パーキンソン病 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "パーキンソン病" in Japanese language version.

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Rao, Shobha S.; Hofmann, Laura A.; Shakil, Amer (2006), “Parkinson's disease: diagnosis and treatment”, Am Fam Physician 74: 2046-54, PMID 17186710 full text

afpbb.com

「医療用植物は世界に2万8000種超、大半が未活用英王立植物園」AFP（2017年5月18日）

agmc.hyogo.jp

“パーキンソン病の基礎知識と療養のポイント - 神経難病の知識”. agmc.hyogo.jp. 兵庫県難病相談センター. 2019年2月12日閲覧。

almediaweb.jp

“アキネジア :医療・ケア用語集”. アルメディアWEB. 2019年12月23日閲覧。

asahi.com

「パーキンソン病血液検査で判断たんぱく質の異常検出順天堂大など」『朝日新聞』朝刊2023年6月6日（社会・総合面）2023年6月10日閲覧
iPS治験が米でも開始へ　パーキンソン病対象、日本から細胞を空輸（朝日新聞、2023年12月26日）

boehringerplus.jp

パーキンソン病症状日誌ベーリンガーインゲルハイム

doi.org

Woulfe J, Hoogendoorn H, Tarnopolsky M, Muñoz DG (2000). "Monoclonal antibodies against Epstein-Barr virus cross-react with alpha-synuclein in human brain". Neurology. 55 (9): 1398-401., PMID 11087792, doi:10.1212/WNL.55.9.1398.
Yamawaki, M; Kusumi, M; Kowa, H; Nakashima, K (2009). “Changes in prevalence and incidence of Parkinson's disease in Japan during a quarter of a century”. Neuroepidemiology 32 (4): 263-269. doi:10.1159/000201565. PMID 19209006.
Haaxma CA, Bloem BR, Borm GF, Oyen WJ, Leenders KL, Eshuis S, Booij J, Dluzen DE, Horstink MW (Aug 2006). “Gender differences in Parkinson's disease” (full text). J Neurol Neurosurg Psychiatry 78 (8): 819-824. doi:10.1136/jnnp.2006.103788. PMID 17098842.
Dorsey, E. Ray et al. (Mar 2023). “Trichloroethylene: An Invisible Cause of Parkinson’s Disease?”. Journal of Parkinson's Disease 13 (2): 203-218. doi:10.3233/JPD-225047.
Knekt, Paul; Kilkkinen, Annamari; Rissanen, Harri; Marniemi, Jukka; Saaksjarvi, Katri; Heliovaara, Markku (2010). “Serum Vitamin D and the risk of Parkinson disease”. Arch Neurol 67 (7): 808-811. doi:10.1001/archneurol.2010.120.
Gagne, JJ; Power, MC (Mar 2010). “Anti-inflammatory drugs and risk of Parkinson disease: a meta-analysis”. Neurology 74 (12): 995-1002. doi:10.1212/WNL.0b013e3181d5a4a3. PMID 20308684.
中西亮二、山永裕明、野尻晋一、出田透「パーキンソン病の障害評価とリハビリテーション」 The Japanese Journal of Rehabilitation Medicine., 50巻 (2013) 8号 pp.658-670, doi:10.2490/jjrmc.50.658
Poewe, W (Feb 2009). “17”. Neurology 72 (7 Suppl): S65-73. doi:10.1212/WNL.0b013e31819908ce. PMID 19221317.
PD MED Collaborative Group. Long-term effectiveness of dopamine agonists and monoamine oxidase B inhibitors compared with levodopa as initial treatment for Parkinson's disease (PD MED): a large, open-label, pragmatic randomised trial. The Lancet, Early Online Publication, 11 June 2014. doi:10.1016/S0140-6736(14)60683-8
Seppi, K; Weintraub, D; Coelho, M; Perez-Lloret, S; Fox, SH; Katzenschlager, R; Hametner, EM; Poewe, W et al. (Oct 2011). “The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the non-motor symptoms of Parkinson's disease”. Mov Disord 26 Supple 3: S42-80. doi:10.1002/mds.23884. PMID 22021174.
Olanow, CW; Rascol, O; Hauser, R; Feigin, PD; Jankovic, J; Lang, A; Langston, W; Melamed, E et al.; ADAGIO Study Investigators (Sep 2009). “A double-blind, delayde-start trial of rasagiline in Parkinson's disease”. N Engl J Med 361 (13): 1268-1278. doi:10.1056/NEJMoa0809335. PMID 19776408.
