Search Results - "Nishida, Yoshihiko"

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    Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation by Kamada, Masaki, Izumi, Yuishin, Ayaki, Takashi, Nakamura, Masataka, Kagawa, Seiko, Kudo, Eiji, Sako, Wataru, Maruyama, Hirofumi, Nishida, Yoshihiko, Kawakami, Hideshi, Ito, Hidefumi, Kaji, Ryuji

    Published in Neuropathology (01-02-2014)
    “…We performed clinicopathological analyses of two amyotrophic lateral sclerosis (ALS) patients with homozygous Q398X optineurin (OPTN) mutation. Clinically,…”
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    Phosphatidylinositol-4,5-bisphosphate is enriched in granulovacuolar degeneration bodies and neurofibrillary tangles by Nishikawa, Tomokazu, Takahashi, Tetsuya, Nakamori, Masahiro, Yamazaki, Yu, Kurashige, Takashi, Nagano, Yoshito, Nishida, Yoshihiko, Izumi, Yuishin, Matsumoto, Masayasu

    Published in Neuropathology and applied neurobiology (01-06-2014)
    “…Aims Among the pathological findings in Alzheimer's disease (AD), the temporal and spatial profiles of granulovacuolar degeneration (GVD) bodies are…”
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    Late-onset myasthenia gravis is predisposed to become generalized in the elderly by Sakai, Waka, Matsui, Naoko, Ishida, Mitsuyo, Furukawa, Takahiro, Miyazaki, Yoshimichi, Fujita, Koji, Miyamoto, Ryosuke, Yamamoto, Nobuaki, Sako, Wataru, Sato, Kenta, Kondo, Kazuya, Nishida, Yoshihiko, Mitsui, Takao, Izumi, Yuishin, Kaji, Ryuji

    Published in eNeurologicalSci (01-03-2016)
    “…The continuous increase in the number of patients presenting with late-onset myasthenia gravis (LOMG) underscores the need for a better understanding of the…”
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    Dysphagia in Parkinson's disease by Hisashi, Shinobu, Fukumitsu, Ryoko, Ishida, Mitsuyo, Nodera, Atsuko, Otani, Takahiro, Maruoka, Takahiro, Nakamura, Kazumi, Izumi, Yuishin, Kaji, Ryuji, Nishida, Yoshihiko

    Published in Rinsho shinkeigaku = Clinical neurology (31-08-2016)
    “…Although dysphagia is an important symptom associated with prognosis in patients with Parkinson's disease (PD), dysphagia tends to be overlooked until…”
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    Hyperexcitability as a potential cause for diffuse lower motor neuron loss in Isaacs’ syndrome by Furukawa, Takahiro, Nodera, Hiroyuki, Shimatani, Yoshimitsu, Watanabe, Osamu, Miyashiro, Ai, Mori, Atsuko, Matsui, Naoko, Nishida, Yoshihiko, Izumi, Yuishin, Kaji, Ryuji

    Published in Neurology and clinical neuroscience (01-09-2013)
    “…We present a patient who initially developed diffuse painful muscle cramps who had elevated antibodies against voltage‐gated potassium channel (VGKC) complex…”
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    Increased replication of HTLV-I in HTLV-I-associated myelopathy by Yoshida, M, Osame, M, Kawai, H, Toita, M, Kuwasaki, N, Nishida, Y, Hiraki, Y, Takahashi, K, Nomura, K, Sonoda, S

    Published in Annals of neurology (01-09-1989)
    “…To estimate the replication of the human T-cell leukemia virus type I (HTLV-I) in patients with HTLV-I-associated myelopathy (HAM), or tropical spastic…”
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    Randomized controlled trial of KW-6356 monotherapy in patients with early untreated Parkinson's disease by Maeda, Tetsuya, Kimura, Takashi, Sugiyama, Kenichiro, Yamada, Kana, Hiraiwa, Ren, Nishi, Masato, Hattori, Nobutaka

    Published in Parkinsonism & related disorders (01-12-2023)
    “…KW-6356 is a novel selective adenosine A receptor antagonist/inverse agonist. We evaluated the efficacy and safety of KW-6356 as monotherapy in patients with…”
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    Successful treatment of stiff person syndrome with sequential use of tacrolimus by Nakane, Shunya, Fujita, Koji, Shibuta, Yoshiko, Matsui, Naoko, Harada, Masafumi, Urushihara, Ryo, Nishida, Yoshihiko, Izumi, Yuishin, Kaji, Ryuji

    “…[...]intravenous Ig (400 mg/kg body weight/day) was administered for 5 days in case 1 ( figure 1 A), whereas the patient in case 2 underwent a course of three…”
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    Late-onset spastic paraplegia: Aberrant SPG11 transcripts generated by a novel splice site donor mutation by Kawarai, Toshitaka, Miyamoto, Ryosuke, Mori, Atsuko, Oki, Ryosuke, Tsukamoto-Miyashiro, Ai, Matsui, Naoko, Miyazaki, Yoshimichi, Orlacchio, Antonio, Izumi, Yuishin, Nishida, Yoshihiko, Kaji, Ryuji

    Published in Journal of the neurological sciences (15-12-2015)
    “…Abstract We identified a novel homozygous mutation in the splice site donor (SSD) of intron 30 (c.5866 + 1G > A) in consanguineous Japanese SPG11 siblings…”
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    Localization of myoglobin in human muscle cells by immunoelectron microscopy by Kawai, H, Nishino, H, Nishida, Y, Masuda, K, Saito, S

    Published in Muscle & nerve (01-02-1987)
    “…The localization of myoglobin in human skeletal muscle cell was studied by immunoelectron microscopy. The Fab'-horseradish peroxidase (HRP) conjugate was…”
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    Missense and Nonsense Mutations in the Lysosomal α-Mannosidase Gene (MANB) in Severe and Mild Forms of α-Mannosidosis by Gotoda, Yasuo, Wakamatsu, Nobuaki, Kawai, Hisaomi, Nishida, Yoshihiko, Matsumoto, Toshio

    Published in American journal of human genetics (01-10-1998)
    “…α-Mannosidosis is an autosomal recessive lysosomal-storage disorder caused by a deficiency of lysosomal α-mannosidase activity. This disease shows a wide range…”
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    Cardiac dysfunction with Becker muscular dystrophy by Saito, Miho, Kawai, Hisaomi, Akaike, Masashi, Adachi, Katsuhito, Nishida, Yoshihito, Saito, Shiro

    Published in The American heart journal (01-09-1996)
    “…Cardiac function was examined in 21 patients with Becker muscular dystrophy (BMD) and compared with 43 patients with Duchenne muscular dystrophy (DMD) and 37…”
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    Loss of postural reflexes in long-term occupational solvent exposure by Kuriwaka, Rika, Mitsui, Takao, Fujiwara, Soichiro, Nishida, Yoshihiko, Matsumoto, Toshio

    Published in European neurology (01-01-2002)
    “…Inhalation of organic solvents has long been known to damage various nervous systems, including cerebellum, brainstem, and pyramidal tract. However, little is…”
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