Hanna Michael
Hanna Michael
UCL Institute of Neurology
Verified email at ucl.ac.uk - Homepage
Title
Cited by
Cited by
Year
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
AL Andreu, MG Hanna, H Reichmann, C Bruno, AS Penn, K Tanji, ...
New England Journal of Medicine 341 (14), 1037-1044, 1999
4381999
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel
A Jouvenceau, LH Eunson, A Spauschus, V Ramesh, SM Zuberi, ...
The Lancet 358 (9284), 801-807, 2001
4312001
Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene
R Horvath, G Hudson, G Ferrari, N Fütterer, S Ahola, E Lamantea, ...
Brain 129 (7), 1674-1684, 2006
4072006
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
SM Zuberi, LH Eunson, A Spauschus, R De Silva, J Tolmie, NW Wood, ...
Brain 122 (5), 817-825, 1999
3891999
The primary periodic paralyses: diagnosis, pathogenesis and treatment
SL Venance, SC Cannon, D Fialho, B Fontaine, MG Hanna, LJ Ptacek, ...
Brain 129 (1), 8-17, 2006
3232006
Primary episodic ataxias: diagnosis, pathogenesis and treatment
JC Jen, TD Graves, EJ Hess, MG Hanna, RC Griggs, RW Baloh, ...
Brain 130 (10), 2484-2493, 2007
3072007
International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in …
DA Isenberg, E Allen, V Farewell, MR Ehrenstein, MG Hanna, ...
Rheumatology 43 (1), 49-54, 2004
3012004
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability
LH Eunson, R Rea, SM Zuberi, S Youroukos, CP Panayiotopoulos, ...
Annals of Neurology: Official Journal of the American Neurological …, 2000
2862000
Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions
HY Lee, Y Huang, N Bruneau, P Roll, EDO Roberson, M Hermann, ...
Cell reports 1 (1), 2-12, 2012
2512012
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia
P Imbrici, SL Jaffe, LH Eunson, NP Davies, C Herd, R Robertson, ...
Brain 127 (12), 2682-2692, 2004
2362004
Apixaban in comparison with warfarin in patients with atrial fibrillation and valvular heart disease: findings from the apixaban for reduction in stroke and other …
A Avezum, RD Lopes, PJ Schulte, F Lanas, BJ Gersh, M Hanna, P Pais, ...
Circulation 132 (8), 624-632, 2015
2232015
MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study
JM Morrow, CDJ Sinclair, A Fischmann, PM Machado, MM Reilly, ...
The Lancet Neurology 15 (1), 65-77, 2016
2162016
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
GL Cavalleri, ME Weale, KV Shianna, R Singh, JM Lynch, B Grinton, ...
The Lancet Neurology 6 (11), 970-980, 2007
2152007
The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment
E Matthews, D Fialho, SV Tan, SL Venance, SC Cannon, D Sternberg, ...
Brain 133 (1), 9-22, 2010
2052010
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m. 3243A> G mutation—implications for diagnosis and management
V Nesbitt, RDS Pitceathly, DM Turnbull, RW Taylor, MG Sweeney, ...
Journal of Neurology, Neurosurgery & Psychiatry 84 (8), 936-938, 2013
1922013
The mitochondrial DNA transfer RNA Leu(UUR) A→G(3243) mutation: A clinical and genetic study
SR Hammans, MG Sweeney, MG Hanna, M Brockington, ...
Brain 118 (3), 721-734, 1995
1891995
Apixaban vs. warfarin with concomitant aspirin in patients with atrial fibrillation: insights from the ARISTOTLE trial
JH Alexander, RD Lopes, L Thomas, M Alings, D Atar, P Aylward, S Goto, ...
European heart journal 35 (4), 224-232, 2014
1862014
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
E Matthews, R Labrum, MG Sweeney, R Sud, A Haworth, PF Chinnery, ...
Neurology 72 (18), 1544-1547, 2009
1862009
Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history
RT Murphy, J Mogensen, K McGarry, A Bahl, A Evans, E Osman, P Syrris, ...
Journal of the American College of Cardiology 45 (6), 922-930, 2005
1722005
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine
AR Gardiner, KP Bhatia, M Stamelou, RC Dale, MA Kurian, SA Schneider, ...
Neurology 79 (21), 2115-2121, 2012
1662012
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