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Items: 1 to 20 of 102

1.

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.

Ogaki K, Koga S, Heckman MG, Fiesel FC, Ando M, Labbé C, Lorenzo-Betancor O, Moussaud-Lamodière EL, Soto-Ortolaza AI, Walton RL, Strongosky AJ, Uitti RJ, McCarthy A, Lynch T, Siuda J, Opala G, Rudzinska M, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Puschmann A, Nishioka K, Funayama M, Hattori N, Parisi JE, Petersen RC, Graff-Radford NR, Boeve BF, Springer W, Wszolek ZK, Dickson DW, Ross OA.

Neurology. 2015 Dec 8;85(23):2016-25. doi: 10.1212/WNL.0000000000002170. Epub 2015 Nov 11.

2.

Rare genetic variants support mitochondrial dysfunction in Lewy body disorders.

Wider C, Mouradian MM.

Neurology. 2015 Dec 8;85(23):2002-3. doi: 10.1212/WNL.0000000000002182. Epub 2015 Nov 11. No abstract available.

PMID:
26561295
3.

Genetic analysis of CHCHD2 in a southern Spanish population.

Tejera-Parrado C, Jesús S, Huertas-Fernández I, Bernal-Bernal I, Bonilla-Toribio M, Córdoba-Tevar I, Abreu-Rodríguez I, Carrillo F, Bernal-Escudero M, Vargas-González L, Carballo M, Gómez-Garre P, Mir P.

Neurobiol Aging. 2017 Feb;50:169.e1-169.e2. doi: 10.1016/j.neurobiolaging.2016.10.019. Epub 2016 Oct 21.

PMID:
27839904
4.

Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson's disease.

Rubino E, Brusa L, Zhang M, Boschi S, Govone F, Vacca A, Gai A, Pinessi L, Lopiano L, Rogaeva E, Rainero I.

Neurobiol Aging. 2017 May;53:193.e7-193.e8. doi: 10.1016/j.neurobiolaging.2016.12.027. Epub 2017 Jan 5.

PMID:
28108040
5.

Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor.

Wu H, Lu X, Cen Z, Xie F, Zheng X, Chen Y, Luo W.

Neurosci Lett. 2016 Nov 10;634:104-106. doi: 10.1016/j.neulet.2016.10.005. Epub 2016 Oct 4.

PMID:
27717833
6.

Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease.

Li NN, Wang L, Tan EK, Cheng L, Sun XY, Lu ZJ, Li JY, Zhang JH, Peng R.

Am J Med Genet B Neuropsychiatr Genet. 2016 Dec;171(8):1148-1152. doi: 10.1002/ajmg.b.32498. Epub 2016 Sep 14.

PMID:
27626775
7.

A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease.

Zheng K, Heydari B, Simon DK.

Arch Neurol. 2003 May;60(5):722-5.

PMID:
12756136
8.

Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease.

Wu H, Lu X, Xie F, Cen Z, Zheng X, Luo W.

Neurosci Lett. 2016 Aug 26;629:116-118. doi: 10.1016/j.neulet.2016.06.054. Epub 2016 Jun 25.

PMID:
27353515
9.

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.

Labbé C, Ogaki K, Lorenzo-Betancor O, Soto-Ortolaza AI, Walton RL, Rayaprolu S, Fujioka S, Murray ME, Heckman MG, Puschmann A, McCarthy A, Lynch T, Siuda J, Opala G, Rudzinska M, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Sanotsky Y, Rektorová I, McLean PJ, Rademakers R, Ertekin-Taner N, Hassan A, Ahlskog JE, Boeve BF, Petersen RC, Maraganore DM, Adler CH, Ferman TJ, Parisi JE, Graff-Radford NR, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA.

Neurology. 2015 Nov 10;85(19):1680-6. doi: 10.1212/WNL.0000000000001946. Epub 2015 Sep 2. Erratum in: Neurology. 2015 Nov 10;85(19):1728.

10.

Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literature.

Yang X, Zhao Q, An R, Zheng J, Tian S, Chen Y, Xu Y.

Parkinsonism Relat Disord. 2016 Aug;29:42-6. doi: 10.1016/j.parkreldis.2016.05.032. Epub 2016 May 30.

PMID:
27269965
11.

Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population.

Fan TS, Lin HI, Lin CH, Wu RM.

Neurobiol Aging. 2016 Feb;38:218.e1-218.e2. doi: 10.1016/j.neurobiolaging.2015.11.020. Epub 2015 Dec 8.

PMID:
26725463
12.

Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.

Zhang M, Xi Z, Fang S, Ghani M, Sato C, Moreno D, Liang Y, Lang AE, Rogaeva E.

Neurobiol Aging. 2016 Feb;38:217.e7-217.e8. doi: 10.1016/j.neurobiolaging.2015.10.038. Epub 2015 Nov 6.

PMID:
26639156
13.

Mutation analysis of CHCHD2 gene in Chinese Han familial essential tremor patients and familial Parkinson's disease patients.

Gao C, Chen YM, Sun Q, He YC, Huang P, Wang T, Li DH, Liang L, Liu J, Xiao Q, Chen SD.

Neurobiol Aging. 2017 Jan;49:218.e9-218.e11. doi: 10.1016/j.neurobiolaging.2016.10.001. Epub 2016 Oct 11.

PMID:
27814991
14.

CHCHD2 gene mutations in familial and sporadic Parkinson's disease.

Shi CH, Mao CY, Zhang SY, Yang J, Song B, Wu P, Zuo CT, Liu YT, Ji Y, Yang ZH, Wu J, Zhuang ZP, Xu YM.

Neurobiol Aging. 2016 Feb;38:217.e9-217.e13. doi: 10.1016/j.neurobiolaging.2015.10.040. Epub 2015 Nov 6.

PMID:
26705026
15.

Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis.

Yang X, An R, Zhao Q, Zheng J, Tian S, Chen Y, Xu Y.

J Neurol Sci. 2016 Sep 15;368:389-91. doi: 10.1016/j.jns.2016.07.063. Epub 2016 Jul 28.

PMID:
27538669
16.

Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease.

Liu Z, Guo J, Li K, Qin L, Kang J, Shu L, Zhang Y, Wei Y, Yang N, Luo Y, Sun Q, Xu Q, Yan X, Tang B.

Neurobiol Aging. 2015 Nov;36(11):3117.e7-3117.e8. doi: 10.1016/j.neurobiolaging.2015.08.010. Epub 2015 Aug 15.

PMID:
26343503
17.

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study.

Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Li Y, Ogaki K, Ando M, Yoshino H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake W, Mogushi K, Sasaki R, Kokubo Y, Kuzuhara S, Toda T, Mizuno Y, Uchiyama Y, Ohno K, Hattori N.

Lancet Neurol. 2015 Mar;14(3):274-82. doi: 10.1016/S1474-4422(14)70266-2. Epub 2015 Feb 4.

PMID:
25662902
18.

[Diagnostic value of cardiac 123I-metaiodobenzylguanidine (123I-MIBG) scintigraphy in Lewy body disorders].

Escamilla-Sevilla F, Pérez-Navarro MJ, Muñoz-Pasadas M, Ortega-Léon T, Gallego-Peinado M, Cabello-García D, Gómez Río M, Ortega-Moreno A, Carnero-Pardo C, Rebollo-Aguirre AC, Mínguez-Castellanos A.

Neurologia. 2009 Apr;24(3):170-6. Spanish.

PMID:
19418293
19.

Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria.

Gagliardi M, Iannello G, Colica C, Annesi G, Quattrone A.

Neurobiol Aging. 2017 Feb;50:169.e5-169.e6. doi: 10.1016/j.neurobiolaging.2016.10.022. Epub 2016 Oct 21.

PMID:
27839905
20.

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

Lorenzo-Betancor O, Ogaki K, Soto-Ortolaza AI, Labbe C, Walton RL, Strongosky AJ, van Gerpen JA, Uitti RJ, McLean PJ, Springer W, Siuda J, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, McCarthy A, Lynch T, Puschmann A, Rektorova I, Sanotsky Y, Vilariño-Güell C, Farrer MJ, Ferman TJ, Boeve BF, Petersen RC, Parisi JE, Graff-Radford NR, Dickson DW, Wszolek ZK, Ross OA.

Eur J Neurol. 2015 Sep;22(9):1323-5. doi: 10.1111/ene.12770.

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