Browse by UCL people
Group by: Type | Date
Number of items: 6.
Article
Horga, A;
Raja Rayan, DL;
Matthews, E;
Sud, R;
Fialho, D;
Durran, SC;
Burge, JA;
... Hanna, MG; + view all
(2013)
Prevalence study of genetically defined skeletal muscle channelopathies in England.
Neurology
, 80
(16)
1472 - 1475.
10.1212/WNL.0b013e31828cf8d0.
|
Keddie, S;
Pakpoor, J;
Mousele, C;
Pipis, M;
Machado, PM;
Foster, M;
Record, CJ;
... Lunn, MP; + view all
(2021)
Epidemiological and cohort study finds no association between COVID-19 and Guillain-Barré syndrome.
Brain
, 144
(2)
pp. 682-693.
10.1093/brain/awaa433.
|
Morrow, JM;
Matthews, E;
Raja Rayan, DL;
Fischmann, A;
Sinclair, CD;
Reilly, MM;
Thornton, JS;
... Yousry, TA; + view all
(2013)
Muscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotonias.
Neuromuscular Disorders
, 23
(8)
pp. 637-646.
10.1016/j.nmd.2013.05.001.
|
Suetterlin, K;
Matthews, E;
Sud, R;
McCall, S;
Fialho, D;
Burge, J;
Jayaseelan, D;
... Männikkö, R; + view all
(2021)
Translating genetic and functional data into clinical practice: a series of 223 families with myotonia.
Brain
10.1093/brain/awab344.
(In press).
|
Tan, SV;
Z'graggen, WJ;
Boërio, D;
Rayan, DR;
Norwood, F;
Ruddy, D;
Howard, R;
... Bostock, H; + view all
(2014)
Chloride channels in myotonia congenita assessed by velocity recovery cycles.
Muscle & Nerve
, 49
(6)
pp. 845-857.
10.1002/mus.24069.
|
Thesis
Raja Rayan, DL;
(2016)
A clinical and genetic study of the skeletal muscle channelopathies.
Doctoral thesis , UCL (University College London).
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