1. A case of α‐synuclein gene duplication presenting with head‐shaking movements. Issue 3 (2nd November 2012) Authors: Itokawa, Kaori; Sekine, Takeshi; Funayama, Manabu; Tomiyama, Hiroyuki; Fukui, Miki; Yamamoto, Toshimasa; Tamura, Naotoshi; Matsuda, Hiroshi; Hattori, Nobutaka; Araki, Nobuo Journal: Movement disorders Issue: Volume 28:Issue 3(2013) Page Start: 384 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A metabolic profile of polyamines in parkinson disease: A promising biomarker. Issue 2 (1st July 2019) Authors: Saiki, Shinji; Sasazawa, Yukiko; Fujimaki, Motoki; Kamagata, Koji; Kaga, Naoko; Taka, Hikari; Li, Yuanzhe; Souma, Sanae; Hatano, Taku; Imamichi, Yoko; Furuya, Norihiko; Mori, Akio; Oji, Yutaka; Ueno, Shin‐Ichi; Nojiri, Shuko; Miura, Yoshiki; Ueno, Takashi; Funayama, Manabu; Aoki, Shigeki; Hattori... Journal: Annals of neurology Issue: Volume 86:Issue 2(2019) Page Start: 251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel mutation of CHCHD2 p.R8H in a sporadic case of Parkinson's disease. (January 2017) Authors: Ikeda, Aya; Matsushima, Takashi; Daida, Kensuke; Nakajima, Sho; Conedera, Silvio; Li, Yuanzhe; Yoshino, Hiroyo; Oyama, Genko; Funayama, Manabu; Nishioka, Kenya; Hattori, Nobutaka Journal: Parkinsonism & related disorders Issue: Volume 34(2017) Page Start: 66 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout. (19th January 2015) Authors: Matsuo, Hirotaka; Tomiyama, Hiroyuki; Satake, Wataru; Chiba, Toshinori; Onoue, Hiroyuki; Kawamura, Yusuke; Nakayama, Akiyoshi; Shimizu, Seiko; Sakiyama, Masayuki; Funayama, Manabu; Nishioka, Kenya; Shimizu, Toru; Kaida, Kenichi; Kamakura, Keiko; Toda, Tatsushi; Hattori, Nobutaka; Shinomiya, Nariy... Journal: Annals of clinical and translational neurology Issue: Volume 2:Number 3(2015:Mar.) Page Start: 302 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint‐like inclusion body formation, and selective degeneration of dopaminergic neurons. Issue 9 (13th March 2013) Authors: Matsui, Hideaki; Sato, Fumiaki; Sato, Shigeto; Koike, Masato; Taruno, Yosuke; Saiki, Shinji; Funayama, Manabu; Ito, Hidefumi; Taniguchi, Yoshihito; Uemura, Norihito; Toyoda, Atsushi; Sakaki, Yoshiyuki; Takeda, Shunichi; Uchiyama, Yasuo; Hattori, Nobutaka; Takahashi, Ryosuke Journal: FEBS letters Issue: Volume 587:Issue 9(2013) Page Start: 1316 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. CHCHD2 and Parkinson's disease—Authors' reply. Issue 7 (July 2015) Authors: Funayama, Manabu; Hattori, Nobutaka Journal: Lancet neurology Issue: Volume 14:Issue 7(2015:Jul.) Page Start: 682 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. Issue 3 (March 2015) Authors: Funayama, Manabu; Ohe, Kenji; Amo, Taku; Furuya, Norihiko; Yamaguchi, Junji; Saiki, Shinji; Li, Yuanzhe; Ogaki, Kotaro; Ando, Maya; Yoshino, Hiroyo; Tomiyama, Hiroyuki; Nishioka, Kenya; Hasegawa, Kazuko; Saiki, Hidemoto; Satake, Wataru; Mogushi, Kaoru; Sasaki, Ryogen; Kokubo, Yasumasa; Kuzuhara, ... Journal: Lancet neurology Issue: Volume 14:Issue 3(2015:Mar.) Page Start: 274 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. Issue 3 (March 2015) Authors: Funayama, Manabu; Ohe, Kenji; Amo, Taku; Furuya, Norihiko; Yamaguchi, Junji; Saiki, Shinji; Li, Yuanzhe; Ogaki, Kotaro; Ando, Maya; Yoshino, Hiroyo; Tomiyama, Hiroyuki; Nishioka, Kenya; Hasegawa, Kazuko; Saiki, Hidemoto; Satake, Wataru; Mogushi, Kaoru; Sasaki, Ryogen; Kokubo, Yasumasa; Kuzuhara, ... Journal: Lancet neurology Issue: Volume 14:Issue 3(2015:Mar.) Page Start: 274 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features. Issue 4 (17th February 2019) Authors: Ikeda, Aya; Shimada, Hitoshi; Nishioka, Kenya; Takanashi, Masashi; Hayashida, Arisa; Li, Yuanzhe; Yoshino, Hiroyo; Funayama, Manabu; Ueno, Yuji; Hatano, Taku; Sahara, Naruhiko; Suhara, Tetsuya; Higuchi, Makoto; Hattori, Nobutaka Journal: Movement disorders Issue: Volume 34:Issue 4(2019) Page Start: 568 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Clinical manifestations of Parkinson's disease harboring VPS35 retromer complex component p.D620N with long-term follow-up. (March 2021) Authors: Ishiguro, Mayu; Li, Yuanzhe; Yoshino, Hiroyo; Daida, Kensuke; Ishiguro, Yuta; Oyama, Genko; Saiki, Shinji; Funayama, Manabu; Hattori, Nobutaka; Nishioka, Kenya Journal: Parkinsonism & related disorders Issue: Volume 84(2021) Page Start: 139 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