論文 Triggering factors for febrile attacks in Japanese patients with familial Mediterranean fever Clin Exp Rheumatol,127(5):76-79 2020 Author:Kishida D, Nakamura A, Yazaki M, Oka K, Tsuchiya-Suzuki A, Ichikawa T, Shimojima Y, Sekijima Y.
Late-onset familial Mediterranean fever in Japan Mod Rheumatol,25:1-4 2020 Author:Kishida D, Yazaki M, Nakamura A, Tsuchiya-Suzuki A, Shimojima Y, Sekijima Y
iPS細胞を用いたDMDに対するエクソン・スキップ治療の開発 別冊 BIO Clinica,9(2):129-134 2020 Author:中村昭則、他
Examining the Validity of Efforts of the Muscular Dystrophy Medical Network in Nagano : A Questionnaire Study 信州医学雑誌,66(3):205-210 2018(Jun. 10) Author:Nishizawa, Hitomi; Takahashi, Hiroko; Aoki, Kaoru; Kosho, Tomoki; Inaba, Yuji; Nakamura, Akinori
Periodic sound-based 6-minute walk test for patients with Duchenne muscular dystrophy: a preliminary study JOURNAL OF PHYSICAL THERAPY SCIENCE,27(11):3473-3479 2015(Nov.) Author:Nishizawa, Hitomi; Genno, Hirokazu; Shiba, Naoko; Nakamura, Akinori;
Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE,1852(10):2170-2182 2015(Oct.) Author:Shiba, Naoko; Miyazaki, Daigo; Yoshizawa, Takahiro; Fukushima, Kazuhiro; Shiba, Yuji; Inaba, Yuji; Imamura, Michihiro; Takeda, Shin'ichi; Koike, Kenichi; Nakamura, Akinori;
Long-Term Efficacy of Systemic Multiexon Skipping Targeting Dystrophin Exons 45-55 With a Cocktail of Vivo-Morpholinos in Mdx52 Mice MOLECULAR THERAPY-NUCLEIC ACIDS,4 2015(Feb.) Author:Echigoya, Yusuke; Aoki, Yoshitsugu; Miskew, Bailey; Panesar, Dharminder; Touznik, Aleksander; Nagata, Tetsuya; Tanihata, Jun; Nakamura, Akinori; Nagaraju, Kanneboyina; Yokota, Toshifumi;
Periodic sound-based 6-minute walk test for patients with Duchenne muscular dystrophy: a preliminary study J. Phys. Ther. Sci.,27:3473-3479 2015 Author:Hitomi Nishizawa, Hirokazu Genno, Naoko Shiba, Akinori Nakamura
Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer. Cerebellum Ataxias 2015 Author:Matsushima A, Yoshida K, Genno H, Murata A, Matsuzawa S, Nakamura K, Nakamura A, Ikeda S.
Identification of Disease-Promoting HLA Class I and Protective Class II Modifiers in Japanese Patients with Familial Mediterranean Fever PLOS ONE,10(5) 2015 Author:Yasunami, Michio; Nakamura, Hitomi; Agematsu, Kazunaga; Nakamura, Akinori; Yazaki, Masahide; Kishida, Dai; Yachie, Akihiro; Toma, Tomoko; Masumoto, Junya; Ida, Hiroaki; Koga, Tomohiro; Kawakami, Atsushi; Eguchi, Katsumi; Furukawa, Hiroshi; Nakamura, Tadashi; Nakamura, Minoru; Migita, Kiyoshi;
One year changes in PiB SUVR values in Alzheimer's disease, amnestic cognitive impairment, and cognitively normal subjects JOURNAL OF NUCLEAR MEDICINE,56(3) 2015 Author:Kato, Takashi; Iwata, Kaori; Fujiwara, Ken; Inui, Yoshitaka; Fukaya, Naohiko; Ito, Kengo; Nakamura, Akinori;
Slowly progressing lower motor neuron disease caused by a novel duplication mutation in exon 1 of the SOD1 gene NEUROBIOLOGY OF AGING,35(10) 2014(Oct.) Author:Nakamura, Akinori; Kuru, Satoshi; Hineno, Akiyo; Kobayashi, Chinatsu; Kinoshita, Tomomi; Miyazaki, Daigo; Ikeda, Shu-ichi;
Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations ARTHRITIS RESEARCH & THERAPY,16(5) 2014 Author:Kishida, Dai; Nakamura, Akinori; Yazaki, Masahide; Tsuchiya-Suzuki, Ayako; Matsuda, Masayuki; Ikeda, Shu-ichi;
Genotype-phenotype correlations in Japanese patients with familial Mediterranean fever. Medicine,93:158-164 2014 Author:Nonaka F, Agematsu K, Yazaki M, Yachie A, Nakamura A, Toma T, Kishida D, Uehara R, Nakamura Y, Jiuchi Y, Masumoto J, Furukawa H, Ida H, Terai C, Kawakami A, Katsumi Eguchi, Michio Yasunami, Migita K.
