Expanding the clinical, radiological and neuropathological phenotype of chronic lymphocytic inflammation with pontine perivascular enhancement responsive to …

NG Simon, JD Parratt, MH Barnett… - Journal of Neurology …, 2012 - jnnp.bmj.com
Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to
steroids (CLIPPERS) is a recently described inflammatory disease of the CNS with a …

Atypical inflammatory demyelinating syndromes of the CNS

TA Hardy, SW Reddel, MH Barnett, J Palace… - The Lancet …, 2016 - thelancet.com
Atypical inflammatory demyelinating syndromes are rare disorders that differ from multiple
sclerosis owing to unusual clinical or MRI findings or poor response to treatments used for …

[HTML][HTML] Neurological immunotherapy in the era of COVID-19—looking for consensus in the literature

C Korsukewitz, SW Reddel, A Bar-Or… - Nature reviews …, 2020 - nature.com
Abstract The coronavirus disease 2019 (COVID-19) pandemic is concerning for patients with
neuroimmunological diseases who are receiving immunotherapy. Uncertainty remains …

Clinical course, therapeutic responses and outcomes in relapsing MOG antibody-associated demyelination

S Ramanathan, S Mohammad, E Tantsis… - Journal of Neurology …, 2018 - jnnp.bmj.com
Objective We characterised the clinical course, treatment and outcomes in 59 patients with
relapsing myelin oligodendrocyte glycoprotein (MOG) antibody-associated demyelination …

Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis

S Ramanathan, K Prelog, EH Barnes… - Multiple Sclerosis …, 2016 - journals.sagepub.com
Background: Recognizing the cause of optic neuritis (ON) affects treatment decisions and
visual outcomes. Objective: We aimed to define radiological features of first-episode …

Regional variation of Guillain-Barré syndrome

AY Doets, C Verboon, B Van Den Berg, T Harbo… - Brain, 2018 - academic.oup.com
Guillain-Barré syndrome is a heterogeneous disorder regarding the clinical presentation,
electrophysiological subtype and outcome. Previous single country reports indicate that …

Antibodies to myelin oligodendrocyte glycoprotein in bilateral and recurrent optic neuritis

S Ramanathan, SW Reddel, A Henderson… - Neuroimmunology & …, 2014 - AAN Enterprises
Objective: We examined a cohort of adults with aquaporin-4 (AQP4) antibody–negative
neuromyelitis optica/neuromyelitis optica spectrum disorder (NMO/NMOSD) for antibodies to …

Use of whole-exome sequencing for diagnosis of limb-girdle muscular dystrophy: outcomes and lessons learned

R Ghaoui, ST Cooper, M Lek, K Jones, A Corbett… - JAMA …, 2015 - jamanetwork.com
Importance To our knowledge, the efficacy of transferring next-generation sequencing from a
research setting to neuromuscular clinics has never been evaluated. Objective To translate …

Anti‐MuSK patient antibodies disrupt the mouse neuromuscular junction

RN Cole, SW Reddel, OL Gervásio… - Annals of Neurology …, 2008 - Wiley Online Library
Objective A subset of myasthenia gravis patients that are seronegative for anti‐acetylcholine
receptor (anti‐AChR) antibodies are instead seropositive for antibodies against the muscle …

Incidence and prevalence of NMOSD in Australia and New Zealand

W Bukhari, KM Prain, P Waters, M Woodhall… - Journal of Neurology …, 2017 - jnnp.bmj.com
Objectives We have undertaken a clinic-based survey of neuromyelitis optica spectrum
disorders (NMOSDs) in Australia and New Zealand to establish incidence and prevalence …