P. Scoppettuolo

发表

Neurological involvement in SARS-CoV-2 infection: A clinical systematic review

S. Borrelli, G. Naeije, P. Scoppettuolo, 2020, Brain, Behavior, & Immunity - Health.

THE EUROPEAN/INTERNATIONAL FIBROMUSCULAR DYSPLASIA REGISTRY AND INITIATIVE (FEIRI)- CLINICAL PHENOTYPES AND THEIR PREDICTORS BASED ON A COHORT OF ONE THOUSAND PATIENTS.

R. Cianci, P. Salice, J. Segura, 2020, Cardiovascular research.

Headache, Bilateral Carotid Stenosis, and Hypoglossal Palsy Revealing Granulomatosis with Polyangiitis: An Innovative Application of Vessel-Wall MRI

S. Goldman, G. Naeije, N. Ligot, 2020, Journal of clinical neurology.

MS diagnosis in a male patient with m.11778G > A Leber’s hereditary optic neuropathy

Audrey Meunier, C. Retif, P. Scoppettuolo, 2022, Neurological Sciences.

Clinical use of frataxin measurement in a patient with a novel deletion in the FXN gene

G. De Michele, A. Filla, A. Tessa, 2013, Journal of Neurology.

Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.

N. Samani, L. Mazzolai, A. Maas, 2020, Circulation.

Epileptic activity in neurological deterioration after ischemic stroke, a continuous EEG study

C. Depondt, N. Gaspard, G. Naeije, 2019, Clinical Neurophysiology.

p.Gly743Val Mutation in COL4A1 Is Responsible for Familial Porencephaly and Severe Hypermetropia

P. van Bogaert, G. Naeije, N. Ligot, 2020, Frontiers in Neurology.

Utility of A2L2 score in acute ischemic stroke patient triage: the "H.uni" experience.

J. Raymackers, M. Rutgers, P. Scoppettuolo, 2024, Acta neurologica Belgica.