These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
12. Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis. Bannwarth S; Ait-El-Mkadem S; Chaussenot A; Genin EC; Lacas-Gervais S; Fragaki K; Berg-Alonso L; Kageyama Y; Serre V; Moore D; Verschueren A; Rouzier C; Le Ber I; Augé G; Cochaud C; Lespinasse F; N'Guyen K; de Septenville A; Brice A; Yu-Wai-Man P; Sesaki H; Pouget J; Paquis-Flucklinger V Brain; 2014 Dec; 137(Pt 12):e312. PubMed ID: 25261971 [No Abstract] [Full Text] [Related]
13. A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. Kurzwelly D; Krüger S; Biskup S; Heneka MT Brain; 2015 Sep; 138(Pt 9):e376. PubMed ID: 25681414 [No Abstract] [Full Text] [Related]
14. Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. Bannwarth S; Ait-El-Mkadem S; Chaussenot A; Genin EC; Lacas-Gervais S; Fragaki K; Berg-Alonso L; Kageyama Y; Serre V; Moore D; Verschueren A; Rouzier C; Le Ber I; Augé G; Cochaud C; Lespinasse F; N'Guyen K; de Septenville A; Brice A; Yu-Wai-Man P; Sesaki H; Pouget J; Paquis-Flucklinger V Brain; 2014 Dec; 137(Pt 12):e310. PubMed ID: 25113788 [No Abstract] [Full Text] [Related]
15. Mutation analysis of CHCHD10 in different neurodegenerative diseases. Zhang M; Xi Z; Zinman L; Bruni AC; Maletta RG; Curcio SA; Rainero I; Rubino E; Pinessi L; Nacmias B; Sorbi S; Galimberti D; Lang AE; Fox S; Surace EI; Ghani M; Guo J; Sato C; Moreno D; Liang Y; Keith J; Traynor BJ; St George-Hyslop P; Rogaeva E Brain; 2015 Sep; 138(Pt 9):e380. PubMed ID: 25833818 [No Abstract] [Full Text] [Related]
16. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement. Bannwarth S; Ait-El-Mkadem S; Chaussenot A; Genin EC; Lacas-Gervais S; Fragaki K; Berg-Alonso L; Kageyama Y; Serre V; Moore DG; Verschueren A; Rouzier C; Le Ber I; Augé G; Cochaud C; Lespinasse F; N'Guyen K; de Septenville A; Brice A; Yu-Wai-Man P; Sesaki H; Pouget J; Paquis-Flucklinger V Brain; 2014 Aug; 137(Pt 8):2329-45. PubMed ID: 24934289 [TBL] [Abstract][Full Text] [Related]
17. Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. Bannwarth S; Ait-El-Mkadem S; Chaussenot A; Genin EC; Lacas-Gervais S; Fragaki K; Berg-Alonso L; Kageyama Y; Serre V; Moore D; Verschueren A; Rouzier C; Le Ber I; Augé G; Cochaud C; Lespinasse F; N'Guyen K; de Septenville A; Brice A; Yu-Wai-Man P; Sesaki H; Pouget J; Paquis-Flucklinger V Brain; 2015 Sep; 138(Pt 9):e377. PubMed ID: 25681413 [No Abstract] [Full Text] [Related]
18. The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients. Wong CH; Topp S; Gkazi AS; Troakes C; Miller JW; de Majo M; Kirby J; Shaw PJ; Morrison KE; de Belleroche J; Vance CA; Al-Chalabi A; Al-Sarraj S; Shaw CE; Smith BN Neurobiol Aging; 2015 Oct; 36(10):2908.e17-8. PubMed ID: 26344877 [TBL] [Abstract][Full Text] [Related]
19. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. Chaussenot A; Le Ber I; Ait-El-Mkadem S; Camuzat A; de Septenville A; Bannwarth S; Genin EC; Serre V; Augé G; ; Brice A; Pouget J; Paquis-Flucklinger V Neurobiol Aging; 2014 Dec; 35(12):2884.e1-2884.e4. PubMed ID: 25155093 [TBL] [Abstract][Full Text] [Related]
20. Twin CHCH Proteins, CHCHD2, and CHCHD10: Key Molecules of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Frontotemporal Dementia. Imai Y; Meng H; Shiba-Fukushima K; Hattori N Int J Mol Sci; 2019 Feb; 20(4):. PubMed ID: 30791515 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]