Rascol, O; Fitzer-Attas, CJ; Hauser, R; Jankovic, J; Lang, A; Langston, JW; Melamed, E; Poewe, W et al. (May 2011). “A double-blind, delayed-start trial of rasagiline in Parkinson's disease (the ADAGIO study): prespecified and post-hoc analyses of the need for additional therapies, changes in UPDRS scores, and non-motor outcomes”. Lancet Neurol 10 (5): 415-423. doi:10.1016/S1474-4422(11)70073-4. PMID 21482191.
村田美穂「新しい抗パーキンソン病薬ゾニサミドの発見」『臨床神経学』第50巻第2号、2010年2月、67-73頁、doi:10.5692/clinicalneurol.50.67。
D, Devos (May 2009). format=full text “Patient profile, indications, efficacy and safety of duodenal levodopa infusion in advanced Parkinson's disease”. Mov Disord 24 (7): 993-1000. doi:10.1002/mds.22450. PMID 19253412.
Hickey, P; Stacy, M (2011). “Available and emerging treatments for Parkinson's disease: a review”. Drug design, development and therapy 5: 241-254. doi:10.2147/DDDT.S11836. PMID 21607020.
Bara-Jimenez, W; Sherzai, A; Dimirova, T; Favit, A; Bibbiani, F; Gillespie, M; Morris, MJ; Mouradian, MM et al. (August 2003). “Adenosine A_2A receptor antagonist treatment of Parkinson’s disease”. Neurology 61 (3): 293-296. doi:10.1212/01.WNL.0000073136.00548.D4. PMID 12913186.
Eggert K, Squillacote D, Barone P, Dodel R, Katzenschlager R, Emre M, Lees AJ, Rascol O, Poewe W, Tolosa E, Trenkwalder C, Onofrj M, Stocchi F, Nappi G, Kostic V, Potic J, Ruzicka E, Oertel W; German Competence Network on Parkinson's Disease (May 2010). “Safety and efficacy of perampanel in advanced Parkinson's disease: a randomized, placebo-controlled study”. Mov Disord 25 (7): 896-905. doi:10.1002/mds.22974. PMID 20461807.
Fahn S, Oakes D, Shoulson I, Kieburtz K, Rudolph A, Lang A, Olanow CW, Tanner C, Marek K; Parkinson Study Group (Dec 2004). “Levodopa and the progression of Parkinson's disease” (free full text). N Engl J Med 351 (24): 2498-2508. doi:10.1056/NEJMoa033447. PMID 15590952.
Shapira, AH; Olanow, CW (Dec 2008). “Drug selection and timing of initiation of treatment in early Parkinson's disease”. Ann Neurol 64 (Suppl2): S47-55. doi:10.1002/ana.21460. PMID 19127579.
村松慎一「パーキンソン病の遺伝子治療」『臨床神経学』第52巻第11号、日本神経学会、2012年、896-898頁、doi:10.5692/clinicalneurol.52.896、ISSN 0009-918X。
Hatano, T; Kubo, S; Sato, S; Hattori, N (Dec 2009). “Pathogenesis of familial Parkinson's disease: new insights based on monogenic forms of Parkinson's disease”. J Neurochem 111 (5): 1075-1093. doi:10.1111/j.1471-4159.2009.06403.x. PMID 19780902.
Singleton AB, Farrer M, Johnson J, et al (2003). “alpha-Synuclein locus triplication causes Parkinson's disease”. Science 302 (5646): 841. doi:10.1126/science.1090278. PMID 14593171.
Poorkaj P et al. (2004). “parkin mutation analysis in clinic patients with early-onset Parkinson's disease” (abstract page). American Journal of Medical Genetics Part A 129A (1): 44–50. doi:10.1002/ajmg.a.30157.
Ebba Lohmann et al. (2003). “How much phenotypic variation can be attributed to parkin genotype?” (abstract page). Annals of Neurology 54 (2): 176–185. doi:10.1002/ana.10613. PMID 12891670.
佐藤栄人「家族性パーキンソン病の分子病態を基盤としたバイオマーカーの検討」『臨床神経学』第52巻第11号、日本神経学会、2012年、1327-1328頁、doi:10.5692/clinicalneurol.52.1327、ISSN 0009-918X、PMID 23196607。
