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Movement Disorders (revue) - Curation (Accueil)

Index « AffRegInc.i » - entrée « Aichi »
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Ahaia < Aichi < Aix‐en‐Provence  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 6.
Ident.Authors (with country if any)Title
001768 (2011) Morinobu Seki [Japon] ; Kazushi Takahashi [Japon] ; Atsuo Koto [Japon] ; Ban Mihara [Japon] ; Yoko Morita [Japon] ; Kazuo Isozumi [Japon] ; Kouichi Ohta [Japon] ; Kazuhiro Muramatsu [Japon] ; Jun Gotoh [Japon] ; Keiji Yamaguchi [Japon] ; Yutaka Tomita [Japon] ; Hideki Sato [Japon] ; Yoshihiro Nihei [Japon] ; Satoko Iwasawa [Japon] ; Norihiro Suzuki [Japon]Camptocormia in Japanese patients with Parkinson's disease: A multicenter study
002568 (2008) Masaaki Hirayama [Japon] ; Tomohiko Nakamura [Japon] ; Norio Hori [Japon] ; Yasuo Koike [Japon] ; Gen Sobue [Japon]The video images of sleep attacks in Parkinson's disease
002F59 (2007) Hiroaki Nozaki [Japon] ; Takeshi Ikeuchi [Japon] ; Akio Kawakami [Japon] ; Akio Kimura [Japon] ; Reiji Koide [Japon] ; Miyuki Tsuchiya [Japon] ; Yuusaku Nakmura [Japon] ; Tatsuro Mutoh [Japon] ; Hiroko Yamamoto [Japon] ; Naoki Nakao [Japon] ; Ko Sahashi [Japon] ; Masatoyo Nishizawa [Japon] ; Osamu Onodera [Japon]Clinical and genetic characterizations of 16q‐linked autosomal dominant spinocerebellar ataxia (AD‐SCA) and frequency analysis of AD‐SCA in the Japanese population
003527 (2006) Hiroyuki Tomiyama [Japon] ; Yuanzhe Li [Japon] ; Manabu Funayama [Japon] ; Kazuko Hasegawa [Japon] ; Hiroyo Yoshino [Japon] ; Shin-Ichiro Kubo [Japon] ; Kenichi Sato [Japon] ; Tatsuya Hattori [Japon] ; Chin-Song Lu [Taïwan] ; Rivka Inzelberg [Israël] ; Ruth Djaldetti [Israël] ; Eldad Melamed [Israël] ; Rim Amouri [Tunisie] ; Neziha Gouider-Khouja [Tunisie] ; Faycal Hentati [Tunisie] ; Yasuko Hatano [Japon] ; Mei Wang [Japon] ; Yoko Imamichi [Japon] ; Koichi Mizoguchi [Japon] ; Hiroaki Miyajima [Japon] ; Fumiya Obata [Japon] ; Tatsushi Toda [Japon] ; Matthew J. Farrer [États-Unis] ; Yoshikuni Mizuno [Japon] ; Nobutaka Hattori [Japon]Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
003E15 (2004) Akio Kikuchi [Japon] ; Atsushi Takeda [Japon] ; Kazuo Fujihara [Japon] ; Teiko Kimpara [Japon] ; Yusei Shiga [Japon] ; Hiroaki Tanji [Japon] ; Makiko Nagai [Japon] ; Hiroshi Ichinose [Japon] ; Fumi Urano [Japon] ; Nobuyuki Okamura [Japon] ; Hiroyuki Arai [Japon] ; Yasuto Itoyama [Japon]Arg(184)his mutant GTP cyclohydrolase I, causing recessive hyperphenylalaninemia, is responsible for dopa‐responsive dystonia with parkinsonism: A case report
004A31 (2000) Ikuko Mizuta [Japon] ; Eiji Mizuta [Japon] ; Shunzou Yamasaki [Japon] ; Sadako Kuno [Japon] ; Minoru Yasuda [Japon] ; Chikako Tanaka [Japon]Meta‐analysis of polymorphism of the catechol‐O‐methyltransferase gene in relation to the etiology of Parkinson's disease in Japan

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