在宅難病患者家族への総合在宅遠隔医療システムの開発 日本遠隔医療学会雑誌,9(2):74-78 2013(Oct.) Author:滝沢 正臣; 中村 昭則; 武井 洋一; Keywords:telemedicine; tablet; electronic medical care record; tele-vital-monitoring;
タブレット端末を用いた診療情報共有の有効性評価 (JTTA 2013 TAKAMATSU 第17回日本遠隔医療学会学術大会 : 遠隔医療による国際協力と日本版EHRの確立を目指して) -- (在宅医療支援と評価) 日本遠隔医療学会雑誌,9(2):148-151 2013(Oct.) Author:宮崎 大吾; 中村 昭則; 日根野 晃代; Keywords:難病; 重症心身障害; 在宅診療; 診療情報共有; タブレット端末; intractable disease; severe motor and intellectual disabilities; home care; health information exchange; tablet-type device;
alpha-Synuclein coaggregation in familial amyotrophic lateral sclerosis with SOD1 gene mutation HUMAN PATHOLOGY,44(6):1171-1176 2013(Jun.) Author:Takei, Yo-ichi; Oguchi, Kenya; Koshihara, Hiroshi; Hineno, Akiyo; Nakamura, Akinori; Ohara, Shinji;
Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-alpha 2 chain-null congenital muscular dystrophy mice HUMAN MOLECULAR GENETICS,22(24):4914-4928 2013 Author:Aoki, Yoshitsugu; Nagata, Tetsuya; Yokota, Toshifumi; Nakamura, Akinori; Wood, Matthew J. A.; Partridge, Terence; Takeda, Shin'ichi;
信州大学医学部附属病院難病診療センターによる長野県神経難病患者の在宅療養支援の現状と課題 信州医学雑誌 = The Shinshu medical journal,61(6):397-403 2013 Author:中村 昭則; 吉田 邦広; 松沢 由美; 両角 由里; 池田 修一; Keywords:intractable disease; support of home-care; house-call medical care; respite care; 難病; 在宅療養支援; 訪問診療; 短期一時入院;
Molecular Mechanism and Development of Antisense Therapy for Duchenne Muscular Dystrophy J Nerological Dis & Strokes,1(3):1021 2013 Author:Nakamura A
Availability of RT-PCR analysis on the early diagnosis for dystrophinopathy having a nonsense mutation J Neurol & Translation Neurosc,1:1005 2013 Author:Narumi Y, Fueki N, Kosho T, Hayashi Y, Nishino I, Nakamura A
Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin alpha2 chain-null congenital muscular dystrophy mice Hum Mol Genet,22:4914-4928 2013 Author:Aoki Y, Nagata T, Yokota T, Nakamura A, Wood MJ, Partridge T, Takeda S
Initial Pulmonary Respiration Causes Massive Diaphragm Damage and Hyper-CKemia in Duchenne Muscular Dystrophy Dog Scientific Reports,3:2183 2013 Author:Nakamura A, Kobayashi M, Kuraoka M, Yuasa K, Yugeta N, Okada T, Takeda S