Okatsu K, Oka T, Iguchi M, Imamura K, Kosako H, Tani N, Kimura M, Go E, Koyano F, Funayama M, Shiba-Fukushima K, Sato S, Shimizu H, Fukunaga Y, Taniguchi H, Komatsu M, Hattori N, Mihara K, Tanaka K, Matsuda N (Aug 2012). “PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria” (free full text). Nat Commun 3: 1016. doi:10.1038/ncomms2016. PMC 3432468. PMID 22910362.
Imai, Y; Bingwei, L (Dec 2011). “Mitochondrial Dynamics and Mitophagy in Parkinson’s Disease: Disordered cellular power plant becomes a big deal in a major movement disorder” (free full text). Curr Opin Neurobiol 21 (6): 935-941. doi:10.1016/j.conb.2011.10.016. PMC 3254859. PMID 22048001.
Kim RH, Smith PD, Aleyasin H, Hayley S, Mount MP, Pownall S, Wakeham A, You-Ten AJ, Kalia SK, Horne P, Westaway D, Lozano AM, Anisman H, Park DS, Mak TW (Apr 2005). “Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) and oxidative stress”. Proc Natl Acad Sci U S A 102 (14): 5215-5220. doi:10.1073/pnas.0501282102. PMC 555037. PMID 15784737.
Irrcher I, Aleyasin H, Seifert EL, Hewitt SJ, Chhabra S, Phillips M, Lutz AK, Rousseaux MW, Bevilacqua L, Jahani-Asl A, Callaghan S, MacLaurin JG, Winklhofer KF, Rizzu P, Rippstein P, Kim RH, Chen CX, Fon EA, Slack RS, Harper ME, McBride HM, Mak TW, Park DS (Oct 2010). “Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics”. Hum Mol Genet 19 (19): 3734-3746. doi:10.1093/hmg/ddq288. PMID 20639397.
Smith WW, Pei Z, Jiang H, Moore DJ, Liang Y, West AB, Dawson VL, Dawson TM, Ross CA (2005). “Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration”. Proceedings of the National Academy of Sciences of the United States of America 102 (51): 18676–18681. doi:10.1073/pnas.0508052102. PMID 16352719.
Usenovic, M; Tresse, E; Mazzulli, JR; Taylor, JP; Krainc, D (Mar 2012). “Deficiency of ATP13A2 leads to lysosomal dysfunction, α-synuclein accumulation, and neurotoxicity” (free full text). J Neurosci 32 (12): 4240-4246. doi:10.1523/JNEUROSCI.5575-11.2012. PMID 22442086.
Lautier C, Goldwurm S, Durr A, Giovannone B, Tsiaras WG, Pezzoli G, Brice A, Smith RJ (Apr 2008). “Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease” (free full text). Am J Hum Genet 82 (4): 822-833. doi:10.1016/j.ajhg.2008.01.015. PMID 18358451.
Higashi S, Iseki E, Minegishi M, Togo T, Kabuta T, Wada K (Oct 2010). “GIGYF2 is present in endosomal compartments in the mammalian brains and enhances IGF-1-induced ERK1/2 activation”. J Neurochem 115 (2): 423-437. doi:10.1111/j.1471-4159.2010.06930.x. PMID 20670374.
Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, Gasser T, Wszolek Z, Muller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, Kruger R (Aug 2005). “Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease” (full text). Hum Mol Genet 14 (15): 2099-2111. doi:10.1093/hmg/ddi215. PMID 15961413.
Paisan-Ruiz C, Bhatia KP, Li A, Hernandez D, Davis M, Wood NW, Hardy J, Houlden H, Singleton A, Schneider SA (Jan 2009). “Characterization of PLA2G6 as a locus for dystonia-parkinsonism”. Ann Neurol 65 (1): 19-23. doi:10.1002/ana.21415. PMID 18570303.
