Tada M - Search Results

1

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.

Stevanin G, Azzedine H, Denora P, Boukhris A, Tazir M, Lossos A, Rosa AL, Lerer I, Hamri A, Alegria P, Loureiro J, Tada M, Hannequin D, Anheim M, Goizet C, Gonzalez-Martinez V, Le Ber I, Forlani S, Iwabuchi K, Meiner V, Uyanik G, Erichsen AK, Feki I, Pasquier F, Belarbi S, Cruz VT, Depienne C, Truchetto J, Garrigues G, Tallaksen C, Tranchant C, Nishizawa M, Vale J, Coutinho P, Santorelli FM, Mhiri C, Brice A, Durr A; SPATAX consortium. Stevanin G, et al. Among authors: tada m. Brain. 2008 Mar;131(Pt 3):772-84. doi: 10.1093/brain/awm293. Epub 2007 Dec 13. Brain. 2008. PMID: 18079167

2

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

3

[Hereditary diffuse leukoencephalopathy with spheroids (HDLS): a review of the literature on its clinical characteristics and mutations in the colony-stimulating factor-1 receptor gene].

Konno T, Tada M, Tada M, Nishizawa M, Ikeuchi T. Konno T, et al. Among authors: tada m. Brain Nerve. 2014 May;66(5):581-90. Brain Nerve. 2014. PMID: 24807373 Review. Japanese.

4

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.

5

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. Neurology. 2014 Jan 14;82(2):139-48. doi: 10.1212/WNL.0000000000000046. Epub 2013 Dec 13. Neurology. 2014. PMID: 24336230 Free PMC article.

6

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

7

[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.

8

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.

9

[Oral cyclophosphamide therapy for multifocal fibrosclerosis with hypertrophic intracranial pachymeningitis].

Tada M, Onodera O, Hara K, Tanaka K, Takahashi H, Tsuji S, Nishizawa M. Tada M, et al. Rinsho Shinkeigaku. 2006 Feb;46(2):128-33. Rinsho Shinkeigaku. 2006. PMID: 16619837 Japanese.

10

Progressive myoclonus epilepsy: extraneuronal brown pigment deposition and system neurodegeneration in the brains of Japanese patients with novel SCARB2 mutations.

Fu YJ, Aida I, Tada M, Tada M, Toyoshima Y, Takeda S, Nakajima T, Naito H, Nishizawa M, Onodera O, Kakita A, Takahashi H. Fu YJ, et al. Among authors: tada m. Neuropathol Appl Neurobiol. 2014 Aug;40(5):551-63. doi: 10.1111/nan.12057. Neuropathol Appl Neurobiol. 2014. PMID: 23659519

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