Hanna MG - Search Results

1

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.

Cavalleri GL, Weale ME, Shianna KV, Singh R, Lynch JM, Grinton B, Szoeke C, Murphy K, Kinirons P, O'Rourke D, Ge D, Depondt C, Claeys KG, Pandolfo M, Gumbs C, Walley N, McNamara J, Mulley JC, Linney KN, Sheffield LJ, Radtke RA, Tate SK, Chissoe SL, Gibson RA, Hosford D, Stanton A, Graves TD, Hanna MG, Eriksson K, Kantanen AM, Kalviainen R, O'Brien TJ, Sander JW, Duncan JS, Scheffer IE, Berkovic SF, Wood NW, Doherty CP, Delanty N, Sisodiya SM, Goldstein DB. Cavalleri GL, et al. Among authors: hanna mg. Lancet Neurol. 2007 Nov;6(11):970-80. doi: 10.1016/S1474-4422(07)70247-8. Lancet Neurol. 2007. PMID: 17913586

2

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

3

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.

4

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.

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

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

Zuberi SM, Eunson LH, Spauschus A, De Silva R, Tolmie J, Wood NW, McWilliam RC, Stephenson JB, Kullmann DM, Hanna MG. Zuberi SM, et al. Among authors: hanna mg. Brain. 1999 May;122 ( Pt 5):817-25. doi: 10.1093/brain/122.5.817. Brain. 1999. PMID: 10355668

7

Phenotypic variation of a new P0 mutation in genetically identical twins.

Marques W Jr, Hanna MG, Marques SR, Sweeney MG, Thomas PK, Wood NW. Marques W Jr, et al. Among authors: hanna mg. J Neurol. 1999 Jul;246(7):596-9. doi: 10.1007/s004150050410. J Neurol. 1999. PMID: 10463363

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

A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.

Münchau A, Valente EM, Shahidi GA, Eunson LH, Hanna MG, Quinn NP, Schapira AH, Wood NW, Bhatia KP. Münchau A, et al. Among authors: hanna mg. J Neurol Neurosurg Psychiatry. 2000 May;68(5):609-14. doi: 10.1136/jnnp.68.5.609. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766892 Free PMC article.

10

Intrafamilial phenotypic variability in Friedreich ataxia associated with a G130V mutation in the FRDA gene.

McCabe DJ, Wood NW, Ryan F, Hanna MG, Connolly S, Moore DP, Redmond J, Barton DE, Murphy RP. McCabe DJ, et al. Among authors: hanna mg. Arch Neurol. 2002 Feb;59(2):296-300. doi: 10.1001/archneur.59.2.296. Arch Neurol. 2002. PMID: 11843702

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