# | Title | Journal | Year | Citations |
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1 | Non-invasive electrical and magnetic stimulation of the brain, spinal cord, roots and peripheral nerves: Basic principles and procedures for routine clinical and research application. An updated report from an I.F.C.N. Committee | Clinical Neurophysiology | 2015 | 1,957 |
2 | Phenomenology and classification of dystonia: A consensus update | Movement Disorders | 2013 | 1,754 |
3 | Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1 | Nature Genetics | 2013 | 589 |
4 | Vestibular evoked myogenic potentials: Past, present and future | Clinical Neurophysiology | 2010 | 471 |
5 | A double‐blind, placebo‐controlled study to assess the mitochondria‐targeted antioxidant MitoQ as a disease‐modifying therapy in Parkinson's disease | Movement Disorders | 2010 | 467 |
6 | Bilateral vestibulopathy: Diagnostic criteria Consensus document of the Classification Committee of the Bárány Society1 | Journal of Vestibular Research: Equilibrium and Orientation | 2017 | 364 |
7 | Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis | Multiple Sclerosis Journal | 2016 | 284 |
8 | A proposal for new diagnostic criteria for ALS | Clinical Neurophysiology | 2020 | 268 |
9 | Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force | Movement Disorders | 2016 | 228 |
10 | European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society | European Journal of Neurology | 2006 | 224 |
11 | Safety of Converting From Tetrabenazine to Deutetrabenazine for the Treatment of Chorea | JAMA Neurology | 2017 | 209 |
12 | Inflammatory infiltrates in sural nerve biopsies in Guillain-Barr� syndrome and chronic inflammatory demyelinating neuropathy | | 1996 | 178 |
13 | Clinical and Biomarker Changes in Premanifest Huntington Disease Show Trial Feasibility: A Decade of the PREDICT-HD Study | Frontiers in Aging Neuroscience | 2014 | 177 |
14 | Phosphorylated tau interactome in the human Alzheimer’s disease brain | Brain | 2020 | 171 |
15 | Effect of Intravenous Tenecteplase Dose on Cerebral Reperfusion Before Thrombectomy in Patients With Large Vessel Occlusion Ischemic Stroke | JAMA - Journal of the American Medical Association | 2020 | 168 |
16 | Three simple clinical tests to accurately predict falls in people with Parkinson's disease | Movement Disorders | 2013 | 167 |
17 | Emerging therapies and challenges in spinal muscular atrophy | Annals of Neurology | 2017 | 157 |
18 | Disorders of the autonomic nervous system: Part 2. investigation and treatment | Annals of Neurology | 1987 | 150 |
19 | Axonal loss and myelin in early ON loss in postacute optic neuritis | Annals of Neurology | 2008 | 144 |
20 | Single blind randomised controlled trial of GAME (Goals Activity Motor Enrichment) in infants at high risk of cerebral palsy | Research in Developmental Disabilities | 2016 | 142 |
21 | Electrophysiological studies in the Guillain-Barr� syndrome | Annals of Neurology | 1981 | 139 |
22 | Impact of the COVID‐19 Pandemic on Parkinson's Disease and Movement Disorders | Movement Disorders | 2020 | 134 |
23 | Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy | Brain | 2015 | 128 |
24 | Disorders of the autonomic nervous system: Part 1. Pathophysiology and clinical features | Annals of Neurology | 1987 | 124 |
25 | Standards for Detecting, Interpreting, and Reporting Noncontrast Computed Tomographic Markers of Intracerebral Hemorrhage Expansion | Annals of Neurology | 2019 | 121 |
26 | Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P2 phosphatase FIG4 | Brain | 2011 | 107 |
27 | Pathophysiological Insights Derived by Natural History and Motor Function of Spinal Muscular Atrophy | Journal of Pediatrics | 2013 | 104 |
28 | Fatigue in multiple sclerosis: Mechanisms and management | Clinical Neurophysiology | 2010 | 97 |
29 | Differentiating lower motor neuron syndromes | Journal of Neurology, Neurosurgery and Psychiatry | 2017 | 93 |
30 | The effect of ageing on autonomic nervous system function | Australian and New Zealand Journal of Medicine | 1990 | 90 |
31 | Optimising motor learning in infants at high risk of cerebral palsy: a pilot study | BMC Pediatrics | 2015 | 89 |
32 | Protein and peptide fractionation, enrichment and depletion: Tools for the complex proteome | Proteomics | 2011 | 88 |
33 | Assessment of patients with isolated or combined dystonia: An update on dystonia syndromes | Movement Disorders | 2013 | 88 |
34 | Huntingtonʼs disease | Current Opinion in Neurology | 2012 | 87 |
35 | Upregulation of persistent sodium conductances in familial ALS | Journal of Neurology, Neurosurgery and Psychiatry | 2010 | 86 |
36 | Diagnostic contribution and therapeutic perspectives of transcranial magnetic stimulation in dementia | Clinical Neurophysiology | 2021 | 85 |
37 | Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies | Movement Disorders | 2014 | 79 |
38 | Consensus guidelines for the investigation and management of encephalitis in adults and children in Australia and New Zealand | Internal Medicine Journal | 2015 | 76 |
39 | Multifocal VEP and OCT in optic neuritis: a topographical study of the structure–function relationship | Documenta Ophthalmologica | 2009 | 75 |
40 | Noninvasive Cerebrovascular Autoregulation Assessment in Traumatic Brain Injury: Validation and Utility | Journal of Neurotrauma | 2003 | 74 |
41 | Defining the mechanisms that underlie cortical hyperexcitability in amyotrophic lateral sclerosis | Experimental Neurology | 2009 | 71 |
42 | Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy | Journal of Molecular Medicine | 2013 | 70 |
43 | Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing | Science Advances | 2022 | 68 |
44 | The effects of alterations in conditioning stimulus intensity on short interval intracortical inhibition | Brain Research | 2009 | 67 |
45 | Myotonic dystrophy and the heart: A systematic review of evaluation and management | International Journal of Cardiology | 2015 | 66 |
46 | GAME (Goals - Activity - Motor Enrichment): protocol of a single blind randomised controlled trial of motor training, parent education and environmental enrichment for infants at high risk of cerebral palsy | BMC Neurology | 2014 | 64 |
47 | Immunopathological factors in peripheral nerve allograft rejection: Quantification of lymphocyte invasion and major histocompatibility complex expression | Journal of the Neurological Sciences | 1990 | 63 |
48 | Safety and tolerability of Triumeq in amyotrophic lateral sclerosis: the Lighthouse trial | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | 2019 | 63 |
49 | Measurement of axonal excitability: Consensus guidelines | Clinical Neurophysiology | 2020 | 63 |
50 | Susac syndrome: Microangiopathy of the retina, cochlea and brain | Clinical and Experimental Ophthalmology | 2000 | 60 |