John Merory

The Royal Melbourne Hospital — Australia

Neuroscience · Life Sciences

15h-index2.3kcitations26works0.02yr avg
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Research Topics

Hereditary Neurological Disorders(5), Balance, Gait, and Falls Prevention(4), Traumatic Brain Injury and Neurovascular Disturbances(4), Dementia and Cognitive Impairment Research(3), Cerebrovascular and Carotid Artery Diseases(3)

Publications26 total

Rates of age‐ and amyloid β‐associated cortical atrophy in older adults with superior memory performance
Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring·2019· 24 citedOpen Access
The <sup>18</sup>F-FDG PET Cingulate Island Sign and Comparison to <sup>123</sup>I-β-CIT SPECT for Diagnosis of Dementia with Lewy Bodies
Journal of Nuclear Medicine·2009· 296 citedOpen Access
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
Brain·2009· 92 citedOpen Access
Cognition and performance of everyday tasks in mild to moderate Parkinson's Disease.
CentAUR (University of Reading)·2008
Imaging β-amyloid burden in aging and dementia
Neurology·2007· 1.1k cited
Physiological Falls Risk Assessment in Older People with Alzheimer’s Disease
Dementia and Geriatric Cognitive Disorders·2007· 50 cited
Quantitative gait analysis in patients with dementia with Lewy bodies and Alzheimer's disease
Gait & Posture·2006· 69 cited
P1–151: Gait variability in Alzheimer's disease
Alzheimer s & Dementia·2006
Gait Variability in Community Dwelling Adults With Alzheimer Disease
Alzheimer Disease & Associated Disorders·2006· 121 cited
Mutations in the Pleckstrin Homology Domain of Dynamin 2 Cause Dominant Intermediate Charcot-Marie-Tooth Disease
Neurology·2005· 4 cited
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease
Nature Genetics·2005· 356 cited
P1-053 GAIT analysis in dementias
Neurobiology of Aging·2004
FDG-PET and dopamine and serotonin transporter SPECT to distinguish dementia with Lewy bodies from Alzheimer's disease
ANZ nuclear medicine·2004
Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region
Neurogenetics·2003· 9 cited
Dominant Intermediate Charcot-Marie-Tooth Neuropathy Maps to Chromosome 19p12-p13.2
The American Journal of Human Genetics·2001· 48 citedOpen Access
Doppler diagnosis in cases of acute stroke
The Medical Journal of Australia·1989· 4 cited
Subcortical arteriosclerotic encephalopathy: Binswanger's disease.
PubMed·1987· 15 cited
INTRAVENOUS PULSE METHYL PREDNISOLONE IN THE SUCCESSFUL TREATMENT OF SEVERE SARCOID POLYNEUROPATHY WITH PULMONARY INVOLVEMENT
Australian and New Zealand Journal of Medicine·1985· 10 cited
ADRENOMYELONEUROPATHY–CLINICAL and BIOCHEMICAL DIAGNOSIS
Australian and New Zealand Journal of Medicine·1983· 22 cited
Cerebral blood flow after surgery for recent subarachnoid haemorrhage
Journal of Neurology Neurosurgery & Psychiatry·1980· 25 citedOpen Access
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Frequent Co-authors

Marina Kennerson(5), Garth A. Nicholson(5), Joanne E. Wittwer(5), Mark Woodward(4), Danqing Zhu(4), Victor L. Villemagne(3), Stephan Züchner(3), Kristl G. Claeys(3), Peter De Jonghe(3), Vincent Timmerman(3), Jeffery M. Vance(3), Christopher C. Rowe(3), Kate E. Webster(3), Paul Maruff(2), Colin L. Masters(2), Maher Noureddine(2), Kristien Verhoeven(2), Sofia A. Oliveira(2), Marcy C. Speer(2), Judith E. Stenger(2)