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

Year Number of Results
1991 1
1992 7
1993 4
1994 4
1995 8
1996 1
1997 3
1998 3
1999 3
2000 1
2002 3
2003 4
2004 1
2005 3
2007 3
2008 6
2009 3
2010 2
2011 5
2012 8
2013 9
2014 10
2015 10
2016 6
2017 1
2018 4
2019 1
2022 1
2025 0

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103 results

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Page 1
Extra-ocular muscle MRI in genetically-defined mitochondrial disease.
Pitceathly RD, Morrow JM, Sinclair CD, Woodward C, Sweeney MG, Rahman S, Plant GT, Ali N, Bremner F, Davagnanam I, Yousry TA, Hanna MG, Thornton JS. Pitceathly RD, et al. Among authors: sweeney mg. Eur Radiol. 2016 Jan;26(1):130-7. doi: 10.1007/s00330-015-3801-5. Epub 2015 May 21. Eur Radiol. 2016. PMID: 25994195 Free PMC article.
Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease.
Broomfield A, Sweeney MG, Woodward CE, Fratter C, Morris AM, Leonard JV, Abulhoul L, Grunewald S, Clayton PT, Hanna MG, Poulton J, Rahman S. Broomfield A, et al. Among authors: sweeney mg. J Inherit Metab Dis. 2015 May;38(3):445-57. doi: 10.1007/s10545-014-9778-4. Epub 2014 Oct 29. J Inherit Metab Dis. 2015. PMID: 25352051 Free PMC article.
The phenotypic manifestations of chromosome 17p11.2 duplication.
Thomas PK, Marques W Jr, Davis MB, Sweeney MG, King RH, Bradley JL, Muddle JR, Tyson J, Malcolm S, Harding AE. Thomas PK, et al. Among authors: sweeney mg. Brain. 1997 Mar;120 ( Pt 3):465-78. doi: 10.1093/brain/120.3.465. Brain. 1997. PMID: 9126058
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.
Hensman Moss DJ, Poulter M, Beck J, Hehir J, Polke JM, Campbell T, Adamson G, Mudanohwo E, McColgan P, Haworth A, Wild EJ, Sweeney MG, Houlden H, Mead S, Tabrizi SJ. Hensman Moss DJ, et al. Among authors: sweeney mg. Neurology. 2014 Jan 28;82(4):292-9. doi: 10.1212/WNL.0000000000000061. Epub 2013 Dec 20. Neurology. 2014. PMID: 24363131 Free PMC article.
PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutations.
Yao Z, Jones AW, Fassone E, Sweeney MG, Lebiedzinska M, Suski JM, Wieckowski MR, Tajeddine N, Hargreaves IP, Yasukawa T, Tufo G, Brenner C, Kroemer G, Rahman S, Szabadkai G. Yao Z, et al. Among authors: sweeney mg. Oncogene. 2013 May 16;32(20):2592-600. doi: 10.1038/onc.2012.259. Epub 2012 Jul 9. Oncogene. 2013. PMID: 22777349
Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.
Bugiardini E, Poole OV, Manole A, Pittman AM, Horga A, Hargreaves I, Woodward CE, Sweeney MG, Holton JL, Taanman JW, Plant GT, Poulton J, Zeviani M, Ghezzi D, Taylor J, Smith C, Fratter C, Kanikannan MA, Paramasivam A, Thangaraj K, Spinazzola A, Holt IJ, Houlden H, Hanna MG, Pitceathly RDS. Bugiardini E, et al. Among authors: sweeney mg. Neurol Genet. 2017 May 2;3(3):e149. doi: 10.1212/NXG.0000000000000149. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28508084 Free PMC article.
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: sweeney mg. Biochim Biophys Acta. 1995 May 24;1271(1):135-40. doi: 10.1016/0925-4439(95)00020-5. Biochim Biophys Acta. 1995. PMID: 7599199 Free article.
103 results