a-synuclein co-aggregation in amyotrophic laterak sclerosis with SOD1 C111Y mutation Hum Pathol,44:1171-1176 2013 Author:Takei Y, Oguchi K, Koshihara H, Hineno A, Nakamura A, Ohara S
Extensive and prolonged restoration of dystrophin expression with vivo-morpholino-mediated multiple exon skipping in dystrophic dogs Nucl Acid Ther,22:306-315 2012 Author:Yokota T, Nakamura A, Saito T, Nagata T, Partridge T, Hoffman E, Takeda S
Bodywide skipping of exon 45-55 in dystrophic mdx52 mice by systemic antisense delivery PNAS,109:13763-13768 2012 Author:Aoki Y, Yokota T, Nagata T, Nakamura A, Tanihita J, Saito T, Duguez S, Nagaraju K, Hoffman E, Partridge T, Takeda S
Familial Mediterranean Fever in Japan Medicine,91:337-343 2012 Author:Migita K, Uehara R, Nakamura Y, Yasunami M, Tsuchiya-Suzuki A, Yazaki M, Nakamura A, Masumoto J, Yachie A, Furukawa H, Ishibashi H, Ida H, Yamazaki K, Kawakami A, Agematsu K.
Distinctive clinicopathological features in two large families with amyotrophic lateral sclerosis associated having a L106V mutation in the SOD1 gene J Neurol Sci,319:63-74 2012 Author:Hineno A, Nakamura A, Yoshida K, Shimojima Y, Oyanagai K, Ikeda S
Marked intrafaimilial phenotypic variation in a family with SOD1 C111Y mutation Amyotrophic Lateral Sclerosis,13(5):479-486 2012 Author:Nakamura A, Hineno A, Yoshida K,Takei Y, Hanaoka-Tachibana N, Sekijima Y, Ohara S, Ikeda S
Long-term engraftment of multipotent mesenchymal stromal cells that can differentiate to form myogenic cells in dogs with Duchenne muscular dystrophy Mol Ther,20:168-177 2012 Author:Nitahara-Kasahara Y, Hayashita-Kinoh H, Shin JH, Ohshima-Hosoyama S, Nishiyama A, Kobayashi M, Okada H, Wada-Maeda M, Nakamura A, Okada T, Takeda S
Identification of Muscle-Specific MicroRNAs in Serum of Muscular Dystrophy Animal Models: Promising Novel Blood-Based Markers for Muscular Dystrophy PLOS ONE,6(3) 2011 Author:Mizuno, Hideya; Nakamura, Akinori; Aoki, Yoshitsugu; Ito, Naoki; Kishi, Soichiro; Yamamoto, Kazuhiro; Sekiguchi, Masayuki; Takeda, Shin'ichi; Hashido, Kazuo;
Dystrophin-deficient muscular dystrophy in an Alaskan malamute Vet Rec,169:127-129 2011 Author:Ito D, Kitagawa M, Jeffery N, Okada M, Yoshida M, Kobayashi M, Nakamura A, Watari T.