Yoshino H, Tomiyama H, Tachibana N, Ogaki K, Li Y, Funayama M, Hashimoto T, Takashima S, Hattori N (Oct 2010). “Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism”. Neurology 75 (15): 1356-61. doi:10.1212/WNL.0b013e3181f73649. PMID 20938027.
Matsuda N, Sato S, Shiba K, Okatsu K, Saisho K, Gautier CA, Sou YS, Saiki S, Kawajiri S, Sato F, Kimura M, Komatsu M, Hattori N, Tanaka K (Apr 2010). “PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy” (full text). J Cell Biol 189 (2): 211-221. doi:10.1083/jcb.200910140. PMID 20404107.
Narendra, D; Tanaka, A; Suen, DF; Youle, RJ (Dec 2008). “Parkin is recruited selectively to impaired mitochondria and promotes their autophagy” (full text). J Cell Biol 183 (5): 795-803. doi:10.1083/jcb.200809125. PMID 19029340.
Mizuta I, Satake W, Nakabayashi Y, Ito C, Suzuki S, Momose Y, Nagai Y, Oka A, Inoko H, Fukae J, Saito Y, Sawabe M, Murayama S, Yamamoto M, Hattori N, Murata M, Toda T (Apr 2006). “Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease” (full text). Hum Mol Genet 15 (7): 1151-1158. doi:10.1093/hmg/ddl030. PMID 16500997.
Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T (Dec 2009). “Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease”. Nat Genet 41 (12): 1303-1307. doi:10.1038/ng.485. PMID 19915576.
Simon-Sanchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, Berg D, Paisan-Ruiz C, Lichtner P, Scholz SW, Hernandez DG, Kruger R, Federoff M, Klein C, Goate A, Perlmutter J, Bonin M, Nalls MA, Illig T, Gieger C, Houlden H, Steffens M, Okun MS, Racette BA, Cookson MR, Foote KD, Fernandez HH, Traynor BJ, Schreiber S, Arepalli S, Zonozi R, Gwinn K, van der Brug M, Lopez G, Chanock SJ, Schatzkin A, Park Y, Hollenbeck A, Gao J, Huang X, Wood NW, Lorenz D, Deuschl G, Chen H, Riess O, Hardy JA, Singleton AB, Gasser T (Dec 2009). “Genome-wide association study reveals genetic risk underlying Parkinson's disease” (free full text). Nat Genet 41 (12): 1308-1312. doi:10.1038/ng.487. PMID 19915575.
戸田達史「変わりゆくパーキンソン病診療早期診断から進行期患者の治療まで孤発性パーキンソン病の分子病態機序はどこまで解明されたか」『内科』第107巻第5号、南江堂、2011年5月、759-766頁、doi:10.15106/j00974.2011189945、ISSN 00221961。
Aharon-Peretz, J; Rosenbaum, H; Gershoni-Baruch, R (Nov 2004). “Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews” (free full text). N Eng j Med 351 (19): 1972-1977. doi:10.1056/NEJMoa033277. PMID 15525722.
Mitsui J, Mizuta I, Toyoda A, Ashida R, Takahashi Y, Goto J, Fukuda Y, Date H, Iwata A, Yamamoto M, Hattori N, Murata M, Toda T, Tsuji S (May 2009). “Mutations for Gaucher disease confer high susceptibility to Parkinson disease”. Arch Neurol 66 (5): 571-576. doi:10.1001/archneurol.2009.72. PMID 19433656.
Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Durr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, Marder K, Mata IF, Mirelman A, Mitsui J, Mizuta I, Nicoletti G, Oliveira C, Ottman R, Orr-Urtreger A, Pereira LV, Quattrone A, Rogaeva E, Rolfs A, Rosenbaum H, Rozenberg R, Samii A, Samaddar T, Schulte C, Sharma M, Singleton A, Spitz M, Tan EK, Tayebi N, Toda T, Troiano AR, Tsuji S, Wittstock M, Wolfsberg TG, Wu YR, Zabetian CP, Zhao Y, Ziegler SG (Oct 2009). “Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease” (free full text). N Eng J Med 361 (17): 1651-1661. doi:10.1056/NEJMoa0901281. PMID 19846850.

