Search Results - "Momose, Yoshio"

Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms by Momose, Yoshio, Murata, Miho, Kobayashi, Kazuhiro, Tachikawa, Masaji, Nakabayashi, Yuko, Kanazawa, Ichiro, Toda, Tatsushi

“…We studied 20 single nucleotide polymorphisms in 18 candidate genes for association with Parkinson's disease. We found that homozygosity for the V66M…”
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Appropriate data cleaning methods for genome-wide association study by Miyagawa, Taku, Nishida, Nao, Ohashi, Jun, Kimura, Ryosuke, Fujimoto, Akihiro, Kawashima, Minae, Koike, Asako, Sasaki, Tsukasa, Tanii, Hisashi, Otowa, Takeshi, Momose, Yoshio, Nakahara, Yasuo, Gotoh, Jun, Okazaki, Yuji, Tsuji, Shoji, Tokunaga, Katsushi

“…Genome-wide association studies (GWAS) using a large number of single nucleotide polymorphisms (SNPs) have successfully been applied to identify genetic…”
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Congenital long QT syndrome presenting with a history of epilepsy: Misdiagnosis or relationship between channelopathies of the heart and brain? by Omichi, Chikaya, Momose, Yoshio, Kitahara, Shigemi

“…Summary A 60‐year‐old man with a long history of epilepsy was referred for cardiologic evaluation. An earlier diagnosis of epilepsy was made on the basis of…”
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Alien hand sign observed at the initial stage of a case of Creutzfeldt-Jakob disease by Hashimoto, Meiko, Shimizu, Jun, Shirota, Yuichiro, Momose, Yoshio, Goto, Jun, Takeda, Katsuhiko, Tsuji, Shoji

“…A 68-year-old man was admitted to our hospital in the mid-October of 2006 because of a one-month history of peculiar movements of the left hand, which had been…”
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Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation by Iizuka, Takahiro, Takahashi, Yuji, Sato, Mayumi, Yonekura, Junko, Miyakawa, Saori, Endo, Motoi, Hamada, Junichi, Kan, Shinichi, Mochizuki, Hideki, Momose, Yoshio, Tsuji, Shoji, Sakai, Fumihiko

“…ObjectivesTo report cerebral blood flow changes during attacks of hemiplegic migraine with prolonged aura (HMPA) longer than 24 h in patients with familial…”
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Multiple candidate gene analysis identifies α-synuclein as a susceptibility gene for sporadic Parkinson's disease by Mizuta, Ikuko, Satake, Wataru, Nakabayashi, Yuko, Ito, Chiyomi, Suzuki, Satoko, Momose, Yoshio, Nagai, Yoshitaka, Oka, Akira, Inoko, Hidetoshi, Fukae, Jiro, Saito, Yuko, Sawabe, Motoji, Murayama, Shigeo, Yamamoto, Mitsutoshi, Hattori, Nobutaka, Murata, Miho, Toda, Tatsushi

“…Parkinson's disease (PD), one of the most common human neurodegenerative diseases, is characterized by the loss of dopaminergic neurons in the substantia nigra…”
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A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype-phenotype correlations by Kubota, Akatsuki, Hida, Ayumi, Ichikawa, Yaeko, Momose, Yoshio, Goto, Jun, Igeta, Yukifusa, Hashida, Hideji, Yoshida, Kunihiro, Ikeda, Syu-Ichi, Kanazawa, Ichiro, Tsuji, Shoji

“…Neuroferritinopathy is a hereditary neurodegenerative disorder caused by mutations in the ferritin light chain gene (FTL1). The cardinal features are…”
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Impact of Pharmacists' audit on improving the quality of prescription of dabigatran etexilate methanesulfonate: a retrospective study by Shimizu, Teppei, Momose, Yoshio, Ogawa, Ryuichi, Takahashi, Masahiro, Echizen, Hirotoshi

“…Appropriate prescription of dabigatran etexilate methanesulfonate (JAN) is more complicated than assumed, because there are totally 10 items of…”
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Toward identification of susceptibility genes for sporadic Parkinson's disease by Toda, Tatsushi, Momose, Yoshio, Murata, Miho, Tamiya, Gen, Yamamoto, Mitsutoshi, Hattori, Nobutaka, Inoko, Hidetoshi

“…To identify susceptibility genes for Parkinson's disease (PD) and to establish tailor-made medicine for PD, we studied 20 single nucleotide polymorphisms…”
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Attitude of outpatients with neuromuscular diseases in Japan to pain and use of analgesics by Abe, Yoshiki, Miyashita, Mitsunori, Ito, Naomi, Shirai, Yuki, Momose, Yoshio, Ichikawa, Yaeko, Tsuji, Shoji, Kazuma, Keiko

“…Abstract The prevalence of pain and its impact on outpatients with neuromuscular disease, and their attitude towards the use of analgesics were studied…”
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Orthostatic transient unresponsiveness in an elderly patient with severe cerebral arteriosclerosis under antihypertensive medication by Ohshita, T, Momose, Y, Kita, Y, Bando, M, Nagura, H, Yamanouchi, H

“…An 80-year-old man who had was administered antihypertensive medication showed repeated transient unresponsiveness during standing and/or walking. Neurological…”
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Multiplex families with multiple system atrophy by Hara, Kenju, Momose, Yoshio, Tokiguchi, Susumu, Shimohata, Mitsuteru, Terajima, Kenshi, Onodera, Osamu, Kakita, Akiyoshi, Yamada, Mitsunori, Takahashi, Hitoshi, Hirasawa, Motoyuki, Mizuno, Yoshikuni, Ogata, Katsuhisa, Goto, Jun, Kanazawa, Ichiro, Nishizawa, Masatoyo, Tsuji, Shoji

“…Multiple system atrophy (MSA) has been considered a sporadic disease, without patterns of inheritance. To describe the clinical features of 4 multiplex…”
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Multiple candidate gene analysis identifies [alpha]-synuclein as a susceptibility gene for sporadic Parkinson's disease by Mizuta, Ikuko, Satake, Wataru, Nakabayashi, Yuko, Ito, Chiyomi, Suzuki, Satoko, Momose, Yoshio, Nagai, Yoshitaka, Oka, Akira, Inoko, Hidetoshi, Fukae, Jiro, Saito, Yuko, Sawabe, Motoji, Murayama, Shigeo, Yamamoto, Mitsutoshi, Hattori, Nobutaka, Murata, Miho

“…Parkinson's disease (PD), one of the most common human neurodegenerative diseases, is characterized by the loss of dopaminergic neurons in the substantia nigra…”
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Toward identification of susceptibility genes for sporadic Parkinson?s disease by Toda, Tatsushi, Momose, Yoshio, Murata, Miho, Tamiya, Gen, Yamamoto, Mitsutoshi, Hattori, Nobutaka, Inoko, Hidetoshi

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Association studies of multiple candidate genes for Parkinson's Disease using single nucleotide polymorphisms by Momose, Yoshio, Murata, Miho, Kobayashi, Kazuhiro, Tachikawa, Masaji, Nakabayashi, Yuko, Kanazawa, Ichiro, Toda, Tatsushi

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