the HTRA1 gene causes CARASIL without alopeciaY Nishimoto, M Shibata, M Nihonmatsu, et al.
Annals of Neurology|August 1, 1996
Lack of association of very low density lipoprotein receptor gene polymorphism with Caucasian Alzheimer's diseaseK Okuizumi, O Onodera, K Seki, et al.
European Journal of Neurology|September 19, 2017
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutationT Konno, K Yoshida, I Mizuta, et al.
European Journal of Neurology|September 30, 2016
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutationT Konno, K Yoshida, T Mizuno, et al.
Neurology|June 27, 2008
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 familiesK Hara, A Shiga, H Nozaki, et al.
Journal of Medical Genetics|August 7, 2007
Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in AsiaN Maksimova, K Hara, A Miyashia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 18, 2009
Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer diseaseK Kasuga, T Shimohata, A Nishimura, et al.
Annals of Neurology|October 1, 1994
Trinucleotide repeat length and rate of progression of Huntington's diseaseS N Illarioshkin, S Igarashi, O Onodera, et al.
Annals of Neurology|March 20, 1998
Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph diseaseO Onodera, J Idezuka, S Igarashi, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Neurology|January 5, 2002
Paraneoplastic striatal encephalitisT Oguma, H Kobayashi, S Katada, et al.
Neurology|April 13, 2011
A novel mutation in the HTRA1 gene causes CARASIL without alopeciaY Nishimoto, M Shibata, M Nihonmatsu, et al.
Annals of Neurology|August 1, 1996
Lack of association of very low density lipoprotein receptor gene polymorphism with Caucasian Alzheimer's diseaseK Okuizumi, O Onodera, K Seki, et al.
European Journal of Neurology|September 19, 2017
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutationT Konno, K Yoshida, I Mizuta, et al.
European Journal of Neurology|September 30, 2016
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutationT Konno, K Yoshida, T Mizuno, et al.
Neurology|June 27, 2008
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 familiesK Hara, A Shiga, H Nozaki, et al.
Journal of Medical Genetics|August 7, 2007
Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in AsiaN Maksimova, K Hara, A Miyashia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 18, 2009
Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer diseaseK Kasuga, T Shimohata, A Nishimura, et al.
Annals of Neurology|October 1, 1994
Trinucleotide repeat length and rate of progression of Huntington's diseaseS N Illarioshkin, S Igarashi, O Onodera, et al.
Annals of Neurology|March 20, 1998
Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph diseaseO Onodera, J Idezuka, S Igarashi, et al.
Pageof 10