N. Checcarelli

发表

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy

N. Bresolin, G. Comi, G. Scarlato, 1994, Journal of the Neurological Sciences.

The role of clinical and neuroimaging features in the diagnosis of CADASIL

E. Parati, P. Vitali, G. Comi, 2018, Journal of Neurology.

Migraine and Cryptogenic Ischemic Stroke

R. Calabró, A. Adami, A. Padovani, 2020, Annals of neurology.

Propensity Score–Based Analysis of Percutaneous Closure Versus Medical Therapy in Patients With Cryptogenic Stroke and Patent Foramen Ovale: The IPSYS Registry (Italian Project on Stroke in Young Adults)

R. Calabró, A. Adami, L. Iacoviello, 2016, Circulation. Cardiovascular interventions.

Critically ill patients: immunological evidence of inflammation in muscle biopsy.

S. Barbieri, P. Tonin, G. Scarlato, 1999, Clinical neuropathology.

An unusual cause of ischemic stroke with successful thrombolysis.

G. Corrado, P. Panisi, N. Checcarelli, 2013, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

History of Migraine and Volume of Brain Infarcts: The Italian Project on Stroke at Young Age (IPSYS)

A. Padovani, M. Zedde, R. Pascarella, 2019, Journal of stroke.

Left Ventricular Hypertrabeculation/Noncompaction with PMP22 Duplication-Based Charcot-Marie-Tooth Disease Type 1A

J. Finsterer, C. Stöllberger, G. Corrado, 2006, Cardiology.

Determinants of premature familial arterial thrombosis in patients with juvenile ischaemic stroke

R. Calabró, A. Adami, L. Iacoviello, 2014, Thrombosis and Haemostasis.

Assay of mitochondrial ATP synthesis in animal cells.

A. Spinazzola, G. Manfredi, A. Naini, 2001, Methods in cell biology.

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

S. Dimauro, E. Schon, F. Santorelli, 2002, Biochemical and biophysical research communications.

Appearance and localization of dystrophin in normal human fetal muscle

G. Comi, E. Scarpini, G. Scarlato, 1991, International Journal of Developmental Neuroscience.

Desmin and Vimentin as markers of regeneration in muscle diseases

G. Scarlato, M. Moggio, A. Prelle, 2004, Acta Neuropathologica.

Differential features of patients with mutations in two COX assembly genes, SURF‐1 and SCO2

P. Kaplan, S. Dimauro, L. Papadopoulou, 2000, Annals of neurology.

Association Between Migraine and Cervical Artery Dissection: The Italian Project on Stroke in Young Adults

R. Calabró, A. Adami, L. Iacoviello, 2017, JAMA neurology.

Multiple sclerosis and mitochondrial myopathy: An unusual combination of diseases

N. Bresolin, E. Scarpini, G. Scarlato, 1994, Journal of Neurology.

Congenital myopathy associated with abnormal accumulation of desmin and dystrophin

N. Bresolin, G. Comi, G. Scarlato, 1992, Neuromuscular Disorders.

A Missense Mutation in the Mitochondrial Cytochrome b Gene in a Revisited Case with Histiocytoid Cardiomyopathy

S. Dimauro, A. Andreu, S. Shanske, 2000, Pediatric Research.

Mitochondrial DNA abnormalities and autistic spectrum disorders.

S. Dimauro, C. Sue, D. Shungu, 2004, The Journal of pediatrics.

Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis

N. Bresolin, G. Comi, G. Scarlato, 1993, Journal of the Neurological Sciences.

Predictors of Long-Term Recurrent Vascular Events After Ischemic Stroke at Young Age: The Italian Project on Stroke in Young Adults

R. Calabró, A. Adami, L. Iacoviello, 2014, Circulation.

Clinical Pregenetic Screening for Stroke Monogenic Diseases: Results From Lombardia GENS Registry

G. Comi, S. Corti, E. Capitani, 2016, Stroke.

Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke

M. Silvestrini, E. Beghi, F. Orzi, 2016, Journal of Neuroinflammation.

Subclinical Vascular Brain Lesions in Young Adults With Acute Ischemic Stroke

A. Padovani, M. Zedde, R. Pascarella, 2021, Stroke.

Muscle mitochondria investigation in myotonic dystrophy.

N. Bresolin, G. Vita, A. Toscano, 1993, European neurology.

Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level

G. Comi, M. Zeviani, G. Scarlato, 1994, Acta Neuropathologica.

Efficiency in stroke management from acute care to rehabilitation: bedside versus telemedicine consultation.

F. Molteni, C. Giovanzana, Giovanni Cannaviello, 2019, European journal of physical and rehabilitation medicine.

The Italian Project on Stroke in Young Adults Predictors of Long-Term Recurrent Vascular Events After Ischemic Stroke at Young Age:

R. Calabró, A. Adami, L. Iacoviello, 2014 .

on behalf of the Italian Project on Stroke in Young Adults (IPSYS) Investigators

R. Calabró, A. Adami, L. Iacoviello, 2014 .

Connective tissue anomalies in patients with spontaneous cervical artery dissection

A. Padovani, A. Pezzini, A. Morotti, 2014, Neurology.

Anionic phospholipids calcium binding sites in Duchenne and murine X‐linked muscular dystrophy

G. Scarlato, M. Moggio, A. Prelle, 1994, Muscle & nerve.

Predictors of Long-Term Recurrent Vascular Events After Ischemic Stroke at Young Age The Italian Project on Stroke in Young Adults

R. Calabró, A. Adami, D. Bonifati, 2014 .

Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease: consensus recommendations.

Arslanian, P. Kaplan, J. Charrow, 2004, The Journal of pediatrics.