T Makifuchi
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Explore the profile of T Makifuchi including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
276
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Recent Articles
1.
Yanase D, Komai K, Hamaguchi T, Okino S, Yokoji H, Makifuchi T, et al.
Neurology
. 2004 Dec;
63(11):2149-52.
PMID: 15596767
The authors report an unusual family with hereditary spastic paraplegia (HSP) with frontal lobe dysfunction having the onset in the sixth decade. All the patients showed hypoperfusion in the frontal...
2.
Ishida C, Kakishima A, Okino S, Furukawa Y, Kano M, Oda Y, et al.
Neurology
. 2003 Feb;
60(3):514-7.
PMID: 12578942
The authors report a 75-year-old woman with atypical sporadic Creutzfeldt-Jakob disease (CJD) characterized by MM1-type prion protein (PrP) (methionine homozygosity at codon 129 in the PrP gene and type-1 protease-resistant...
3.
Koide T, Ohtake H, Nakajima T, Furukawa H, Sakai K, Kamei H, et al.
Neurology
. 2002 Nov;
59(10):1619-21.
PMID: 12451207
The authors describe a patient who had a point mutation at codon 232 of the prion protein gene, resulting in the substitution of methionine for arginine (M232R). The patient developed...
4.
Chui D, Dobo E, Makifuchi T, Akiyama H, Kawakatsu S, Petit A, et al.
J Alzheimers Dis
. 2002 Sep;
3(2):231-239.
PMID: 12214064
It is widely accepted that Abeta plays a pivotal role in the pathogenesis of Alzheimer's disease (AD) [27]. Attention has been focused mainly on how extracellular Abeta exerts its effects...
5.
Yamazaki M, Makifuchi T, Chen K, Mori O, Katayama Y, Takahashi H, et al.
Acta Neuropathol
. 2001 Nov;
102(5):510-4.
PMID: 11699567
This is the first report demonstrating that progressive supranuclear palsy (PSP) exists on Guam. This 75-year-old Guamanian Chamorro patient with slight dementia and rigidity with restriction of ocular up gaze...
6.
Ishikawa K, Owada K, Ishida K, Fujigasaki H, Shun Li M, Tsunemi T, et al.
Neurology
. 2001 Jun;
56(12):1753-6.
PMID: 11425948
Aggregations of the alpha1A-calcium channel protein have been previously demonstrated in spinocerebellar ataxia type 6 (SCA6). Here the authors show that small aggregates, labeled by a monoclonal antibody 1C2 that...
7.
Imai C, Sugai T, Iritani S, Niizato K, Nakamura R, Makifuchi T, et al.
Neurosci Lett
. 2001 Jun;
305(3):185-8.
PMID: 11403936
The application of DNA array technology to schizophrenic studies enabled us to assess molecular features of this disease. The expression of synapsin II and N-ethylmaleimide-sensitive fusion protein (NSF) mRNAs is...
8.
Nakayama H, Kiatipattanasakul W, Nakamura S, Miyawaki K, Kikuta F, Uchida K, et al.
Neurosci Lett
. 2001 Jan;
297(3):195-8.
PMID: 11137761
In the present study, the fractal dimension (FD), a concept to determine morphological complexity, was applied to morphological estimation of animal and human senile plaque using a computer-aided method. The...
9.
Sato N, Imaizumi K, Manabe T, Taniguchi M, Hitomi J, Katayama T, et al.
J Biol Chem
. 2000 Oct;
276(3):2108-14.
PMID: 11031265
An alternative spliced form of the presinilin 2 (PS2) gene (PS2V) lacking exon 5 has previously been reported to be expressed in human brains in sporadic Alzheimer's disease (AD). PS2V...
10.
Fujigasaki H, Uchihara T, Koyano S, Iwabuchi K, Yagishita S, Makifuchi T, et al.
Exp Neurol
. 2000 Sep;
165(2):248-56.
PMID: 10993685
Machado-Joseph disease (MJD)/spinocerebellar ataxia type 3 (SCA3) is one of the dominantly inherited cerebellar ataxias. The gene responsible for the disease, a novel gene of unknown function, encodes ataxin-3 containing...