Hanna MG - Search Results

1

Applying genomic and transcriptomic advances to mitochondrial medicine.

Macken WL, Vandrovcova J, Hanna MG, Pitceathly RDS. Macken WL, et al. Among authors: hanna mg. Nat Rev Neurol. 2021 Apr;17(4):215-230. doi: 10.1038/s41582-021-00455-2. Epub 2021 Feb 23. Nat Rev Neurol. 2021. PMID: 33623159 Review.

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

MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity.

Hanna MG, Nelson IP, Morgan-Hughes JA, Wood NW. Hanna MG, et al. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):512-7. doi: 10.1136/jnnp.65.4.512. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771776 Free PMC article.

6

Mitochondrial encephalomyopathies: the enigma of genotype versus phenotype.

Morgan-Hughes JA, Hanna MG. Morgan-Hughes JA, et al. Among authors: hanna mg. Biochim Biophys Acta. 1999 Feb 9;1410(2):125-45. doi: 10.1016/s0005-2728(98)00162-5. Biochim Biophys Acta. 1999. PMID: 10076022 Free article. Review.

7

Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases.

Hanna MG, Nelson IP. Hanna MG, et al. Cell Mol Life Sci. 1999 May;55(5):691-706. doi: 10.1007/s000180050327. Cell Mol Life Sci. 1999. PMID: 10379358 Free PMC article. Review.

8

The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS.

Pulkes T, Eunson L, Patterson V, Siddiqui A, Wood NW, Nelson IP, Morgan-Hughes JA, Hanna MG. Pulkes T, et al. Among authors: hanna mg. Ann Neurol. 1999 Dec;46(6):916-9. doi: 10.1002/1531-8249(199912)46:6<916::aid-ana16>3.0.co;2-r. Ann Neurol. 1999. PMID: 10589546

9

Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms.

Rahman S, Lake BD, Taanman JW, Hanna MG, Cooper JM, Schapira AH, Leonard JV. Rahman S, et al. Among authors: hanna mg. Brain. 2000 Mar;123 Pt 3:591-600. doi: 10.1093/brain/123.3.591. Brain. 2000. PMID: 10686181

10

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

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