Pietro Cortelli

Research interests

Publications

• The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy

  Movement Disorders · 2022 · 10.1002/mds.29005

• Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies

  Acta Neuropathologica · 2020 · https://doi.org/10.1007/s00401-020-02160-8

• Risk and predictors of dementia and parkinsonism in idiopathic REM sleep behaviour disorder: a multicentre study

  Brain · 2019 · https://doi.org/10.1093/brain/awz030

• Consensus statement on the definition of neurogenic supine hypertension in cardiovascular autonomic failure by the American Autonomic Society (AAS) and the European Federation of Autonomic Societies (EFAS)

  Clinical Autonomic Research · 2018 · https://doi.org/10.1007/s10286-018-0529-8

• Noninvasive vagus nerve stimulation as acute therapy for migraine

  Neurology · 2018 · https://doi.org/10.1212/wnl.0000000000005857

• Brain–heart interactions: physiology and clinical implications

  Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · 2016 · https://doi.org/10.1098/rsta.2015.0181

• Cost of healthcare for patients with migraine in five European countries: results from the International Burden of Migraine Study (IBMS)

  The Journal of Headache and Pain · 2012 · https://doi.org/10.1007/s10194-012-0460-7

• Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome

  Clinical Autonomic Research · 2011 · https://doi.org/10.1007/s10286-011-0119-5

• Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome

  Autonomic Neuroscience · 2011 · https://doi.org/10.1016/j.autneu.2011.02.004

• Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

  Science · 2009 · https://doi.org/10.1126/science.1166066

• Guidelines for the diagnosis and management of syncope (version 2009): The Task Force for the Diagnosis and Management of Syncope of the European Society of Cardiology (ESC)

  European Heart Journal · 2009 · https://doi.org/10.1093/eurheartj/ehp298

• EFNS guidelines on the diagnosis and management of orthostatic hypotension

  European Journal of Neurology · 2006 · https://doi.org/10.1111/j.1468-1331.2006.01512.x

• Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians

  European Journal of Human Genetics · 2005 · https://doi.org/10.1038/sj.ejhg.5201425

• Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

  Science · 2004 · https://doi.org/10.1126/science.1096284

• Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy

  Ophthalmology · 2004 · https://doi.org/10.1016/j.ophtha.2004.06.034

• Familial and sporadic fatal insomnia

  The Lancet Neurology · 2003 · https://doi.org/10.1016/s1474-4422(03)00323-5

• Sympathetic skin response

  Clinical Autonomic Research · 2003 · https://doi.org/10.1007/s10286-003-0107-5

• REM sleep behavior disorders in multiple system atrophy

  Neurology · 1997 · https://doi.org/10.1212/wnl.48.4.1094

• Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity

  Science · 1996 · https://doi.org/10.1126/science.274.5295.2079

• Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.

  Proceedings of the National Academy of Sciences · 1994 · https://doi.org/10.1073/pnas.91.7.2839

• Fatal familial insomnia

  Neurology · 1992 · https://doi.org/10.1212/wnl.42.3.669

• Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

  Science · 1992 · https://doi.org/10.1126/science.1439789

• Abnormal brain and muscle energy metabolism shown by 31 P magnetic resonance spectroscopy in patients affected by migraine with aura

  Neurology · 1992 · https://doi.org/10.1212/wnl.42.6.1209

• Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

  New England Journal of Medicine · 1992 · https://doi.org/10.1056/nejm199202133260704

• Fatal Familial Insomnia and Dysautonomia with Selective Degeneration of Thalamic Nuclei

  New England Journal of Medicine · 1986 · https://doi.org/10.1056/nejm198610163151605

Current projects

No projects listed.