Altered trafficking and adhesion function of MPZ mutations and phenotypes of Charcot-Marie-Tooth disease 1BMATSUYAMA, Wataru; NAKAGAWA, Masanori; TAKASHIMA, Hiroshi et al.Acta neuropathologica. 2002, Vol 103, Num 5, pp 501-508, issn 0001-6322Article

Non-destructive detection of defects in carbon fiber-reinforced carbon matrix composites using SQUID : Superconducting electronic devices and their applicationsKASAI, Naoko; HATSUKADE, Yoshimi; TAKASHIMA, Hiroshi et al.IEICE transactions on electronics. 2005, Vol 88, Num 2, pp 180-187, issn 0916-8524, 8 p.Article

Electroluminescence near interfaces between (Ca,Sr)TiO₃:Pr phosphor and SnO₂:Sb transparent conductor thin films prepared by sol-gel and spin-coating methodsKYOMEN, Tôru; HANAYA, Minoru; TAKASHIMA, Hiroshi et al.Journal of luminescence. 2014, Vol 149, pp 133-137, issn 0022-2313, 5 p.Article

Adsorption of Anionic Nanosheets from Their Dilute Colloidal Suspensions onto Gas—Liquid Interfaces with and without a Langmuir Film of Cationic SurfactantIKEGAMI, Keiichi; TETSUKA, Hiroyuki; HOSHI, Yasushi et al.Langmuir. 2010, Vol 26, Num 4, pp 2514-2520, issn 0743-7463, 7 p.Article

Influence of a degraded SrTiO₃ layer at the YBa₂Cu₃O_7-δ-SrTiO₃ interface on the dielectric behavior at cryogenic temperatureTAKASHIMA, Hiroshi; RUIPING WANG; OKANO, Makoto et al.Cryogenics (Guildford). 2005, Vol 45, Num 4, pp 300-303, issn 0011-2275, 4 p.Article

Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathyBOLINO, Alessandra; LONIE, Lorne J; ZIMMER, Michael et al.Neurogenetics (Oxford. Print). 2001, Vol 3, Num 2, pp 107-109, issn 1364-6745Article

Human T-Lymphotropic Virus Type I (HTLV-I)-Specific CD8+ Cells Accumulate in the Lungs of Patients Infected With HTLV-I With Pulmonary InvolvementKAWABATA, Takashi; HIGASHIMOTO, Ikkou; TAKASHIMA, Hiroshi et al.Journal of medical virology. 2012, Vol 84, Num 7, pp 1120-1127, issn 0146-6615, 8 p.Article

Investigation of temperature dependence of microwave-induced characteristics of a NbN Josephson junction arraySHOJI, Akira; TAKASHIMA, Hiroshi; MURUGESAN, Mariappan et al.IEEE transactions on applied superconductivity. 2005, Vol 15, Num 2, pp 205-208, issn 1051-8223, 4 p., 1Conference Paper

Capacitance temperature sensor using epitaxial SrTiO₃ film with a single-crystal-like behaviorTAKASHIMA, Hiroshi; RUIPING WANG; SHIRAKAWA, Naoki et al.Thin solid films. 2005, Vol 486, Num 1-2, pp 145-148, issn 0040-6090, 4 p.Conference Paper

Validity of sentinel lymph node concept for patients with prostate cancerTAKASHIMA, Hiroshi; EGAWA, Masayuki; IMAO, Tetsuya et al.The Journal of urology. 2004, Vol 171, Num 6, pp 2268-2271, issn 0022-5347, 4 p., 1Article

CMT4A: Identification of a Hispanic GDAP1 founder mutationBOERKOEL, Cornelius F; TAKASHIMA, Hiroshi; NAKAGAWA, Masanori et al.Annals of neurology. 2003, Vol 53, Num 3, pp 400-405, issn 0364-5134, 6 p.Article