Mammalian Models of Duchenne Muscular Dystrophy: Pathological Characteristics and Therapeutic Applications J Biomed Biotech,2011:187393 2011 Author:Nakamura A, Takeda S
CELL THERAPEUTIC APPROACH TO DUCHENNE MUSCULAR DYSTROPHY USING MYOGENIC DIFFERENTIATION OF MULTIPOTENT MESENCYMAL STROMAL CELLS IN DOG JOURNAL OF GENE MEDICINE,12(12):1063-1064 2010(Dec.) Author:Nitahara-Kasahara, Yuko; Hayashita-Kinoh, Hiromi; Shin, Jin-Hong; Nishiyama, Akiyo; Ohshima-Hosoyama, Sachiko; Wada-Maeda, Michiko; Nakamura, Akinori; Okada, Takashi; Takeda, Shin'ichi;
In-frame Dystrophin Following Exon 51-Skipping Improves Muscle Pathology and Function in the Exon 52-Deficient mdx Mouse MOLECULAR THERAPY,18(11):1995-2005 2010(Nov.) Author:Aoki, Yoshitsugu; Nakamura, Akinori; Yokota, Toshifumi; Saito, Takashi; Okazawa, Hitoshi; Nagata, Tetsuya; Takeda, Shin'ichi;
Antisense PMO Found in Dystrophic Dog Model Was Effective in Cells from Exon 7-Deleted DMD Patient PLOS ONE,5(8) 2010 Author:Saito, Takashi; Nakamura, Akinori; Aoki, Yoshitsugu; Yokota, Toshifumi; Okada, Takashi; Osawa, Makiko; Takeda, Shin'ichi;
EVALUATION OF DYSTROPHIC DOG PATHOLOGY BY FAT-SUPPRESSED T2-WEIGHTED IMAGING MUSCLE & NERVE,40(5):815-826 2009(Nov.) Author:Kobayashi, Masanori; Nakamura, Akinori; Hasegawa, Daisuke; Fujita, Michio; Orima, Hiromitsu; Takeda, Shin'ichi;
Clinical and Genetic Features of Familial Mediterranean Fever in Japan JOURNAL OF RHEUMATOLOGY,36(8):1671-1676 2009(Aug.) Author:Tsuchiya-Suzuki, Ayako; Yazaki, Masahide; Nakamura, Akinori; Yamazaki, Kazuko; Agematsu, Kazunaga; Matsuda, Masayuki; Ikeda, Shu-Ichi;
Efficacy of Systemic Morpholino Exon-Skipping in Duchenne Dystrophy Dogs ANNALS OF NEUROLOGY,65(6):667-676 2009(Jun.) Author:Yokota, Toshifumi; Lu, Qi-long; Partridge, Terence; Kobayashi, Masanori; Nakamura, Akinori; Takeda, Shin'ichi; Hoffman, Eric;
In Vitro Analysis of Antisense Phosphorodiamidate Morpholino Oligomer Mediated Multi-Exon Skipping in Dystrophic Dog Derived Cells MOLECULAR THERAPY,17:S387-S387 2009(May) Author:Saito, Takashi; Nakamura, Akinori; Aoki, Yoshitsugu; Yokota, Toshifumi; Osawa, Makiko; Takeda, Shin'ichi;
Exon 51 Skipping by Morpholinos Can Restore Dystrophin Expression, Muscle Pathology and Function in Exon 52-Deficient mdx52 Mice MOLECULAR THERAPY,17:S386-S386 2009(May) Author:Aoki, Yoshitsugu; Yokota, Toshifumi; Saito, Takashi; Nakamura, Akinori; Takeda, Shin'ichi;
Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene JOURNAL OF HUMAN GENETICS,54(2):127-130 2009(Feb.) Author:Miyazaki, Daigo; Yoshida, Kunihiro; Fukushima, Kazuhiro; Nakamura, Akinori; Suzuki, Kayo; Sato, Toshiyuki; Takeda, Shin'ichi; Ikeda, Shu-ichi;
A Renaissance for Antisense Oligonucleotide Drugs in Neurology Exon Skipping Breaks New Ground ARCHIVES OF NEUROLOGY,66(1):32-38 2009(Jan.) Author:Yokota, Toshifumi; Takeda, Shin'ichi; Lu, Qi-Long; Partridge, Terence A.; Nakamura, Akinori; Hoffman, Eric P.;
Noninvasive evaluation of pathological change in canine X-linked muscular dystrophy in Japan by fat-suppressed T2-weighted imaging Muscle Nerve,40:815-826 2009 Author:Kobayashi M, Nakamura A, Hasegawa D, Orima H, Takeda S
