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Manuela Napoli

Showing results (31-40 of 59) with videos related to

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Genes|June 27, 2024
RNF213 Polymorphisms in Intracranial Artery DissectionMarialuisa Zedde, Ilaria Grisendi, Federica Assenza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 9, 2024
Cerebellar mutism syndrome caused by bilateral cerebellar hemorrhage in adults: a case report and review of the literatureMarialuisa Zedde, Ilaria Grisendi, Federica Assenza, et al.
BMC Neurology|October 22, 2020
Extracranial metastases in secondary glioblastoma multiforme: a case reportJessica Rossi, Lucia Giaccherini, Francesco Cavallieri, et al.
Journal of Clinical Medicine|July 13, 2024
Neurovascular Issues in Antiphospholipid Syndrome: Arterial Vasculopathy from Small to Large Vessels in a Neuroradiological PerspectiveMarialuisa Zedde, Ilaria Grisendi, Federica Assenza, et al.
Neurology. Clinical Practice|December 28, 2023
Vestibular Hypofunction in ARSACS Syndrome: A Possible Pitfall in the Differential Diagnosis of Recessive Cerebellar and Afferent AtaxiasGiacomo Argenziano, Francesco Cavallieri, Andrea Castellucci, et al.
Frontiers in Oncology|January 23, 2023
Case Report: Pituitary metastasis as a presenting manifestation of silent gastric cardia adenocarcinomaAndrea Ghezzi, Jessica Rossi, Francesco Cavallieri, et al.
American Journal of Medical Genetics. Part A|September 5, 2024
Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literatureChiara Brugnoli, Susanna Rizzi, Carlo Alberto Cesaroni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 18, 2024
Obsessive-compulsive disorder as a first manifestation of Ataxia with Oculomotor Apraxia type 2 due to a novel mutation of SETX geneFederica Galota, Giulia Di Rauso, Francesca Sireci, et al.
BMC Ophthalmology|June 1, 2013
Unilateral proptosis in thyroid eye disease with subsequent contralateral involvement: retrospective follow-up studyDiego Strianese, Raffaele Piscopo, Andrea Elefante, et al.
Cancers|October 14, 2022
Safety of Inhomogeneous Dose Distribution IMRT for High-Grade Glioma Reirradiation: A Prospective Phase I/II Trial (GLIORAD TRIAL)Patrizia Ciammella, Salvatore Cozzi, Andrea Botti, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

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Pageof 6
Genes|June 27, 2024
RNF213 Polymorphisms in Intracranial Artery DissectionMarialuisa Zedde, Ilaria Grisendi, Federica Assenza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 9, 2024
Cerebellar mutism syndrome caused by bilateral cerebellar hemorrhage in adults: a case report and review of the literatureMarialuisa Zedde, Ilaria Grisendi, Federica Assenza, et al.
BMC Neurology|October 22, 2020
Extracranial metastases in secondary glioblastoma multiforme: a case reportJessica Rossi, Lucia Giaccherini, Francesco Cavallieri, et al.
Journal of Clinical Medicine|July 13, 2024
Neurovascular Issues in Antiphospholipid Syndrome: Arterial Vasculopathy from Small to Large Vessels in a Neuroradiological PerspectiveMarialuisa Zedde, Ilaria Grisendi, Federica Assenza, et al.
Neurology. Clinical Practice|December 28, 2023
Vestibular Hypofunction in ARSACS Syndrome: A Possible Pitfall in the Differential Diagnosis of Recessive Cerebellar and Afferent AtaxiasGiacomo Argenziano, Francesco Cavallieri, Andrea Castellucci, et al.
Frontiers in Oncology|January 23, 2023
Case Report: Pituitary metastasis as a presenting manifestation of silent gastric cardia adenocarcinomaAndrea Ghezzi, Jessica Rossi, Francesco Cavallieri, et al.
American Journal of Medical Genetics. Part A|September 5, 2024
Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literatureChiara Brugnoli, Susanna Rizzi, Carlo Alberto Cesaroni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 18, 2024
Obsessive-compulsive disorder as a first manifestation of Ataxia with Oculomotor Apraxia type 2 due to a novel mutation of SETX geneFederica Galota, Giulia Di Rauso, Francesca Sireci, et al.
BMC Ophthalmology|June 1, 2013
Unilateral proptosis in thyroid eye disease with subsequent contralateral involvement: retrospective follow-up studyDiego Strianese, Raffaele Piscopo, Andrea Elefante, et al.
Cancers|October 14, 2022
Safety of Inhomogeneous Dose Distribution IMRT for High-Grade Glioma Reirradiation: A Prospective Phase I/II Trial (GLIORAD TRIAL)Patrizia Ciammella, Salvatore Cozzi, Andrea Botti, et al.
Pageof 6