Books, Original Papers & Review Papers- AOKI Masashi -
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[B]:Books [O]:Original Papers [R]:Review Papers
total:526
[2001]
401.[R] ALS models by transgenic animals.[Brain and Nerve,53, (2001), 799-807]M. Aoki, M. Nagai, M. Kato, Y. Itoyama
http://www.ncbi.nlm.nih.gov/pubmed/11596474 http://www.scopus.com/inward/record.url?eid=0034806120&partnerID=40
402.[R] [ALS models by transgenic animals] (No To Shinkei).[No To Shinkei,53(9), (2001), 799-807]Aoki M, Nagai M, Kato M, Itoyama Y
403.[R] 【遺伝子改変動物から神経変性疾患へのアプローチ】 トランスジェニック動物によるALSモデル.[脳と神経,53(9), (2001), 799-807]青木 正志, 永井 真貴子, 加藤 昌昭, 糸山 泰人
404.[O] Establishment of a local cooling model against spinal cord ischemia representing prolonged induction of heat shock protein..[J Thorac Cardiovasc Surg,122(2),(2001),351-357]Motoyoshi N, Sakurai M, Hayashi T, Aoki M, Abe K, Itoyama Y, Tabayashi K
405.[O] The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle..[Hum Mol Genet,10(17),(2001),1761-1766]Matsuda C, Hayashi Y K, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown R H Jr
406.[O] [An autopsy case of atypical Friedreich's ataxia with chronic idiopathic intestinal pseudo-obstruction].[Rinsho Shinkeigaku,41(7),(2001),412-417]Nagata T, Aoki M, Hasegawa T, Shiga Y, Hayashi T, Higuchi J, Abe K, Tanno T, Konno H, Itoyama Y
407.[O] Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy..[Neurology,57(2),(2001),271-278]Aoki M, Liu J, Richard I, Bashir R, Britton S, Keers S M, Oeltjen J, Brown H E, Marchand S, Bourg N, Beley C, McKenna-Yasek D, Arahata K, Bohlega S, Cupler E, Illa I, Majneh I, Barohn R J, Urtizberea J A, Fardeau M, Amato A, Angelini C, Bushby K, Beckmann J S, Brown R H Jr
408.[O] Familial amyotrophic lateral sclerosis with posterior column degeneration and basophilic inclusion bodies: a clinical, genetic and pathological study..[Clin Neuropathol,20(2),(2001),53-59]Tsuchiya K, Matsunaga T, Aoki M, Haga C, Ooe K, Abe K, Ikeda K, Nakano I
409.[O] [A family of early childhood-onset Charcot-Marie-Tooth disease type 2].[Rinsho Shinkeigaku,41(1),(2001),64-67]Hinuma Y, Aoki M, Takahashi T, Tateyama M, Nagai M, Yoshioka M, Itoyama Y
410.[O] 小児期早期より発症したCharcot-Marie-Tooth病2型の親子例.[臨床神経学,41(1),(2001),64-67]日沼 雄二, 青木 正志, 高橋 俊明, 竪山 真規, 永井 真貴子, 吉岡 勝, 糸山 泰人
411.[O] Amyotrophic lateral sclerosis-linked glutamate transporter mutant has impaired glutamate clearance capacity..[J Biol Chem,276(1),(2001),576-582]Trotti D, Aoki M, Pasinelli P, Berger U V, Danbolt N C, Brown R H Jr, Hediger M A
412.[R] LGMD2B(dysferlin deficiency).[Ryōikibetsu shōkōgun shirīzu, (2001), 84-87]M. Aoki
http://www.ncbi.nlm.nih.gov/pubmed/11555998 http://www.scopus.com/inward/record.url?eid=0035237626&partnerID=40
[2000]
413.[O] A family with oculopharyngeal muscular dystrophy with (GCG)9 expansion in which a sister had neck as well as proximal and her brother proximal lower limb muscle weakness.[Clinical Neurology,40,(2000),911-914]T. Takahashi, M. Tateyama, M. Aoki, Y. Shiga, E. Uyama, Y. Itoyama
http://www.ncbi.nlm.nih.gov/pubmed/11257788 http://www.scopus.com/inward/record.url?eid=0034461473&partnerID=40
414.[O] [A family with oculopharyngeal muscular dystrophy with (GCG)9 expansion in which a sister had neck as well as proximal and her brother proximal lower limb muscle weakness].[Rinsho Shinkeigaku,40(9),(2000),911-914]Takahashi T, Tateyama M, Aoki M, Shiga Y, Uyama E, Itoyama Y
415.[O] High prevalence of spinocerebellar ataxia type 1 (SCA1) in an isolated region of Japan..[J Neurol Sci,178(2),(2000),153-158]Onodera Y, Aoki M, Tsuda T, Kato H, Nagata T, Kameya T, Abe K, Itoyama Y
416.[O] Familial spinal arachnoiditis with secondary syringomyelia: clinical studies and MRI findings..[J Neurol Sci,177(1),(2000),60-64]Nagai M, Sakuma R, Aoki M, Abe K, Itoyama Y
417.[R] 【グルタミン酸 毒性からトランスポーターまで】 グルタミン酸トランスポーターとALS.[Brain Medical,12(2), (2000), 194-198]青木 正志
418.[R] 遠位型筋ジストロフィー(三好型)におけるdysferlin遺伝子異常 (特集 ミオパチー研究最前線).[神経研究の進歩,44(2), (2000), 204-211]青木 正志
419.[R] 【ミオパチー研究最前線】 遠位型筋ジストロフィー(三好型)におけるdysferlin遺伝子異常.[神経研究の進歩,44(2), (2000), 204-211]青木 正志
420.[R] 【三好型ミオパチー 臨床から遺伝子まで】 三好型遠位型筋ジストロフィーの原因遺伝子dysferlinの同定.[神経内科,52(3), (2000), 289-296]青木 正志
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