eisai.co.jp

AMPA受容体拮抗剤E2007（一般名：ペランパネル）の開発状況についてパーキンソン病適応の開発中止と神経因性疼痛、てんかん開発への集中展開エーザイ株式会社ニュースリリース（2008年4月11日）2023年6月10日閲覧

fnn.jp

“iPS細胞でパーキンソン病治療京大が世界初の治験”. フジニュースネットワーク. (2018年11月9日). https://www.fnn.jp/posts/00405153CX 2018年11月9日閲覧。

handle.net

hdl.handle.net

大越教夫「パーキンソン病における補完代替医療に関する実施状況」『筑波技術大学テクノレポート』2007年 14巻 p.207-211, hdl:10460/185, 筑波技術大学学術・社会貢献推進委員会

itmedia.co.jp

““STAP騒動”横目に「京大iPS」着々……パーキンソン病治療で臨床研究へ「一歩一歩」”. ITmedia. (2014年4月17日) 2014年5月6日閲覧。

jamas.or.jp

search.jamas.or.jp

河尻澄宏; 服部信孝 (12 2010). “若年性パーキンソン病”. 『綜合臨牀』 59 (12): 2392-2395. ISSN 03711900. (要購読契約)

jmedj.co.jp

“パーキンソン病と漢方”. 2018年10月17日閲覧。

jsdnnm.com

“パーキンソン病とよだれ(2017/07) | JSDNNM｜日本神経筋疾患摂食・嚥下・栄養研究会公式ホームページ”. www.jsdnnm.com. 2018年10月16日閲覧。

juntendo.ac.jp

パーキンソン病や認知症の原因タンパク質が血液検査で検出可能に順天堂大学（2023年5月30日）2023年6月10日閲覧

kahyo.com

林明人「Parkinson病と音楽療法」第67巻第3号、2007年10月。 (要購読契約)

kampo-s.jp

屋嘉比康治「パーキンソン病に伴う消化器症状に対する六君子湯の効果」（PDF）『漢方医学』第42巻第2号、協和企画、2018年、58-61頁、ISSN 02882485、国立国会図書館書誌ID:029035445。 (要登録)

kyoto-np.co.jp

「iPSでパーキンソン病改善サルで１年超有効確認^{[リンク切れ]}」

lillyanswers.jp

m3.com

新薬15製品を収載へミクスOnline 2018年5月18日記事

mayoclinic.org

“Parkinson's disease - Symptoms and causes” (英語). Mayo Clinic. 2024年3月21日閲覧。

mdpi.com

Ergothioneine Prevents Neuronal Cell Death Caused by the Neurotoxin 6-Hydroxydopamine Cells 2024, 13, 230.

medica.co.jp

www2.medica.co.jp

パーキンソン病においてMIBG心筋シンチグラフィはどのように使われますか?

mhlw.go.jp

平成24年度衛生行政報告例の概況特定疾患（難病）関係厚生労働省平成25年10月24日
厚生労働省：平成23年度衛生行政報告の概況7特定疾患 (難病) 関係

mixonline.jp

薬食審・第一部会新薬７製品を審議、全て承認了承糖尿病薬スージャヌ、腰椎椎間板ヘルニア薬ヘルニコアなどミクスOnline 2018年3月2日記事

movementdisorders.org

D, Devos (May 2009). format=full text “Patient profile, indications, efficacy and safety of duodenal levodopa infusion in advanced Parkinson's disease”. Mov Disord 24 (7): 993-1000. doi:10.1002/mds.22450. PMID 19253412.

nanbyou.or.jp

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“パーキンソン病（指定難病６） – 難病情報センター”. www.nanbyou.or.jp. 2024年4月2日閲覧。
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pubmedcentral.nih.gov

Mizuno, Y et al. (2008), “Progress in the pathogenesis and genetics of Parkinson's disease”, Philos Trans R Soc Lond B Biol Sci 363: 2215-27, PMID 18426756 full text
Hampshire, DJ; Roberts, E; Crow, Y; Bond, J; Mubaidin, A; Wriekat, AL; Al-Din, A; Woods, CG (2001), “Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36.”, J Med Genet 38: 680-682, PMID 11584046 full text