Clinical and genetic features of familial Mediterranean fever in Japan J Rheumatol,36:1671-1676 2009 Author:Tsuchiya-Suzuki A, Yazaki M, Nakamura A. Yamazaki K, Agematsu K, Matsuda M, Ikeda S
Exon skipping therapy in Duchenne muscular dystrophy Neuropathol,29:494-501 2009 Author:Nakamura A, Takeda S
MicroRNA-206 Is Highly Expressed in Newly Formed Muscle Fibers: Implications Regarding Potential for Muscle Regeneration and Maturation in Muscular Dystrophy CELL STRUCTURE AND FUNCTION,33(2):163-169 2008 Author:Yuasa, Katsutoshi; Hagiwara, Yasuko; Ando, Masanori; Nakamura, Akinori; Takeda, Shin'ichi; Hijikata, Takao;
Dystrophin deficiency in canine X-linked muscular dystrophy in Japan (CXMD(J)) alters myosin heavy chain expression profiles in the diaphragm more markedly than in the tibialis cranialis muscle BMC MUSCULOSKELETAL DISORDERS,9 2008 Author:Yuasa, Katsutoshi; Nakamura, Akinori; Hijikata, Takao; Takeda, Shinichi;
Follow-up of three cases with large in-frame deletion of exons 45-55 in the duchenne muscular dystrophy (DMD) Gene J Clin Nerosci,15:757-763 2008 Author:Nakamura A, Yoshida K, Fukushima K, Urasawa N, Ueda H, Koyama J, Yazaki Y, Takeda S, Ikeda S
Fiber type composition of diaphragm is more greatly influenced by dystrophin-deficiency in canine X-linked muscular dystrophy in Japan (CXMDJ), than that of limb skeletal muscle BMC Musculoskeletal Disorders,9:1 2008 Author:Yuasa K, Nakamura A, Hijikata T, Takeda S
Transduction profiles and immune response in the dystrophic dogs with rAAV serotype 8 HUMAN GENE THERAPY,18(10):984-985 2007(Oct.) Author:Ohshima, Sachiko; Shin, Jin-Hong; Nishiyama, Akiyo; Yuasa, Katsutoshi; Nakamura, Akinori; Nakai, Hiroyuki; Okada, Takashi; Takeda, Shin'ichi;
Successful treatment with infliximab and low-dose methotrexate in a Japanese patient with familial Mediterranean fever INTERNAL MEDICINE,46(15):1247-1249 2007 Author:Nakamura, Akinori; Matsuda, Masayuki; Tazawa, Ko-ichi; Shimojima, Yasuhiro; Ikeda, Shu-ichi;
Activation and localization of matrix metalloproteinase-2 and-9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ) BMC MUSCULOSKELETAL DISORDERS,8 2007 Author:Fukushima, Kazuhiro; Nakamura, Akinori; Ueda, Hideho; Yuasa, Katsutoshi; Yoshida, Kunihiro; Takeda, Shin'ichi; Ikeda, Shu-ichi;
Mandibuloacral dysplasia and a novel LMNA mutationin in a woman with severe progressive skeletal changes AMERICAN JOURNAL OF MEDICAL GENETICS PART A,143A(21):2598-2603 2007 Author:Kosho, Tomoki; Takahashi, Jun; Momose, Takashige; Nakamura, Akinori; Sakurai, Akihiro; Wada, Takahito; Yoshida, Kunihiro; Wakui, Keiko; Suzuki, Takefumi; Kasuga, Kazuo; Nishimura, Gen; Kato, Hiroyuki; Fukushima, Yoshimitsu;
Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ) BMC Musculoskeletal Disorders,8:54 2007 Author:Fukushima K, Nakamura A, Wada MR, Ueda H, Yuasa K, Yoshida K, Takeda S, Ikeda S
Intramuscular injection of a recombinant adeno-associated virus into canine skeletal muscle evoked immune resonses against products more susceptibility than that into murine muscles Gene Ther,14:1249-1260 2007 Author:Yuasa K, Yoshimura M, Urasawa N, Ohshima S, Sato K, Mochizuki Y, Yugeta N, Howell JM, Nakamura A, Hijikata T, Miyagoe-Suzuki Y, Takeda S
