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Aldo Quattrone

Researcher Next ID · RN-029003

Researcher · Medicine

Magna Graecia University

Catanzaro, Austria

Not currently recruitingFunding unknown
Works count
896
Citation count
32,244
H-index
79
i10-index
508

Research interests

Medicine
Neuroscience
Parkinson's Disease Mechanisms and Treatments
Neurological disorders and treatments
Epilepsy research and treatment
Hereditary Neurological Disorders
Genetic Neurodegenerative Diseases

Publications

  • Random Forest Algorithm for the Classification of Neuroimaging Data in Alzheimer's Disease: A Systematic Review

    Frontiers in Aging Neuroscience · 2017 · 10.3389/fnagi.2017.00329

  • The challenge of mapping the human connectome based on diffusion tractography

    Nature Communications · 2017 · https://doi.org/10.1038/s41467-017-01285-x

  • Magnetic resonance imaging biomarkers for the early diagnosis of Alzheimer's disease: a machine learning approach

    Frontiers in Neuroscience · 2015 · 10.3389/fnins.2015.00307

  • Machine learning on brain MRI data for differential diagnosis of Parkinson's disease and Progressive Supranuclear Palsy

    Journal of Neuroscience Methods · 2013 · 10.1016/j.jneumeth.2013.11.016

  • A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

    JAMA Neurology · 2013 · 10.1001/jamaneurol.2013.1925

  • Mutation in theSYNJ1Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

    Human Mutation · 2013 · 10.1002/humu.22373

  • Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

    Brain · 2012 · 10.1093/brain/awr366

  • Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial

    The Lancet Neurology · 2011 · 10.1016/s1474-4422(11)70025-4

  • Patterns of brain atrophy in Parkinson’s disease, progressive supranuclear palsy and multiple system atrophy

    Parkinsonism & Related Disorders · 2011 · 10.1016/j.parkreldis.2010.12.010

  • Neuroanatomic correlates of psychogenic nonepileptic seizures: A cortical thickness and VBM study

    Epilepsia · 2011 · 10.1111/j.1528-1167.2011.03347.x

  • Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

    The Lancet Neurology · 2011 · 10.1016/s1474-4422(11)70175-2

  • Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

    New England Journal of Medicine · 2009 · https://doi.org/10.1056/nejmoa0901281

  • Essential Head Tremor Is Associated with Cerebellar Vermis Atrophy: A Volumetric and Voxel-Based Morphometry MR Imaging Study

    American Journal of Neuroradiology · 2008 · 10.3174/ajnr.a1190

  • MR Imaging Index for Differentiation of Progressive Supranuclear Palsy from Parkinson Disease and the Parkinson Variant of Multiple System Atrophy

    Radiology · 2007 · 10.1148/radiol.2453061703

  • Sex Differences in Clinical and Genetic Determinants of Levodopa Peak-Dose Dyskinesias in Parkinson Disease

    Archives of Neurology · 2005 · 10.1001/archneur.62.4.601

  • DJ‐1 mutations and parkinsonism‐dementia‐amyotrophic lateral sclerosis complex

    Annals of Neurology · 2005 · 10.1002/ana.20666

  • Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity

    Biological Psychiatry · 2005 · 10.1016/j.biopsych.2005.07.027

  • Identification of an Na v 1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures

    Proceedings of the National Academy of Sciences · 2005 · 10.1073/pnas.0506818102

  • Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

    Nature Genetics · 2004 · https://doi.org/10.1038/ng1341

  • UCHL1 is a Parkinson's disease susceptibility gene

    Annals of Neurology · 2004 · 10.1002/ana.20017

  • Quetiapine and Clozapine in Parkinsonian Patients With Dopaminergic Psychosis

    Clinical Neuropharmacology · 2004 · 10.1097/01.wnf.0000136891.17006.ec

  • Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders

    Nature Genetics · 2003 · 10.1038/ng1145

  • The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy

    Nature Genetics · 2000 · 10.1038/81566

  • Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2

    Nature Genetics · 2000 · 10.1038/75542

  • Prolactin secretion in man: a useful tool to evaluate the activity of drugs on central 5‐hydroxytryptaminergic neurones. Studies with fenfluramine.

    British Journal of Clinical Pharmacology · 1983 · 10.1111/j.1365-2125.1983.tb02202.x

Current projects

    No projects listed.