Browse by UCL people
Group by: Type | Date
Number of items: 7.
Article
Gardiner, AR;
Jaffer, F;
Dale, RC;
Labrum, R;
Erro, R;
Meyer, E;
Xiromerisiou, G;
... Houlden, H; + view all
(2015)
The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Brain
, 138
(Pt 12)
pp. 3567-3580.
10.1093/brain/awv310.
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Jaffer, F;
Avbersek, A;
Vavassori, R;
Fons, C;
Campistol, J;
Stagnaro, M;
De Grandis, E;
... Sisodiya, SM; + view all
(2015)
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Brain
, 138
(10)
pp. 2859-2874.
10.1093/brain/awv243.
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Jaffer, F;
Fawcett, K;
Sims, D;
Heger, A;
Houlden, H;
Hanna, MG;
Kingston, H;
(2017)
Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation.
Neurology Genetics
, 3
(2)
, Article e145. 10.1212/NXG.0000000000000145.
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Matthews, E;
Neuwirth, C;
Jaffer, F;
Scalco, RS;
Fialho, D;
Parton, M;
Raja Rayan, D;
... Hanna, MG; + view all
(2018)
Atypical periodic paralysis and myalgia: A novel RYR1 phenotype.
Neurology
, 90
(5)
e412-e418.
10.1212/WNL.0000000000004894.
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Scalco, RS;
Quinlivan, RM;
Nastasi, L;
Jaffer, F;
Hanna, MG;
(2020)
Improving specialised care for neuromuscular patients reduces the frequency of preventable emergency hospital admissions.
Neuromuscular Disorders
, 30
(2)
pp. 173-179.
10.1016/j.nmd.2019.11.013.
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Stern, WM;
Desikan, M;
Hoad, D;
Jaffer, F;
Strigaro, G;
Sander, JW;
Rothwell, JC;
(2016)
Spontaneously Fluctuating Motor Cortex Excitability in Alternating Hemiplegia of Childhood: A Transcranial Magnetic Stimulation Study.
PLoS One
, 11
(3)
, Article e0151667. 10.1371/journal.pone.0151667.
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Report
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Korkodilos, M;
Hajioff, S;
Gardner, C;
Overett, S;
Ibrahim, S;
Jaffer, F;
Hanna, MG;
(2012)
Audit of unplanned admissions in neuromuscular patients: a collaborative audit.
Audit, Information and Analysis Unit / London Specialised Commissioning Group / MRC Centre for Neuromuscular Diseases: United Kingdom.
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