Cardiac involvements of beagle-based canine X-linked muscular dystrophy in Japan (CXMDJ): electrocardiographic, echocardiographic, and morphologic studies BMC Musculoskeletal Disorders,8:54 2007 Author:Fukushima K, Nakamura A, Wada MR, Ueda H, Yuasa K, Yoshida K, Takeda S, Ikeda S
A recombinant AAV-mediated gene transfer into canine skeletal muscle JOURNAL OF GENE MEDICINE,8(12):1459-1459 2006(Dec.) Author:Ohshima, Sachiko; Nishiyama, Akiyo; Yuasa, Katsutoshi; Nakamura, Akinori; Yoshimura, Madoka; Miyagoe-Suzuki, Yuko; Nakai, Hiroyuki; Takeda, Shin'ichi;
Coexistence of familial Mediterranean fever and Behcet's disease in a Japanese patient INTERNAL MEDICINE,45(12):799-800 2006 Author:Matsuda, Masayuki; Nakamura, Akinori; Tsuchiya, Saiko; Yoshida, Takuhiro; Horie, Shiro; Ikeda, Shu-ichi;
Non-episodic angioedema with eosinophilia: a report two cases and review of the literature Clin Rheumatol,25:422-425 2006 Author:Matsuda, Fushimi T, Nakamura A, Ikeda S
Major clinical and histopathological characteristics of canine X-linked muscular dystrophy in Japan, CXMDJ Acta Myologica,24:145-154 2005 Author:Shimatsu Y, Yoshimura M, Yuasa K, Urasawa N, Tomohiro M, Nakura M, Tanigawa M, Nakamura A, Takeda S
Severe protein losing enteropathy with intractable diarrhea due to systemic AA amyloidosis, successfully treated with corticosteroid and octreotide Amyloid: Int J Exp Clin Invest,12:48-53 2005 Author:Fushimi T, Takahashi Y, Kashima Y, Fukushima K, Ishii W, Kaneko K, Yazaki M, Nakamura A, Tokuda T, Matsuda M, Furuya R, Ikeda S
A Japanese case of familial Mediterranean fever with homozygosity for the pyrin E148Q mutation Internal Med,44:765-766 2005 Author:Suzuki T, Nakamura A, Yazaki M, Ikeda S
Physical exercise accelerates degeneration/regeneration cycle and down-regulated insulin-like growth factor-1 in dystrophin-deficient muscle Muscle Nerve,32:191-199 2005 Author:Okano T, Yoshida K, Nakamura A, Sasazawa F, Takeda S, Ikeda S
Unilateral oculomotor nerve palsy induced by combination therapy of interferon-a2b and ribavirin Internal Med,44:682-683 2005 Author:Nakamura A, Tojo K, Takasu K, Kaneko K, Komatsu H, Ikeda S
Increase in incidence of elderly-onset patients with myasthenia gravis in the Nagano distinct, Japan Internal Med,44:572-577 2005 Author:Matsuda M, Iijima-Dohi N, Nakamura A, Sekijima Y, Morita H, Sato S, Yahikozawa H, Tabata K, Yanagawa S, Ikeda S
A Japanese patient with familial Mediterranean fever, associated with compound heterozygosity for pyrin variant E148Q/M694I Internal Med,44:261-265 2005 Author:Nakamura A, Yazaki M, Tokuda T, Hattori T, Ikeda S
Up-regulation of mitogen activated protein kinase in mdx skeletal musclefollowing chronic treadmill exercise Biochim Biophys Acta,1740:326-331 2005 Author:Nakamura A, Yoshida K, Ueda H, Takeda S, Ikeda S
Neuregulin receptor ErbB2 localization at t-tubule in cardiac and skeletal muscle J Histochem Cytochem,53:87-91 2005 Author:Ueda H, Oikawa A, Nakamura A, Terasawa F, Moriizumi T
Caveolin-3 at the t-tubule colocalizes with a-actinin in adult murine cardiac muscle Acta Histochem Cytochem,37:373-378 2004 Author:Ueda H, Kawagishi K,Terasawa F, Nakamura A, Moriizumi T
Endotherial nitric oxide synthase expression in the sarcoplasimic reticule of mouse skeletal muscle Acta Histochem Cytochem,37:307-311 2004 Author:Kawagishi K, Terasawa F, Nakamura A, Moriizumi T, Ueda H
