Hanna MG - Search Results

1

COVID-19-Related Outcomes in Primary Mitochondrial Diseases: An International Study.

Pizzamiglio C, Machado PM, Thomas RH, Gorman GS, McFarland R, Hanna MG, Pitceathly RDS; MitoCOVID-19 Study Group. Pizzamiglio C, et al. Among authors: hanna mg. Neurology. 2022 Apr 5;98(14):576-582. doi: 10.1212/WNL.0000000000200240. Epub 2022 Feb 21. Neurology. 2022. PMID: 35190464 Free PMC article.

2

The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.

Hammans SR, Sweeney MG, Hanna MG, Brockington M, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Among authors: hanna mg. Brain. 1995 Jun;118 ( Pt 3):721-34. doi: 10.1093/brain/118.3.721. Brain. 1995. PMID: 7600089

3

A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study.

Nelson I, Hanna MG, Alsanjari N, Scaravilli F, Morgan-Hughes JA, Harding AE. Nelson I, et al. Among authors: hanna mg. Ann Neurol. 1995 Mar;37(3):400-3. doi: 10.1002/ana.410370317. Ann Neurol. 1995. PMID: 7695240

4

Movement disorders and mitochondrial dysfunction.

Hanna MG, Bhatia KP. Hanna MG, et al. Curr Opin Neurol. 1997 Aug;10(4):351-6. doi: 10.1097/00019052-199708000-00012. Curr Opin Neurol. 1997. PMID: 9266161 Review.

5

A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intolerance.

Pulkes T, Siddiqui A, Morgan-Hughes JA, Hanna MG. Pulkes T, et al. Among authors: hanna mg. Neurology. 2000 Oct 24;55(8):1210-2. doi: 10.1212/wnl.55.8.1210. Neurology. 2000. PMID: 11071502

6

Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance.

Pulkes T, Liolitsa D, Wills AJ, Hargreaves I, Heales S, Hanna MG. Pulkes T, et al. Among authors: hanna mg. Neurology. 2005 Mar 22;64(6):1091-2. doi: 10.1212/01.WNL.0000154471.33156.55. Neurology. 2005. PMID: 15781840 No abstract available.

7

POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.

Hudson G, Deschauer M, Taylor RW, Hanna MG, Fialho D, Schaefer AM, He LP, Blakely E, Turnbull DM, Chinnery PF. Hudson G, et al. Among authors: hanna mg. Neurology. 2006 May 9;66(9):1439-41. doi: 10.1212/01.wnl.0000210486.32196.24. Neurology. 2006. PMID: 16682683

8

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.

Matthews E, Labrum R, Sweeney MG, Sud R, Haworth A, Chinnery PF, Meola G, Schorge S, Kullmann DM, Davis MB, Hanna MG. Matthews E, et al. Among authors: hanna mg. Neurology. 2009 May 5;72(18):1544-7. doi: 10.1212/01.wnl.0000342387.65477.46. Epub 2008 Dec 31. Neurology. 2009. PMID: 19118277 Free PMC article.

9

Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children.

Stewart JD, Tennant S, Powell H, Pyle A, Blakely EL, He L, Hudson G, Roberts M, du Plessis D, Gow D, Mewasingh LD, Hanna MG, Omer S, Morris AA, Roxburgh R, Livingston JH, McFarland R, Turnbull DM, Chinnery PF, Taylor RW. Stewart JD, et al. Among authors: hanna mg. J Med Genet. 2009 Mar;46(3):209-14. doi: 10.1136/jmg.2008.058180. J Med Genet. 2009. PMID: 19251978

10

Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases.

Rahman S, Hanna MG. Rahman S, et al. Among authors: hanna mg. J Neurol Neurosurg Psychiatry. 2009 Sep;80(9):943-53. doi: 10.1136/jnnp.2008.158279. J Neurol Neurosurg Psychiatry. 2009. PMID: 19684231 Free article. Review.

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