Hanna MG - Search Results

1

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Hanna MG, Nelson IP, Rahman S, Lane RJ, Land J, Heales S, Cooper MJ, Schapira AH, Morgan-Hughes JA, Wood NW. Hanna MG, et al. Am J Hum Genet. 1998 Jul;63(1):29-36. doi: 10.1086/301910. Am J Hum Genet. 1998. PMID: 9634511 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

Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.

Hanna MG, Nelson I, Sweeney MG, Cooper JM, Watkins PJ, Morgan-Hughes JA, Harding AE. Hanna MG, et al. Am J Hum Genet. 1995 May;56(5):1026-33. Am J Hum Genet. 1995. PMID: 7726155 Free PMC article.

5

Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A-->G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA.

Hanna MG, Nelson IP, Morgan-Hughes JA, Harding AE. Hanna MG, et al. J Neurol Sci. 1995 Jun;130(2):154-60. doi: 10.1016/0022-510x(95)00022-t. J Neurol Sci. 1995. PMID: 8586979

6

Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion.

Hanna MG, Davis MB, Sweeney MG, Noursadeghi M, Ellis CJ, Elliot P, Wood NW, Marsden CD. Hanna MG, et al. Mov Disord. 1998 Mar;13(2):339-40. doi: 10.1002/mds.870130223. Mov Disord. 1998. PMID: 9539351

7

Depletion of mitochondrial DNA by ddC in untransformed human cell lines.

Nelson I, Hanna MG, Wood NW, Harding AE. Nelson I, et al. Among authors: hanna mg. Somat Cell Mol Genet. 1997 Jul;23(4):287-90. doi: 10.1007/BF02674419. Somat Cell Mol Genet. 1997. PMID: 9542530

8

Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A).

Hanna MG, Stewart J, Schapira AH, Wood NW, Morgan-Hughes JA, Murray NM. Hanna MG, et al. J Neurol Neurosurg Psychiatry. 1998 Aug;65(2):248-50. doi: 10.1136/jnnp.65.2.248. J Neurol Neurosurg Psychiatry. 1998. PMID: 9703181 Free PMC article.

9

Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders.

Hanna MG, Wood NW, Kullmann DM. Hanna MG, et al. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):427-31. doi: 10.1136/jnnp.65.4.427. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771758 Free PMC article. Review. No abstract available.

10

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.

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