Books, Original Papers & Review Papers- AOKI Masashi -
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[B]:Books [O]:Original Papers [R]:Review Papers
total:479
[1999]
381.[R] LGMD(肢帯型筋ジストロフィー)の概観 ポジショナルクローニングによる三好型遠位型筋ジストロフィーの原因遺伝子dysferlinの同定.[臨床神経学,39(12), (1999), 1272-1275]青木 正志, 荒畑 喜一, Brown Robert H.Jr.
382.[R] Positional cloning of the gene for Miyoshi myopathy and limb-girdle muscular dystrophy.[Clinical Neurology,39, (1999), 1272-1275]Masashi Aoki, Kiichi Arahata, Robert H. Brown
http://www.ncbi.nlm.nih.gov/pubmed/10791095 http://www.scopus.com/inward/record.url?eid=0033495164&partnerID=40
383.[R] ALSとグルタミン酸トランスポーター (運動ニューロン疾患).[医学のあゆみ,191(8), (1999), 817-820]青木 正志
384.[R] 【ミオパチー update】 進行性筋ジストロフィーとその類縁疾患 三好型遠位型筋ジストロフィー ポジショナルクローニングによる原因遺伝子dysferlinの同定.[Clinical Neuroscience,17(10), (1999), 1146-1148]青木 正志
385.[O] Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy..[Neurology,53(5),(1999),1119-1122]Matsuda C, Aoki M, Hayashi Y K, Ho M F, Arahata K, Brown R H Jr
386.[O] Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect..[J Med Genet,36(2),(1999),112-114]Mizushima K, Watanabe M, Kondo I, Okamoto K, Shizuka M, Abe K, Aoki M, Shoji M
[1998]
387.[O] Stress protein inductions after brain ischemia..[Cell Mol Neurobiol,18(6),(1998),709-719]Abe K, Kawagoe J, Aoki M, Kogure K, Itoyama Y
388.[O] Molecular analyses of the Cu/Zn superoxide dismutase gene in patients with familial amyotrophic lateral sclerosis (ALS) in Japan. (Cell Mol Neurobiol).[Cell Mol Neurobiol,18(6),(1998),639-647]Aoki M, Abe K, Itoyama Y
389.[R] Molecular analyses of the Cu/Zn superoxide dismutase gene in patients with familial amyotrophic lateral sclerosis (ALS) in Japan. (Cell Mol Neurobiol).[Cell Mol Neurobiol,18(6), (1998), 639-647]Aoki M, Abe K, Itoyama Y
390.[O] Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy..[Nat Genet,20(1),(1998),31-36]Liu J, Aoki M, Illa I, Wu C, Fardeau M, Angelini C, Serrano C, Urtizberea J A, Hentati F, Hamida M B, Bohlega S, Culper E J, Amato A A, Bossie K, Oeltjen J, Bejaoui K, McKenna-Yasek D, Hosler B A, Schurr E, Arahata K, de Jong P J, Brown R H Jr
391.[O] Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis..[Ann Neurol,43(5),(1998),645-653]Aoki M, Lin C L, Rothstein J D, Geller B A, Hosler B A, Munsat T L, Horvitz H R, Brown R H Jr
392.[O] Enhancement of heat shock protein expression after transient ischemia in the preconditioned spinal cord of rabbits..[J Vasc Surg,27(4),(1998),720-725]Sakurai M, Hayashi T, Abe K, Aoki M, Sadahiro M, Tabayashi K
393.[O] Mitochondrial DNA deletion is a predisposing cause for sensorineural hearing loss..[Laryngoscope,108(4 Pt 1),(1998),580-584]Ueda N, Oshima T, Ikeda K, Abe K, Aoki M, Takasaka T
394.[O] Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics..[J Neurol Sci,156(2),(1998),180-185]Mizushima K, Watanabe M, Abe K, Aoki M, Itoyama Y, Shizuka M, Okamoto K, Shoji M
395.[O] Blood distribution in the facial nerve in temporal bones acquired from cases with subarachnoid hemorrhage.[Laryngoscope,108,(1998),580-584]Narihisa Ueda, Takeshi Oshima, Katsuhisa Ikeda, Koji Abe, Masashi Aoki, Tomonori Takasaka
10.1097/00005537-199804000-00022
http://www.scopus.com/inward/record.url?eid=70350411987&partnerID=40
396.[O] Enhancement of heat shock protein expression after transient ischemia in the preconditioned spinal cord of rabbits.[Journal of Vascular Surgery,27,(1998),720-725]M. Sakurai, T. Hayashi, K. Abe, M. Aoki, M. Sadahiro, K. Tabayashi
10.1016/S0741-5214(98)70238-1
http://www.ncbi.nlm.nih.gov/pubmed/9576086 http://www.scopus.com/inward/record.url?eid=0031939159&partnerID=40
[1997]
397.[O] Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis..[J Neurol Sci,150(2),(1997),133-135]Shizuka M, Watanabe M, Aoki M, Ikeda Y, Mizushima K, Okamoto K, Itoyama Y, Abe K, Shoji M
398.[O] A presenilin-1 mutation in a Japanese family with Alzheimer's disease and distinctive abnormalities on cranial MRI..[Neurology,48(4),(1997),1118-1120]Aoki M, Abe K, Oda N, Ikeda M, Tsuda T, Kanai M, Shoji M, St George-Hyslop P H, Itoyama Y
399.[O] A novel missense point mutation (S134N) of the Cu/Zn superoxide dismutase gene in a patient with familial motor neuron disease..[Hum Mutat,9(1),(1997),69-71]Watanabe M, Aoki M, Abe K, Shoji M, Iizuka T, Ikeda Y, Hirai S, Kurokawa K, Kato T, Sasaki H, Itoyama Y
400.[O] Ocular changes in patients with spinocerebellar degeneration and repeated trinucleotide expansion of spinocerebellar ataxia type 1 gene..[Arch Ophthalmol,115(2),(1997),231-236]Abe T, Abe K, Aoki M, Itoyama Y, Tamai M
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