Hanna MG - Search Results

1

New calcium channel mutations predict aberrant RNA splicing in episodic ataxia.

Eunson LH, Graves TD, Hanna MG. Eunson LH, et al. Among authors: hanna mg. Neurology. 2005 Jul 26;65(2):308-10. doi: 10.1212/01.wnl.0000169020.82223.dd. Neurology. 2005. PMID: 16043807

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

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.

5

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

6

Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy.

Spauschus A, Eunson L, Hanna MG, Kullmann DM. Spauschus A, et al. Among authors: hanna mg. Ann N Y Acad Sci. 1999 Apr 30;868:442-6. doi: 10.1111/j.1749-6632.1999.tb11310.x. Ann N Y Acad Sci. 1999. PMID: 10414318 No abstract available.

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

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.

10

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.

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