Mana Higashihara < Manabu Funayama < Manabu Honda

Facettes :

List of bibliographic references indexed by Manabu Funayama

Number of relevant bibliographic references: 12.

Ident.	Authors (with country if any)	Title
000B37 (2013)	Kaori Itokawa [Japon] ; Takeshi Sekine ; Manabu Funayama ; Hiroyuki Tomiyama ; Miki Fukui ; Toshimasa Yamamoto ; Naotoshi Tamura ; Hiroshi Matsuda ; Nobutaka Hattori ; Nobuo Araki	A case of α-synuclein gene duplication presenting with head-shaking movements.
000B59 (2012)	Maya Ando [Japon] ; Manabu Funayama ; Yuanzhe Li ; Kenichi Kashihara ; Yoshitake Murakami ; Nobutaka Ishizu ; Chizuko Toyoda ; Katsuhiko Noguchi ; Takashi Hashimoto ; Naoki Nakano ; Ryogen Sasaki ; Yasumasa Kokubo ; Shigeki Kuzuhara ; Kotaro Ogaki ; Chikara Yamashita ; Hiroyo Yoshino ; Taku Hatano ; Hiroyuki Tomiyama ; Nobutaka Hattori	VPS35 mutation in Japanese patients with typical Parkinson's disease.
000C45 (2012)	Manabu Funayama [Japon] ; Hiroyo Yoshino ; Yuanzhe Li ; Hiromichi Kusaka ; Hiroyuki Tomiyama ; Nobutaka Hattori	Pseudo-heterozygous rearrangement mutation of parkin.
000F37 (2012)	Maya Ando [Japon] ; Manabu Funayama [Japon] ; YUANZHE LI [Japon] ; Kenichi Kashihara [Japon] ; Yoshitake Murakami [Japon] ; Nobutaka Ishizu [Japon] ; Chizuko Toyoda [Japon] ; Katsuhiko Noguchi [Japon] ; Takashi Hashimoto [Japon] ; Naoki Nakano [Japon] ; Ryogen Sasaki [Japon] ; Yasumasa Kokubo [Japon] ; Shigeki Kuzuhara [Japon] ; Kotaro Ogaki [Japon] ; Chikara Yamashita [Japon] ; Hiroyo Yoshino [Japon] ; Taku Hatano [Japon] ; Hiroyuki Tomiyama [Japon] ; Nobutaka Hattori [Japon]	VPS35 Mutation in Japanese Patients with Typical Parkinson's Disease
001014 (2012)	Manabu Funayama [Japon] ; Hiroyo Yoshino [Japon] ; YUANZHE LI [Japon] ; Hiromichi Kusaka [Japon] ; Hiroyuki Tomiyama [Japon] ; Nobutaka Hattori [Japon]	Pseudo-heterozygous Rearrangement Mutation of parkin
001A66 (2010)	Manabu Funayama [Japon] ; Hiroyuki Tomiyama [Japon] ; Ruey-Meei Wu [Taïwan] ; Kotaro Ogaki [Japon] ; Hiroyo Yoshino [Japon] ; Yoshikuni Mizuno [Japon] ; Nobutaka Hattori [Japon]	Rapid screening of ATP13A2 variant with high‐resolution melting analysis
001D95 (2010)	Takeshi Sekine [Japon] ; Hajime Kagaya [Japon] ; Manabu Funayama [Japon] ; Yuanzhe Li [Japon] ; Hiroyo Yoshino [Japon] ; Hiroyuki Tomiyama [Japon] ; Nobutaka Hattori [Japon]	Clinical course of the first Asian family with Parkinsonism related to SNCA triplication
002122 (2009)	Kazuaki Kanai [Japon] ; Masato Asahina [Japon] ; Kimihito Arai [Japon] ; Hiroyuki Tomiyama [Japon] ; Yoichi Kuwabara [Japon] ; Tomoyuki Uchiyama [Japon] ; Yukari Sekiguchi [Japon] ; Manabu Funayama [Japon] ; Satoshi Kuwabara [Japon] ; Nobutaka Hattori [Japon] ; Takamichi Hattori [Japon]	Preserved cardiac 123I‐MIBG uptake and lack of severe autonomic dysfunction in a PARK9 patient
002747 (2008)	Hiroyuki Tomiyama [Japon] ; Yasumasa Kokubo [Japon] ; Ryogen Sasaki [Japon] ; Yuanzhe Li [Japon] ; Yoko Imamichi [Japon] ; Manabu Funayama [Japon] ; Yoshikuni Mizuno [Japon] ; Nobutaka Hattori [Japon] ; Shigeki Kuzuhara [Japon]	Mutation analyses in amyotrophic lateral sclerosis/parkinsonism–dementia complex of the Kii peninsula, Japan
002846 (2008)	Manabu Funayama [Japon] ; Yuanzhe Li [Japon] ; Tak-Hong Tsoi [République populaire de Chine] ; Ching-Wan Lam [République populaire de Chine] ; Takekazu Ohi [Japon] ; Shogo Yazawa [Japon] ; Eiichiro Uyama [Japon] ; Ruth Djaldetti [Israël] ; Eldad Melamed [Israël] ; Hiroyo Yoshino [Japon] ; Yoko Imamichi [Japon] ; Hiroshi Takashima [Japon] ; Kenya Nishioka [Japon] ; Kenichi Sato [Japon] ; Hiroyuki Tomiyama [Japon] ; Shin-Ichiro Kubo [Japon] ; Yoshikuni Mizuno [Japon] ; Nobutaka Hattori [Japon]	Familial Parkinsonism with digenic parkin and PINK1 mutations
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
003A47 (2005)	Etsuro Ohta [Japon] ; Itaru Toyoshima [Japon] ; Manabu Funayama [Japon] ; Hiroshi Ichinose [Japon] ; Kazuko Hasegawa [Japon] ; Fumiya Obata [Japon]	A new mutation (Thr106Ile) of the GTP cyclohydrolase 1 gene associated with DYT5 dystonia (Segawa disease)

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