Charcot-Marie-Tooth disease and related neuropathies: Mutation distribution and genotype-phenotype correlationBOERKOEL, Cornelius F; TAKASHIMA, Hiroshi; WILLIAMS, Lowell L et al.Annals of neurology. 2002, Vol 51, Num 2, pp 190-201, issn 0364-5134Article

Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathyTAKASHIMA, Hiroshi; BOERKOEL, Cornelius F; STOCKTON, David W et al.Nature genetics. 2002, Vol 32, Num 2, pp 267-272, issn 1061-4036, 6 p.Article

Periaxin mutations cause recessive Dejerine-Sottas neuropathyBOERKOEL, Cornelius F; TAKASHIMA, Hiroshi; STANKIEWICZ, Pawel et al.American journal of human genetics. 2001, Vol 68, Num 2, pp 325-333, issn 0002-9297Article

Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutationJUNHUI YUAN; MATSUURA, Eiji; HIGUCHI, Yujiro et al.Neurology. 2013, Vol 80, Num 18, pp 1641-1649, issn 0028-3878, 9 p.Article

Vincristine exacerbates asymptomatic Charcot-Marie-Tooth disease with a novel EGR2 mutationNAKAMURA, Tomonori; HASHIGUCHI, Akihiro; SUZUKI, Shinsuke et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 1, pp 77-82, issn 1364-6745, 6 p.Article

Significance of dysadherin and E-cadherin expression in differentiated-type gastric carcinoma with submucosal invasionMAEHATA, Yoshitomo; HIRAHASHI, Minako; AISHIMA, Shinichi et al.Human pathology. 2011, Vol 42, Num 4, pp 558-567, issn 0046-8177, 10 p.Article

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N geneOKAMOTO, Yuji; TAKASHIMA, Hiroshi; IZUMO, Shuji et al.Neurogenetics (Oxford. Print). 2006, Vol 7, Num 3, pp 175-183, issn 1364-6745, 9 p.Article

Fe content dependence of synthetic-antiferromagnetic coupling in subnano-crystalline FeCoB/Ru/FeCoB filmsHASHIMOTO, Atsushi; SAITO, Shin; DONG YOUNG KIM et al.IEEE transactions on magnetics. 2006, Vol 42, Num 10, pp 2342-2344, issn 0018-9464, 3 p.Conference Paper

Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequenceNAKAGAWA, Masanori; TAKASHIMA, Hiroshi; UMEHARA, Fujio et al.Journal of the neurological sciences. 2001, Vol 185, Num 1, pp 31-37, issn 0022-510XArticle

Characterization of the immunophenotype of the tumor budding and its prognostic implications in squamous cell carcinoma of the lungTAIRA, Tetsuhiko; ISHII, Genichiro; TAKASHIMA, Hiroshi et al.Lung cancer. 2012, Vol 76, Num 3, pp 423-430, issn 0169-5002, 8 p.Article

A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutationKINOSHITA, Takashi; IMAIZUMI, Toshihiro; MIURA, Yumiko et al.Neuroscience letters. 2003, Vol 350, Num 3, pp 169-172, issn 0304-3940, 4 p.Article

Detection of the 14-3-3 protein in the cerebrospinal fluid of Japanese multiple sclerosis patients presenting with severe myelitisSATOH, Jun-Ichi; YUKITAKE, Motohiro; KUROHARA, Kazuhiro et al.Journal of the neurological sciences. 2003, Vol 212, Num 1-2, pp 11-20, issn 0022-510X, 10 p.Article

EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathyBOERKOEL, Cornelius F; TAKASHIMA, Hiroshi; BACINO, Carlos A et al.Neurogenetics (Oxford. Print). 2001, Vol 3, Num 3, pp 153-157, issn 1364-6745Article

Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin geneNAKAGAWA, Masanori; MATSUZAKI, Toshio; SUEHARA, Masahito et al.Journal of the neurological sciences. 2001, Vol 184, Num 1, pp 15-19, issn 0022-510XArticle