Nuclear envelope breakdown is a prominent feature is spinal motor neurons of wasted mice Acta Histochem Cytochem,37:159-162 2004 Author:Ueda H, Tezuka H, Nakamura A
Retrospective anlyses of clinical features and therapeutic outcomes in thymectomized patients with myasthenia gravis at Shinshu University Internal Med,43:189-193 2004 Author:Iijima-Dohi N, Sekjima Y, Nakamura A, Morita H, Matsuda M, Haniuda M, Hashimoto T, Ikeda S
Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles Clin Neruol Neurosurg,106:122-128 2004 Author:Nakamura A, Yoshida K, Ikeda S
Abdominal fat aspiration biopsy and genotyping of serum amyloid A contribute to early diagnosis of reactive AA amyloidosis secondary to rheumatoid arthritis Clin Neruol Neurosurg,106:122-128 2004 Author:Nakamura A, Yoshida K, Ikeda S
Usefulness of [123I]metaiodobenzylguanidine ([123I]MIBG) myocardial scintigraphy in differentiating between Altzheimer’s disease and dementia with Lewy bodies Internal Med,42:686-690 2003 Author:Oide T, Tokuda T, Momose M, Oguchi K, Nakamura A, Ohara S, Ikeda S
Progression of dystrophic features and activation of mitogen activated protein kinases and calcineurine in mdx heart by exercise FEBS Letters,520:18-24 2002 Author:Nakamura A, Yoshida K, Takeda S, Dohi N, Ikeda S
Non-herpetic fluminant meningoencephalitis with periodic lateralized epileptiform discharges J Clin Nerosci,9:190-192 2002 Author:Nakamura A, Hashimoto T, Shimada K, Matsuda M, Yanagisawa N
Life-threatening orthostatic hypotension in acase with bulbo-myelo-radiculo-neruopathy Autonomic Neuroscience: Basic& Clinical,94:125-131 2001 Author:Ishikawa S, Hattori T, Takei Y, Morita H, Yazaki M, Nakamura A, Ikeda S
Sterotyped stepping associated with lesions in the bilateral medial frontoparietal cortices Neurology,57:711-713 2001 Author:Sato, Hashimoto T, Nakamura A, Ikeda S
Activation of calcineurin and stress activated protein kinase/p38 mitogen activated protein kinase in hearts of utrophin-dystrophin knockout mice Neuromuscl Disord,11:251-259 2001 Author:NakamuraA, Harrod GV, Davies KE
Cessation of cerebral hemorrhage recurrence associated with corticosteroid treatment in a patient with cerebral amyloid angiopathy Amyloid: Int J Exp Clin Invest,7:284-288 2000 Author:Hoshi K, Yoshida K, Nakamura A, Tada T, Tamaoka A, Ikeda S
A case of pectoral fasciitis with spontaneous remission Eur Neurol,44:124-125 2000 Author:Fushimi T, Nakamura A, Yazaki M, Shimizu Y, Morita H, Ikeda S
Simultaneous exacerbation and remission of central and peripheral demyleination Muscle Nerve,23:440-441 2000 Author:Sato S, Nakamura A, Iwahashi T, Morita H, Hashimoto T, Ikeda S
Increased lipid peroxidation in the brains of aceruloplasminemia patients J Neruol Sci,175:91-95 2000 Author:Yoshida K, Kaneko K, Miyajima H, Tokuda T, Nakamura A, Kato M, Ikeda S
Clnical characteristics of aged Becker muscular dystrophy patients with onset after 30 years Eur Neurol,42:145-149 1999 Author:Yazaki M, Yoshida M, Nakamaura A, Koyama J, Nanba T, Ohori N, Ikeda S
A novel frame shift mutation in the McLeod syndrome gene in a Japanese family J Neruol Sci,165:6-9 1999 Author:Hanaoka N, Yoshida K, Nakamura A, Furihata K, Seo T, Tani Y, Takahashi J, Ikeda S, Hanyu N
