Hanna MG - Search Results

1

A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1.

Raja Rayan DL, Haworth A, Sud R, Matthews E, Fialho D, Burge J, Portaro S, Schorge S, Tuin K, Lunt P, McEntagart M, Toscano A, Davis MB, Hanna MG. Raja Rayan DL, et al. Among authors: hanna mg. Neurology. 2012 Jun 12;78(24):1953-8. doi: 10.1212/WNL.0b013e318259e19c. Epub 2012 May 30. Neurology. 2012. PMID: 22649220 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

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

4

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.

5

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

6

Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenita.

Davies NP, Eunson LH, Gregory RP, Mills KR, Morrison PJ, Hanna MG. Davies NP, et al. Among authors: hanna mg. J Neurol Neurosurg Psychiatry. 2000 Apr;68(4):504-7. doi: 10.1136/jnnp.68.4.504. J Neurol Neurosurg Psychiatry. 2000. PMID: 10727489 Free PMC article.

7

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.

Eunson LH, Rea R, Zuberi SM, Youroukos S, Panayiotopoulos CP, Liguori R, Avoni P, McWilliam RC, Stephenson JB, Hanna MG, Kullmann DM, Spauschus A. Eunson LH, et al. Among authors: hanna mg. Ann Neurol. 2000 Oct;48(4):647-56. Ann Neurol. 2000. PMID: 11026449

8

Sodium channel gene mutations in hypokalemic periodic paralysis: an uncommon cause in the UK.

Davies NP, Eunson LH, Samuel M, Hanna MG. Davies NP, et al. Among authors: hanna mg. Neurology. 2001 Oct 9;57(7):1323-5. doi: 10.1212/wnl.57.7.1323. Neurology. 2001. PMID: 11591859

9

Neurological disorders caused by inherited ion-channel mutations.

Kullmann DM, Hanna MG. Kullmann DM, et al. Among authors: hanna mg. Lancet Neurol. 2002 Jul;1(3):157-66. doi: 10.1016/s1474-4422(02)00071-6. Lancet Neurol. 2002. PMID: 12849484 Review.

10

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.

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