S. Omer

发表

Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1

Len A. Pennacchio, Ralf Krahe, Silvana Franceschetti, 1997, Nature Genetics.

A new mitochondrial transfer RNAPro gene mutation associated with myoclonic epilepsy with ragged-red fibers and other neurological features.

Robert W. Taylor, D. Turnbull, P. Rich, 2009, Archives of neurology.

Determination of hemoglobin level, mean cell volume and red cell distribution width among patients with renal failure in Khartoum state

S. Omer, Salam, A. Eltom, 2022 .

Early-onset Lafora body disease.

S. Scherer, C. Ackerley, Peixiang Wang, 2012, Brain : a journal of neurology.

Progressive myoclonus epilepsy with polyglucosans (Lafora disease)

S. Scherer, B. Minassian, M. Ahmed, 2004, Neurology.

Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis.

M. Rossor, J. Schott, J. Palace, 2004, Brain : a journal of neurology.

Transient facial weakness whilst on a flight

U. Vivekananda, S. Omer, 2017, Journal of the Neurological Sciences.

The imploding antrum syndrome: an unusual cause of double vision

P. Rich, S. Omer, A. Almemar, 2010, Practical Neurology.

Upbeat nystagmus in anti-Ma2 encephalitis

S. Omer, C. Griffin, P. Johns, 2013, Practical Neurology.

Prominent cognitive decline and behavioural disturbance in late-onset Alexander disease

C. Lambert, S. Omer, M. McEntagart, 2015, Journal of the Neurological Sciences.