Not Specified

• 15 years of Niemann Pick C in Australia
• A Case of Cerebral Vasculitis Due to Giant Cell Arteritis
• A Case Series of Intra-arterial Embolectomy for Acute Ischemic Stroke
• Age over 80 or Leukoaraiosis Do Not Predict Hemorrhagic transformation after tPA for ischemic stroke
• Alterations to White Matter Microstructure and Grey Matter Volume in Adult Niemann-Pick Type C
• Amyloid Angiopathy Presenting as Convexity SAH and Heralding Lobar Haemorrhage: Clinical, Imaging and Biopsy Features
• Antiepileptic Drug Polytherapy Issues in Pregnancy
• Audiovestibular Sarcoidosis
• Australian Motor Neuron Disease Registry 5 year Follow-Up
• Benign Infantile Cytochrome c oxidase Deficiency Myopathy: Reversible or Not?
• Bilateral Frontal Periventricular Locations of Cerebral White Matter Lesions show Greatest Covariance with Poorer Gait
• Case Report on Fatal Familial Insomnia Associated with Myelodysplasia Due to Chromosome 20q Deletion
• Central Mechanisms Underlying Fatigue in Amyotrophic Lateral Sclerosis
• Clinical and Radiological Features, Management and Outcome After Vertebrobasilar Dissection
• Clinical Characteristics of Aquaporin 4 Auto-antibody Positive Patients – A Case Series
• Clinical Features of Patients with Demyelinating Neuropathy Associated with Anti-MAG Antibody
• Clinical Trial of Levetiracetam for Dyskinesia in Parkinson’s Disease
• Developmental Hip Abnormalities In Paediatric CMT
• Distinct, Isolated Bulbar Palsy Presentations of Amyotrophic Lateral sclerosis
• Disturbances in Axonal Function in Patients with Erythromelalgia
• Does the Principle of Minimum Work Apply at the Carotid Bifurcation?
• Dural Ectasia in Marfan’s Syndrome: Clinical and MRI Features
• Effect of Large Scale Stroke Unit Implementation on One Year Ischaemic Stroke Out
• Endarterectomy for “Hemodynamically Insignificant” Symptomatic Carotid Stenosis
• Epidermolysis Bullosa with Late-Onset Muscular Dystrophy and Plectin Deficiency
• Final Infarct Volume Can Be Determined Using Diffusion Imaging 24 Hours After Stroke Onset
• FLAIR Hyperintensity in Acute Ischemic Strokes Beyond 3 Hours is Almost Universal and Does Not Predict Hemorrhagic Transformation
• Genetic Influences of Sigma-1 Receptor and Apolipoprotein E on the Severity of Alzheimer’s Disease
• HLA-DRB1 Alleles are Determinants of Spinal Cord Pathology in Multiple Sclerosis (MS)
• Hydroxychloroquine Induced Vacuolar Myopathy Mimicking Acid Maltase
• Hyperpolarisation of Motor Axons in Inclusion Body Myopathy, Paget’s Disease of the Bone and Frontotemporal Dementia (IBMPFD)
• Hypothalamic Lesions and Association with HLA-DRB1 alleles in Multiple Sclerosis (MS) and Neuromyelitis Optica (NMO)
• Impulse Control Disorders and the Quality of Life in Parkinson’s Disease
• Increased Cannabis Use in Young Stroke Patients
• Intrastriatal Transplantation of Human Olfactory Neuroepithelial Cells Attenuates the Striatal Pathology in a Transgenic Model of Huntington’s Disease
• Intravenous Lignocaine Infusion for Prolonged, Resistant Headache
• Is There Ongoing Loss of Nerve Cells in Subjects Exposed to Thalidomide in Utero?
• KONQUEST: Keppra versus Older AEDS and Neuropsychiatric, Neurocognitive and QUality of life outcomes in treatment of Epilepsy as Substitution monoTherapy
• Longitudinal Employment Change in Multiple Sclerosis and the Importance of Symptom Management
• Major Infarct Growth Beyond 3-6 Hours is Associated with Failure of Collateral Circulation
• Management and Outcomes of Patients with Mitochondrial Disorders Requiring Critical Care Admissions
• Mechanisms of Neurodegeneration in Spinal Muscular Atrophy
• Mitochondrial Abnormalities in a New Cell Model of MNGIE Syndrome
• Modulation of Regulatory and Cytotoxic T Cell Expression Signature in First Demyelinating Events and Early Multiple Sclerosis
• Mutations in PARK9 (ATP13A2) causing Kufor-Rakeb Syndrome, Provide Insights into Cellular Dysfunction in Parkinson's Disease
• Neuroferritinopathy
• Neuropathy: An Integral Component of Cerebellar Ataxia Neuropathy Vestibular Areflexia Syndrome
• Neuropsychiatric Features in Motor Neurone Disease (MND) vs. Behavioural Variant Frontotemporal Dementia (bvFTD)
• Novel Upper and Lower Motor Neurone Markers of ALS
• On the Shoulders of Giants: The Brain Foundation 1970-2010
• Penumbral Imaging with Computed Tomography Perfusion in an Experimental Model of Acute Stroke
• Peripheral Nerve Excitability Testing Shows Distinctive Ion Channel Dysfunction in Patients with KCNQ2 Mutations and Epilepsy
• Regionally Specific Diffusion Tensor Imaging in Mild Cognitive Impairment and Alzheimer's Disease
• Respiratory Involvement in Inherited Neuropathies in Children
• Rotenone Toxicity in Parkin Mutated Olfactory Cell Cultures
• Silver Syndrome: A Case Report
• Spontaneous Intracranial Hypotension in Childhood: A Case Report and Review of the Literature
• Susac’s Syndrome Responds to the Tumour Necrosis Factor (TNF) Inhibitor, Infliximab
• Systematic Review of the Effect Coffee on Parkinson Disease Risk
• The Clinical Utility of Romberg's Test
• The Getting of Wisdom: A History of the Neurological Textbook
• The Origin of the Neurology Department at Auckland Hospital
• The Role of ABCD2 in Predicting Stroke Recurrence in the Australian Setting
• Time Frequency Mapping of the Rhythmic Limb Movements Reliably Distinguishes Convulsive Epileptic from Psychogenic Non-epileptic Seizures
• Transient Ischaemic Attack Mimic Secondary to Acute Convexity subarachnoid haemorrhage
• Transverse Sinus Stenting in Pseudotumor Cerebri
• Unusual Clinical Presentations Associated with the A3243G Mutation
• Use of Pre-trial Cognitive Trajectory to Accelerate Primary Prevention Trials of Disease-modifying Therapies in AD
• Use of the Addenbrooke's Cognitive Examination in Multiple Sclerosis
• Worse Stroke Outcome in Patients with Atrial Fibrillation May Be Due to Greater Volumes of More Severe Hypoperfusion

70 abstracts