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1,734 results
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Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems.
Tada M, Nishizawa M, Onodera O. Tada M, et al. J Neurol Neurosurg Psychiatry. 2015 Aug;86(8):922-8. doi: 10.1136/jnnp-2013-307225. Epub 2015 Jan 30. J Neurol Neurosurg Psychiatry. 2015. PMID: 25637456 Review.
Babinski-Nageotte syndrome with ipsilateral hemiparesis.
Tada M, Tada M, Ishiguro H, Hirota K. Tada M, et al. Arch Neurol. 2005 Apr;62(4):676-7. doi: 10.1001/archneur.62.4.676. Arch Neurol. 2005. PMID: 15824273 No abstract available.
Early development of autonomic dysfunction may predict poor prognosis in patients with multiple system atrophy.
Tada M, Onodera O, Tada M, Ozawa T, Piao YS, Kakita A, Takahashi H, Nishizawa M. Tada M, et al. Arch Neurol. 2007 Feb;64(2):256-60. doi: 10.1001/archneur.64.2.256. Arch Neurol. 2007. PMID: 17296842
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1.
Tada M, Yokoseki A, Sato T, Makifuchi T, Onodera O. Tada M, et al. Adv Exp Med Biol. 2010;685:21-33. doi: 10.1007/978-1-4419-6448-9_3. Adv Exp Med Biol. 2010. PMID: 20687492 Review.
Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia.
Yokoseki A, Ishihara T, Koyama A, Shiga A, Yamada M, Suzuki C, Sekijima Y, Maruta K, Tsuchiya M, Date H, Sato T, Tada M, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O. Yokoseki A, et al. Among authors: tada m. Brain. 2011 May;134(Pt 5):1387-99. doi: 10.1093/brain/awr069. Epub 2011 Apr 12. Brain. 2011. PMID: 21486904
Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS.
Konno T, Tada M, Tada M, Koyama A, Nozaki H, Harigaya Y, Nishimiya J, Matsunaga A, Yoshikura N, Ishihara K, Arakawa M, Isami A, Okazaki K, Yokoo H, Itoh K, Yoneda M, Kawamura M, Inuzuka T, Takahashi H, Nishizawa M, Onodera O, Kakita A, Ikeuchi T. Konno T, et al. Among authors: tada m, tada m. Neurology. 2014 Jan 14;82(2):139-48. doi: 10.1212/WNL.0000000000000046. Epub 2013 Dec 13. Neurology. 2014. PMID: 24336230 Free PMC article.
[Disease notification and self-determination in treatment decisions for patients with Creutzfeldt-Jakob disease].
Yanagimura F, Shimohata T, Tada M, Nozaki H, Nishizawa M. Yanagimura F, et al. Among authors: tada m. Rinsho Shinkeigaku. 2014;54(4):298-302. doi: 10.5692/clinicalneurol.54.298. Rinsho Shinkeigaku. 2014. PMID: 24807271 Japanese.
Roles of inositol 1,4,5-trisphosphate receptors in spinocerebellar ataxias.
Tada M, Nishizawa M, Onodera O. Tada M, et al. Neurochem Int. 2016 Mar;94:1-8. doi: 10.1016/j.neuint.2016.01.007. Epub 2016 Jan 28. Neurochem Int. 2016. PMID: 26827887 Review.
Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids.
Tada M, Konno T, Tada M, Tezuka T, Miura T, Mezaki N, Okazaki K, Arakawa M, Itoh K, Yamamoto T, Yokoo H, Yoshikura N, Ishihara K, Horie M, Takebayashi H, Toyoshima Y, Naito M, Onodera O, Nishizawa M, Takahashi H, Ikeuchi T, Kakita A. Tada M, et al. Ann Neurol. 2016 Oct;80(4):554-65. doi: 10.1002/ana.24754. Epub 2016 Sep 4. Ann Neurol. 2016. PMID: 27490250
[Overview of Hereditary Spinocerebellar Ataxias in Japan].
Tada M, Yokoseki A, Onodera O. Tada M, et al. Brain Nerve. 2017 Aug;69(8):879-890. doi: 10.11477/mf.1416200839. Brain Nerve. 2017. PMID: 28819072 Japanese.
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