Papers - TAKASHIMA Hiroshi
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Koge J, Hayashi S, Murai H, Yokoyama J, Mizuno Y, Uehara T, Ueda N, Watanabe O, Takashima H, Kira J. . Morvan's syndrome and myasthenia gravis related to familial Mediterranean fever gene mutations. . Journal of Neuroinflammation13 ( 1 ) 68 - 68 2016.3Morvan's syndrome and myasthenia gravis related to familial Mediterranean fever gene mutations.Reviewed
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Higuchi Y, Hashiguchi A, Yuan J, Yoshimura A, Mitsui J, Ishiura H, Tanaka M, Ishihara S, Tanabe H, Nozuma S, Okamoto Y, Matsuura E, Ohkubo R, Inamizu S, Shiraishi W, Yamasaki R, Ohyagi Y, Kira J, Oya Y, Yabe H, Nishikawa N, Tobisawa S, Matsuda N, Masuda M, Kugimoto C, Fukushima K, Yano S, Yoshimura J, Doi K, Nakagawa M, Morishita S, Tsuji S, Takashima H. . Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2. . Annals of Neurology79 ( 4 ) 659 - 672 2016.3Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.Reviewed
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Adachi H, Ishihara K, Tachibana H, Oka N, Higuchi Y, Takashima H, Yoneda Y, Kageyama Y. . Adult-onset Krabbe disease presenting with an isolated form of peripheral neuropathy. . Muscle and Nerve 2016.2Adult-onset Krabbe disease presenting with an isolated form of peripheral neuropathy.Reviewed
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Nakazato Y, Mochizuki H, Ishii N, Ohkubo R, Hirano R, Takashima H, Shiomi K, Nakazato M. . Spinocerebellar ataxia 36 accompanied by cervical dystonia. . Journal of Neurological Science357 ( 1-2 ) 304 - 306 2015.10Spinocerebellar ataxia 36 accompanied by cervical dystonia.Reviewed
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Sakiyama Y, Kanda N, Higuchi Y, Yoshimura M, Wakaguri H, Takata Y, Watanabe O, Yuan J, Tashiro Y, Saigo R, Nozuma S, Yoshimura A, Arishima S, Ikeda K, Shinohara K, Arata H, Michizono K, Higashi K, Hashiguchi A, Okamoto Y, Hirano R, Shiraishi T, Matsuura E, Okubo R, Higuchi I, Goto M, Hirano H, Sano A, Iwasaki T, Matsuda F, Izumo S, Takashima H. . New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan. . Neurology Neuroimmunology and Neuroinflammation2 ( 5 ) e143 2015.8New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan.Reviewed
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Yoshinaga H, Sakoda S, Shibata T, Akiyama T, Oka M, Yuan JH, Takashima H, Takahashi MP, Kitamura T, Murakami N, Kobayashi K. . Phenotypic variability in childhood of skeletal muscle sodium channelopathies. . Pediatric Neurology52 ( 5 ) 504 - 508 2015.5Phenotypic variability in childhood of skeletal muscle sodium channelopathies.Reviewed
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Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, Goto J, Ichikawa Y, Nakahara Y, Momose Y, Takahashi Y, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Watanabe H, Ito M, Sobue G, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake W, Toda T, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Tanner CM, Kukull WA, Stern MB, Lee VM, Trojanowski JQ, Masliah E, Low PA, Sandroni P, Ozelius LJ, Foroud T, Tsuji S. . Variants associated with Gaucher disease in multiple system atrophy. . Annals of Clinical and Translational Neurology2 ( 4 ) 417 - 426 2015.4Variants associated with Gaucher disease in multiple system atrophy.Reviewed
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Matsuura E, Yoshimura A, Nozuma S, Higuchi I, Kubota R, Takashima H. . Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP). . BMC Neurology28 ( 15 ) 18 - 18 2015.2Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP).Reviewed
