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Top Articles

#TitleJournalYearCitations
1Clinical and pathological features of a parkinsonian syndrome in a family with an Ala53Thr ?-synuclein mutationAnnals of Neurology2001364
2Cortical excitability distinguishes ALS from mimic disordersClinical Neurophysiology2011122
3Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P2 phosphatase FIG4Brain2011107
4Split-hand index for the diagnosis of amyotrophic lateral sclerosisClinical Neurophysiology201397
5Anti-melanin antibodies are increased in sera in Parkinson's diseaseExperimental Neurology200972
6Interrelationship of Optical Coherence Tomography and Multifocal Visual-Evoked Potentials after Optic NeuritisExperimental Neurology201068
7Basilar impression complicating osteogenesis imperfecta type IV: the clinical and neuroradiological findings in four casesJournal of Neurology, Neurosurgery and Psychiatry199961
8Neurological immunotherapy in the era of COVID-19 — looking for consensus in the literatureNature Reviews Neurology202057
9Cortical dysfunction underlies disability in multiple sclerosisMultiple Sclerosis Journal201256
10COVID-19 in teriflunomide-treated patients with multiple sclerosisJournal of Neurology202056
11The contribution of tremor studies to diagnosis of Parkinsonian and essential tremor: a statistical evaluationJournal of Clinical Neuroscience200250
12Guillain-Barré Syndrome: Modern Theories of EtiologyCurrent Allergy and Asthma Reports201150
13Diagnostic utility of cortical excitability studies in amyotrophic lateral sclerosisEuropean Journal of Neurology201444
14Mortality and Causes of Death in Patients with Sporadic Inclusion Body Myositis: Survey Study Based on the Clinical Experience of Specialists in Australia, Europe and the USAJournal of Neuromuscular Diseases201644
15Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypesParkinsonism and Related Disorders201944
16Managing the risks of immunosuppressionCurrent Opinion in Neurology201141
17Inner Nuclear Layer Thickening Is Inversley Proportional to Retinal Ganglion Cell Loss in Optic NeuritisPLoS ONE201339
18Association of Maintenance Intravenous Immunoglobulin With Prevention of Relapse in Adult Myelin Oligodendrocyte Glycoprotein Antibody–Associated DiseaseJAMA Neurology202239
19Current concepts in the management of Parkinson diseaseMedical Journal of Australia201037
20Axonal Ion Channel Dysfunction inC9orf72Familial Amyotrophic Lateral SclerosisJAMA Neurology201535
21Distinguishing Susac’s syndrome from multiple sclerosisJournal of Neurology201534
22High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: An analysis of disease-associated alleles and diplotypesJournal of Neuroimmunology201231
23Athetosis I: Historical considerationsMovement Disorders200230
24Corticomotoneuronal function and hyperexcitability in acquired neuromyotoniaBrain201029
25The utility of multimodal evoked potentials in multiple sclerosis prognosticationJournal of Clinical Neuroscience201329
26Athetosis II: The syndrome of mild athetoid cerebral palsyMovement Disorders200227
27Myosin storage (hyaline body) myopathy: A case reportNeuromuscular Disorders200626
28Significance of Myelin Oligodendrocyte Glycoprotein Antibodies in CSFNeurology202322
29Parallel Changes in Structural and Functional Measures of Optic Nerve Myelination after Optic NeuritisPLoS ONE201521
30Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositisJournal of Neuroimmunology201320
31Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptomsNeuromuscular Disorders201318
32Pretreatment and posttreament positron emission tomographic scan imaging in a 20-year-old patient with Wilson's diseaseMovement Disorders199817
33Diagnosis, differential diagnosis and misdiagnosis of Susac syndromeEuropean Journal of Neurology202216
34Apolipoprotein ε alleles in sporadic inclusion body myositis: A reappraisalNeuromuscular Disorders200815
35Sarcolemmal excitability in the myotonic dystrophiesMuscle and Nerve201812
36The neuro-otology of Susac syndromeJournal of Neurology202011
37Successful implementation of an automated electronic support system for patient safety monitoring: The alemtuzumab in multiple sclerosis safety systems (AMS3) studyMultiple Sclerosis Journal20197
38Mechanism of delayed conduction of fellow eyes in patients with optic neuritisInternational Journal of Ophthalmology20186
39Association between musk antibody concentrations and the myasthenia gravis composite score in 3 patients: A marker of relapse?Muscle and Nerve20196
40Clinical and pathological features of a parkinsonian syndrome in a family with an Ala53Thr α-synuclein mutationMuscle and Nerve20016
41Handgrip Maximal Voluntary Isometric Contraction Does Not Correlate with Thenar Motor Unit Number EstimationNeurology Research International20125
42Enhanced serum immunoglobulin G clearance in myotonic dystrophy-associated hypogammaglobulinemia: a case series and review of the literatureJournal of Medical Case Reports20195
43Tumefactive demyelination: updated perspectives on diagnosis and managementExpert Review of Neurotherapeutics20215
44Distinguishing CNS neurosarcoidosis from multiple sclerosis and an approach to “overlap” casesJournal of Neuroimmunology20225
45AN EVALUATION OF SIGNS IN OCULAR MYASTHENIA GRAVIS AND CORRELATION WITH ACETYLCHOLINE RECEPTOR ANTIBODIESAustralian and New Zealand Journal of Ophthalmology19854
46Compressive Lateral Femoral Cutaneous Neuropathy Secondary to Sartorius Muscle FibrosisJAMA Neurology20194
47Prospective growth and developmental outcomes in infants born to mothers with multiple sclerosisMultiple Sclerosis Journal20214
48Anticipation of onset age in familial Parkinson's disease without SCA gene mutationsParkinsonism and Related Disorders20063
49Longitudinal improvement in neuropsychological profile following treatment of severe encephalopathy in Susac syndromeNeuroimmunology Reports20212
50439: Detection of large-scale deletions in mitochondrial DNA using DNA extracted from salivary samplesJournal of Clinical Neuroscience20080