Systemic sarcoidosis: a case with a focal hydrocephalus and elevated lysozyme and angitensin-converting enzyme in the cerebrospinal fluid J Neurol,246:320-322 1999 Author:Nakamura A, Ohara S, Maruyama K, Takei Y, Shindo M, Yanagisawa N
A novel SacI RFLP in the 3’ untranslated region of the myotonin protein kinase gene J Hum Genet,44:137-137 1999 Author:Nakamura A, Minami N, Kamitani T, Kamakura K, Arahata K, Takeda S
Insertional mutation by transposable element. L1, in the DMD gene results in X-liked dilated cardiomyopathy Hum Mol Genet,7:129-132 1998 Author:Yoshida K, Nakamura A, Yazaki M, Ikeda S, Takeda S
A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis J Nerol Sci,156:30-34 1998 Author:Yazaki M, Yoshida K, Nakamura A, Yonekawa M, Okabe T, Yamashita N, Ohta M, Ikeda S
Up-regulation of the brain and Purkinje-cell forms of dystrophin transcripts, in the Becker muscular dystrophy Am J Hum Genet,60:1555-1558 1997 Author:Nakamura A, Ikeda S, Yazaki M, Yoshida K, Kobayashi O, Yanagisawa N, Takeda S
Transthyretin Met 30 familial amyloid polyneuropathy in China: usefulness of mass spectrometry for screening a variant TTR in serum Amyloid: Int J Exp Clin Invest,4:104-107 1997 Author:Ikeda S, Tokuda T, Nakamura A, Ueno I, Taketomi T, Yanagisawa N, Li YF
大量飲酒後に発症し来院時高ナトリウム血症が確認されたcentral pontine and extra-pontine myelinolysisの一例 豊科赤十字病院医報,4:16-19 1996 Author:中野武、中村昭則
Reduction of serum IgG level and peripheral T-cell counts are correlated with CTG repeat lengths in myotonic dystrophy patients Neuromuscl Disord,6:203-210 1996 Author:Nakamura A, Kojo T, Arahata K, Takeda S
Myotonia congenital with painful muscle cramps Internal Med,6:507-511 1996 Author:Sunohara N, Tomi H, Nakamura A, Arahata K, Nonaka I
A mutation in the ceruloplasimin gene is associated with systemic hemosiderosis in humans Nature Genet,9:262-267 1995 Author:Yoshida K, Furihata K, Takeda S, Nakamura A, Yamamoto K, Morita H, Hiyamuta S, Ikeda S, Shimizu N, Yanagisawa N
DNA rearrangement in Japanese fascioscaplohumeral muscular dystrophy patients: clinical correlations Neuomuscl Disord,5:201-208 1995 Author:Goto K, Lee JH, Matsuda C, Hirabayashi K, Kojo T, Nakamura A, Mitsunaga Y, Furukawa T, Sahashi K, Arahata K
Decreased myotonin-protein kinase in the skeletal and cardiac muscle in myotonic dystrophy Biochem Biophys Res Comm,5:577-585 1994 Author:Koga R, Nakano Y, Kurano Y, Tsukahara T, Nakamura A, Ishiura S, Nonaka I, Arahata K
Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy. Muscle Nerve,16:1161-1166 1993 Author:Yoshida K, Ikeda S, Nakamura A, Kagoshima M, Takeda S, Shoji S, Yanagisawa N
末梢性顔面神経麻痺および前庭神経障害を合併したTolosa-Hunt症候群の一例 Brain and Nerve,44:655-659 1992 Author:大窪勝一郎、徳田隆彦、中村昭則、橋本隆男、高昌星、柳澤信夫
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学術論文査読件数 Lancet Lancet Neurology Human Molecular Genetics American Journal of Pathology Journal of Human Genetics Modern Rheumatology PLoS One FEBS Letters Molecules Internal Medicine Experimental Animals Tohoku Journal of Experimental Medicine Neuromuscular Disorders Muscle and Nerve BioMed International
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