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Yuan J, Ando M, Higuchi I, Sakiyama Y, Matsuura E, Michizono K, Watanabe O, Nagano S, Inamori Y, Hashiguchi A, Higuchi Y, Yoshimura A, Takashima H. . Partial deficiency of emerin caused by a splice site mutation in EMD. . Intern Med. 53 ( 14 ) 1563 - 1568 2014.7Partial deficiency of emerin caused by a splice site mutation in EMD.Reviewed
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Furukawa Y, Hashiguchi T, Minami R, Yamamoto M, Takashima H. . Exacerbation of microcytic anemia associated with cessation of anti-retroviral therapy in an HIV-1-infected patient with beta thalassemia. . J Infect Chemother. 20 ( 6 ) 387 - 389 2014.6Exacerbation of microcytic anemia associated with cessation of anti-retroviral therapy in an HIV-1-infected patient with beta thalassemia.Reviewed
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Hiramatsu Y, Wakita M, Matsuoka H, Kasuya J, Hamada R, Takashima H. . Cerebral infarction associated with accessory middle cerebral arteries: two case reports. . Intern Med. 53 ( 12 ) 1381 - 1384 2014.6Cerebral infarction associated with accessory middle cerebral arteries: two case reports.Reviewed
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Nozuma S, Matsuura E, Matsuzaki T, Watanabe O, Kubota R, Izumo S, Takashima H. . Familial clusters of HTLV-1-associated myelopathy/tropical spastic paraparesis. . PLoS One. 9 ( 5 ) e86144 - e86144 2014.5Familial clusters of HTLV-1-associated myelopathy/tropical spastic paraparesis.Reviewed
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荒田仁、大窪隆一、渡邊修、髙嶋博、橋口照人 . 神経疾患ノバイオマーカーの新展開 . 日本内科学会雑誌102 ( 12 ) 3174 - 3182 2013.12神経疾患ノバイオマーカーの新展開Reviewed
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平野隆城、樋口雄二郎、西郷隆二、大窪隆一、髙嶋博 . 南九州地域の遺伝性脊髄小脳変性症 -疾患の特徴と遺伝子診断- . 神経内科78 ( 3 ) 257 - 264 2013.3南九州地域の遺伝性脊髄小脳変性症 -疾患の特徴と遺伝子診断-Reviewed
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出口尚寿、有村愛子、髙嶋博、西尾善彦 . 糖尿病性筋委縮症：病態と治療 . 糖尿病合併症27 ( 2 ) 173 - 177 2013.2糖尿病性筋委縮症：病態と治療Reviewed
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Inamori Y, Higuchi I, Inoue T, Sakiyama Y, Hashiguchi A, Higashi K, Shiraishi T, Okubo R, Arimura K, Mitsuyama Y, Takashima H . Inclusion body myositis coexisting with hypertrophic cardiomyopathy: An autopsy study. . Neuromuscul Disord22 ( 8 ) 747 - 754 2012.9 Inclusion body myositis coexisting with hypertrophic cardiomyopathy: An autopsy study.Reviewed
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Saiga T, Tateishi T, Torii T, Kawamura N, Nagara Y, Shigeto H, Hashiguchi A, Takashima H, Honda H, Ohyagi Y, Kira J. . Inflammatory radiculoneuropathy in an ALS4 patient with a novel SETX mutation. . J Neurol Neurosurg Psychiatry17 ( 2 ) 763 - 764 2012.7Inflammatory radiculoneuropathy in an ALS4 patient with a novel SETX mutation.Reviewed
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Zhao Z, Hashiguchi A, Hu J, Sakiyama Y, Okamoto Y, Tokunaga S, Zhu L, Shen H, Takashima H . Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy. . Neurology78 ( 21 ) 1644 - 1649 2012.5Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy. Reviewed
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Tomonori Nakamura, Akihiro Hashiguchi, Shinsuke Suzuki, Kimiharu Uozumi, Shoko Tokunaga, Hiroshi Takashima . Vincristine exacerbates asymptomatic Charcot-Marie-Toothdisease with a novel EGR2 mutation. . Neurogenetics13 ( 1 ) 77 - 82 2012.2Vincristine exacerbates asymptomatic Charcot-Marie-Toothdisease with a novel EGR2 mutation.Reviewed
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Kensuke Shiga, Yuichi Noto, Ikuko Mizuta, Akihiro Hashiguchi, Hiroshi Takashima, Masanori Nakagawa . A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth disease. . Journal of the Peripheral Nervous System17 ( 2 ) 206 - 209 2012.2A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth disease. Reviewed