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Publications

Prodromal headache in MOG-antibody positive optic neuritis.

Asseyer S. et al, (2020), Mult Scler Relat Disord, 40

'LESS CONTENTED AS A PERSON': AN UPDATE FROM THE LGI1-QOL STUDY

Binks S. et al, (2019), JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 90, E34 - E34

Thymoma-associated myasthenia gravis and LGI1-encephalitis, with nephrotic syndrome post-thymectomy

Hor JY. et al, (2018), Journal of Neuroimmunology, 317, 100 - 102

Prevalence of neuromyelitis optica spectrum disorder in the multi-ethnic Penang Island, Malaysia, and a review of worldwide prevalence

Hor JY. et al, (2018), Multiple Sclerosis and Related Disorders, 19, 20 - 24

Inflammatory myopathy associated with myasthenia gravis with and without thymic pathology: Report of four cases and literature review

Santos E. et al, (2017), Autoimmunity Reviews, 16, 644 - 649

Chronic neuropathic pain severity is determined by lesion level in aquaporin 4-antibody-positive myelitis

Tackley G. et al, (2017), Journal of Neurology, Neurosurgery & Psychiatry, 88, 165 - 169

Epidemiology of myasthenia gravis in Northern Portugal: Frequency estimates and clinical epidemiological distribution of cases

Santos E. et al, (2016), Muscle & Nerve, 54, 413 - 421

Pain in patients with transverse myelitis and its relationship to aquaporin 4 antibody status

Kong Y. et al, (2016), Journal of the Neurological Sciences, 368, 84 - 88

Search for new phenomena in final states with an energetic jet and large missing transverse momentum inppcollisions ats=13 TeVusing the ATLAS detector

Aaboud M. et al, (2016), Physical Review D, 94

Pregnancy outcomes in aquaporin-4–positive neuromyelitis optica spectrum disorder

Nour MM. et al, (2016), Neurology, 86, 79 - 87

Congenital myasthenic syndrome due to mutation in CHRNE gene with clinical worsening and thymic hyperplasia attributed to association with autoimmune-myasthenia gravis

Santos E. et al, (2015), Neuromuscular Disorders, 25, 928 - 931

Aquaporin-4 antibody isoform binding specificities do not explain clinical variations in NMO

Kitley J. et al, (2015), Neurology - Neuroimmunology Neuroinflammation, 2, e121 - e121

Predictive value of MRI parameters in severity and recovery of first-episode myelitis in aquaporin-4 antibody disease

Murchison A. et al, (2015), Journal of the Neurological Sciences, 355, 49 - 53

Update on biomarkers in neuromyelitis optica

Melamed E. et al, (2015), Neurology - Neuroimmunology Neuroinflammation, 2, e134 - e134

Use of Advanced Magnetic Resonance Imaging Techniques in Neuromyelitis Optica Spectrum Disorder

Kremer S. et al, (2015), JAMA Neurology, 72, 815 - 815

A 41-year-old woman with acute weakness and encephalopathy associated with MOG antibodies

Morris KA. et al, (2015), Neurology - Neuroimmunology Neuroinflammation, 2, e88 - e88

Clinical Features and Diagnostic Usefulness of Antibodies to Clustered Acetylcholine Receptors in the Diagnosis of Seronegative Myasthenia Gravis

Rodríguez Cruz PM. et al, (2015), JAMA Neurology, 72, 642 - 642

Demographic and clinical features of neuromyelitis optica: A review

Pandit L. et al, (2015), Multiple Sclerosis Journal, 21, 845 - 853

MOG cell-based assay detects non-MS patients with inflammatory neurologic disease

Waters P. et al, (2015), Neurology - Neuroimmunology Neuroinflammation, 2, e89 - e89

Myasthenia gravis: Association of British Neurologists’ management guidelines

Sussman J. et al, (2015), Practical Neurology, 15, 199 - 206

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