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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1965 2
1967 1
1968 2
1971 3
1973 1
1983 1
1984 1
1985 1
1986 4
1987 3
1988 1
1989 1
1991 1
1993 1
1994 6
1995 3
1996 4
1997 4
1998 5
1999 6
2000 4
2001 9
2002 2
2003 7
2004 2
2005 6
2006 10
2007 12
2008 19
2009 9
2010 10
2011 8
2012 20
2013 16
2014 17
2015 20
2016 17
2017 15
2018 20
2019 20
2020 20
2021 24
2022 19
2023 23
2024 19
2025 13

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361 results

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Page 1
Propagative α-synuclein seeds as serum biomarkers for synucleinopathies.
Okuzumi A, Hatano T, Matsumoto G, Nojiri S, Ueno SI, Imamichi-Tatano Y, Kimura H, Kakuta S, Kondo A, Fukuhara T, Li Y, Funayama M, Saiki S, Taniguchi D, Tsunemi T, McIntyre D, Gérardy JJ, Mittelbronn M, Kruger R, Uchiyama Y, Nukina N, Hattori N. Okuzumi A, et al. Among authors: funayama m. Nat Med. 2023 Jun;29(6):1448-1455. doi: 10.1038/s41591-023-02358-9. Epub 2023 May 29. Nat Med. 2023. PMID: 37248302 Free PMC article.
A rotarod test for evaluation of motor skill learning.
Shiotsuki H, Yoshimi K, Shimo Y, Funayama M, Takamatsu Y, Ikeda K, Takahashi R, Kitazawa S, Hattori N. Shiotsuki H, et al. Among authors: funayama m. J Neurosci Methods. 2010 Jun 15;189(2):180-5. doi: 10.1016/j.jneumeth.2010.03.026. Epub 2010 Mar 30. J Neurosci Methods. 2010. PMID: 20359499
[Pica].
Funayama M. Funayama M. Brain Nerve. 2018 Nov;70(11):1173-1180. doi: 10.11477/mf.1416201162. Brain Nerve. 2018. PMID: 30416110 Japanese.
Corrigendum.
Funayama M. Funayama M. Mov Disord. 2020 Nov;35(11):2127. doi: 10.1002/mds.28327. Mov Disord. 2020. PMID: 33463745 No abstract available.
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, Kasten M, Brüggemann N, Borsche M, Foroud T, Tolosa E, Garrido A, Annesi G, Gagliardi M, Bozi M, Stefanis L, Ferreira JJ, Correia Guedes L, Avenali M, Petrucci S, Clark L, Fedotova EY, Abramycheva NY, Alvarez V, Menéndez-González M, Jesús Maestre S, Gómez-Garre P, Mir P, Belin AC, Ran C, Lin CH, Kuo MC, Crosiers D, Wszolek ZK, Ross OA, Jankovic J, Nishioka K, Funayama M, Clarimon J, Williams-Gray CH, Camacho M, Cornejo-Olivas M, Torres-Ramirez L, Wu YR, Lee-Chen GJ, Morgadinho A, Pulkes T, Termsarasab P, Berg D, Kuhlenbäumer G, Kühn AA, Borngräber F, de Michele G, De Rosa A, Zimprich A, Puschmann A, Mellick GD, Dorszewska J, Carr J, Ferese R, Gambardella S, Chase B, Markopoulou K, Satake W, Toda T, Rossi M, Merello M, Lynch T, Olszewska DA, Lim SY, Ahmad-Annuar A, Tan AH, Al-Mubarak B, Hanagasi H, Koziorowski D, Ertan S, Genç G, de Carvalho Aguiar P, Barkhuizen M, Pimentel MMG, Saunders-Pullman R, van de Warrenburg B, Bressman S, Toft M, Appel-Cresswell S, Lang AE, Skorvanek M, Boon AJW, Krüger R, Sammler EM, Tu… See abstract for full author list ➔ Vollstedt EJ, et al. Among authors: funayama m. Mov Disord. 2023 Feb;38(2):286-303. doi: 10.1002/mds.29288. Epub 2023 Jan 24. Mov Disord. 2023. PMID: 36692014 Free article.
Pathological collecting behavior.
Funayama M, Takata T, Kato M, Mimura M. Funayama M, et al. Cortex. 2018 Jul;104:124-126. doi: 10.1016/j.cortex.2018.02.014. Epub 2018 Mar 3. Cortex. 2018. PMID: 29571960 No abstract available.
CHCHD2 P14L, found in amyotrophic lateral sclerosis, exhibits cytoplasmic mislocalization and alters Ca2+ homeostasis.
Ikeda A, Meng H, Taniguchi D, Mio M, Funayama M, Nishioka K, Yoshida M, Li Y, Yoshino H, Inoshita T, Shiba-Fukushima K, Okubo Y, Sakurai T, Amo T, Aiba I, Saito Y, Saito Y, Murayama S, Atsuta N, Nakamura R, Tohnai G, Izumi Y, Morita M, Tamura A, Kano O, Oda M, Kuwabara S, Yamashita T, Sone J, Kaji R, Sobue G, Imai Y, Hattori N. Ikeda A, et al. Among authors: funayama m. PNAS Nexus. 2024 Jul 30;3(8):pgae319. doi: 10.1093/pnasnexus/pgae319. eCollection 2024 Aug. PNAS Nexus. 2024. PMID: 39131911 Free PMC article.
[De Clérambault's erotomania].
Hamada H, Funayama M. Hamada H, et al. Among authors: funayama m. Ryoikibetsu Shokogun Shirizu. 2003;(38):132-5. Ryoikibetsu Shokogun Shirizu. 2003. PMID: 12876948 Review. Japanese. No abstract available.
Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease.
Tezuka T, Ishiguro M, Taniguchi D, Osogaguchi E, Shiba-Fukushima K, Ogata J, Ishii R, Ikeda A, Li Y, Yoshino H, Matsui T, Kaida K, Funayama M, Nishioka K, Kumazawa F, Matsubara T, Tsuda H, Saito Y, Murayama S, Imai Y, Hattori N. Tezuka T, et al. Among authors: funayama m. Neurobiol Dis. 2024 Sep;199:106571. doi: 10.1016/j.nbd.2024.106571. Epub 2024 Jun 18. Neurobiol Dis. 2024. PMID: 38901781 Free article.
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: funayama m. Mov Disord. 2023 Dec;38(12):2249-2257. doi: 10.1002/mds.29610. Epub 2023 Nov 5. Mov Disord. 2023. PMID: 37926948 Free PMC article.
361 results