Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("KITAMOTO, Tetsuyuki")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 13 of 13

  • Page / 1
Export

Selection :

  • and

Novel α-secretase cleavage of Alzheimer's amyloid β precursor protein in the endoplasmic reticulum of COS7 cellsSHIN, Ryong-Woon; SAIDO, Takaomi C; MAEDA, Masahiro et al.Neuroscience letters. 2005, Vol 376, Num 1, pp 14-19, issn 0304-3940, 6 p.Article

A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesisIWASAKI, Yasushi; KIZAWA, Mayuki; HORI, Norio et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2009, Vol 111, Num 7, pp 606-609, issn 0303-8467, 4 p.Article

A novel trivalent cation chelator Feralex dissociates binding of aluminum and iron associated with hyperphosphorylated τ of Alzheimer's diseaseSHIN, Ryong-Woon; KRUCK, Theo P. A; MURAYAMA, Harunobu et al.Brain research. 2003, Vol 961, Num 1, pp 139-146, issn 0006-8993, 8 p.Article

A unique case of sporadic Creutzfeldt-Jacob disease presenting as progressive supranuclear palsySHIMAMURA, Munehisa; UYAMA, Eiichiro; HIRANO, Teruyuki et al.Internal medicine (Tokyo. 1992). 2003, Vol 42, Num 2, pp 195-198, issn 0918-2918, 4 p.Article

Co-Occurrence of Types 1 and 2 PrPres in Sporadic Creutzfeldt-Jakob Disease MM1KOBAYASHI, Atsushi; MIZUKOSHI, Kenta; IWASAKI, Yasushi et al.The American journal of pathology. 2011, Vol 178, Num 3, pp 1309-1315, issn 0002-9440, 7 p.Article

Experimental Verification of a Traceback Phenomenon in Prion InfectionKOBAYASHI, Atsushi; SAKUMA, Nobuyuki; MATSUURA, Yuichi et al.Journal of virology. 2010, Vol 84, Num 7, pp 3230-3238, issn 0022-538X, 9 p.Article

Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP)NISHIMOTO, Yoshinori; ITO, Daisuke; SUZUKI, Shigeaki et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2011, Vol 113, Num 8, pp 696-698, issn 0303-8467, 3 p.Article

Familial Creutzfeldt-Jakob Disease with a V1801 Mutation: Comparative Analysis with Pathological Findings and Diffusion-Weighted ImagesMUTSUKURA, Kazuo; SATOH, Katsuya; EGUCHI, Katsumi et al.Dementia and geriatric cognitive disorders. 2009, Vol 28, Num 6, pp 550-557, issn 1420-8008, 8 p.Article

Advanced glycation end products (AGE) and their receptor (RAGE) in the brain of patients with Creutzfeldt-Jakob disease with prion plaquesSASAKI, Nobuyuki; TAKEUCHI, Masayoshi; MAKITA, Zenji et al.Neuroscience letters. 2002, Vol 326, Num 2, pp 117-120, issn 0304-3940Article

Iron (III) induces aggregation of hyperphosphorylated τ and its reduction to iron (II) reverses the aggregation: implications in the formation of neurofibrillary tangles of Alzheimer's diseaseYAMAMOTO, Akira; SHIN, Ryong-Woon; HASEGAWA, Kazuhiro et al.Journal of neurochemistry. 2002, Vol 82, Num 5, pp 1137-1147, issn 0022-3042, 11 p.Article

Creutzfeldt-Jakob disease with the M232R mutation in the prion protein gene in two cases showing different disease courses: A clinicopathological studyTAKEDA, Naoya; YOKOTA, Osamu; ISHIZU, Hideki et al.Journal of the neurological sciences. 2012, Vol 312, Num 1-2, pp 108-116, issn 0022-510X, 9 p.Article

Prospective 10-year surveillance of human prion diseases in JapanNOZAKI, Ichiro; HAMAGUCHI, Tsuyoshi; SHIGA, Yusei et al.Brain. 2010, Vol 133, pp 3043-3057, issn 0006-8950, 15 p., 10Article

Unique clinicopathological features and PrP profiles in the first autopsied case of dura mater graft-associated Creutzfeldt―Jakob disease with codon 219 lysine allele observed in Japanese populationIKAWA, Masamichi; YONEDA, Makoto; MATSUNAGA, Akiko et al.Journal of the neurological sciences. 2009, Vol 285, Num 1-2, pp 265-267, issn 0022-510X, 3 p.Article

  • Page / 1