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Salah Omer

Potassium channel antibody‐associated encephalopathy: a potentially immunotherapy‐responsive form of limbic encephalitis
2004 · Angela Vincent, Camilla Buckley, et al. · Brain · 1,038
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Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1
1997 · Kimmo Virtaneva, Elena D'Amato, et al. · Nature Genetics · 191
The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO
2010 · C. Fratter, G.S. Gorman, et al. · Neurology · 95
Early-onset Lafora body disease
2012 · Julie Turnbull, Jean-Marie Girard, et al. · Brain · 90
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Progressive myoclonus epilepsy with polyglucosans (Lafora disease)
2004 · E. M. Chan, S. Omer, et al. · Neurology · 90
A New Mitochondrial Transfer RNAPro Gene Mutation Associated With Myoclonic Epilepsy With Ragged-Red Fibers and Other Neurological Features
2009 · Emma L. Blakely, S. Anand Trip, et al. · Archives of Neurology · 48
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Hypertrophic olivary degeneration on magnetic resonance imaging in mitochondrial syndromes associated with POLG and SURF1 mutations
2012 · K. J. Kinghorn, M. Kaliakatsos, et al. · Journal of Neurology · 47
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children
2009 · J D Stewart, S Tennant, et al. · Journal of Medical Genetics · 47
Respiratory Arrest: A Complication of Arnold-Chiari Malformation in Adults
2008 · Salah Omer, M. Zuheir Al-Kawi, et al. · European Neurology · 38
Myelopathy after intrathecal chemotherapy. A case report with unique magnetic resonance imaging changes
1994 · Donald R. McLean, Hugh M. Clink, et al. · Cancer · 38
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Upbeat nystagmus in anti-Ma2 encephalitis
2013 · Pablo Garcia-Reitboeck, Graham Thompson, et al. · Practical Neurology · 24
The wide POLG-related spectrum: An integrated view
2016 · M. Béreau, M. Anheim, et al. · Journal of the Neurological Sciences · 15
Hemichorea in systemic lupus erythematosus: significance of MRI findings
1995 · F. Al Jishi, M.Z. Al Kawi, et al. · Lupus · 14
Transient facial weakness whilst on a flight
2017 · Umesh Vivekananda, Salah Omer · Journal of the Neurological Sciences · 12
Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease
2016 · M. Muggenthaler, E. Petropoulou, et al. · International Journal of Cardiology · 9
The imploding antrum syndrome: an unusual cause of double vision
2010 · Karen Stevens, Salah Omer, et al. · Practical Neurology · 9
Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging
1995 · S. Bohlega, B. Stigsby, et al. · Movement Disorders · 8
Prominent cognitive decline and behavioural disturbance in late-onset Alexander disease
2015 · Pablo Garcia-Reitboeck, Andrew D. MacKinnon, et al. · Journal of the Neurological Sciences · 6
The Genetics of a Novel Form of Lafora Disease
2010 · Julie Turnbull, Jean‐Marie Girard, et al. · 5
Palatal Tremor: 12 Cases-the Experience of a Tertiary Neuroscience Centre
2016 · Nazia Karsan, Pablo Garcia Reitboeck, et al. · Journal of Neurology Neurosurgery & Psychiatry · 2
Potassium channel antibody associated encephalitis: A potentially treatable non-paraneoplastic limbic encephalitis
2004 · Jonathan M. Schott, A. Vincent, et al. · UCL Discovery (University College London) · 2
Book Review
2008 · J.M. Henderson, J.A. Ghika, et al. · European Neurology · 1
Mitochondrial DNA Deletion in Kearns-Sayre Syndrome: A Review and Illustration of Cases
1993 · Saeed Bohlega, M. Zuheir Al-Kawi, et al. · Annals of Saudi Medicine · 1
A case of congenital anosmia
2016 · Umesh Vivekananda, Nader Khandanpour, et al. · Neurology
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Adult Onset Alexander Disease: a Diagnosis to Consider in Late–onset Sporadic Spinocerebellar Ataxia
2013 · Vahini Paramesan, Andrew D MacKinnon, et al. · Journal of Neurology Neurosurgery & Psychiatry
Works count: 29
Citation count: 1,830
H-index: 13
I10-index: 14
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