Neuroradiology Unit
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Fetal development of the corpus callosum: Insights from a 3T DTI and tractography study in a patient with segmental callosal agenesis.
The neuroradiology journal Oct, 2016 | Pubmed ID: 27549148
Muscle MRI of classic infantile pompe patients: Fatty substitution and edema-like changes.
Muscle & nerve 06, 2017 | Pubmed ID: 27668838
Acute flaccid myelitis associated with enterovirus-D68 infection in an otherwise healthy child.
Virology journal 01, 2017 | Pubmed ID: 28081720
Gray matter volumes may predict the clinical response to paliperidone palmitate long-acting in acute psychosis: A pilot longitudinal neuroimaging study.
Psychiatry research. Neuroimaging Mar, 2017 | Pubmed ID: 28161644
Chronic recurrent multifocal osteomyelitis presenting with Tolosa-Hunt syndrome in a 13-year-old boy.
Clinical and experimental rheumatology May-Jun, 2017 | Pubmed ID: 28598320
X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.
Parkinsonism & related disorders Nov, 2017 | Pubmed ID: 28851564
From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth.
PloS one , 2018 | Pubmed ID: 29304146
Clinical safety of 3-T brain magnetic resonance imaging in newborns.
Pediatric radiology 07, 2018 | Pubmed ID: 29594440
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome.
American journal of medical genetics. Part A 06, 2018 | Pubmed ID: 29663667
Diffusion tensor imaging in the musculoskeletal and peripheral nerve systems: from experimental to clinical applications.
European radiology experimental , 2017 | Pubmed ID: 29708174
CSF β-amyloid predicts prognosis in patients with multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) 08, 2019 | Pubmed ID: 30084711
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature.
Frontiers in neurology , 2018 | Pubmed ID: 30116219
The Neuroanatomy of Somatoform Disorders: A Magnetic Resonance Imaging Study.
Psychosomatics May - Jun, 2019 | Pubmed ID: 30119840
Stormorken Syndrome Caused by a p.R304W Mutation: The First Italian Patient and a Review of the Literature.
Frontiers in neurology , 2018 | Pubmed ID: 30374325
Structural and metabolic cerebral alterations between elderly bipolar disorder and behavioural variant frontotemporal dementia: A combined MRI-PET study.
The Australian and New Zealand journal of psychiatry 05, 2019 | Pubmed ID: 30545239
Value of structured reporting in neuromuscular disorders.
La Radiologia medica Jul, 2019 | Pubmed ID: 30852791
Immune-mediated necrotizing myopathy due to statins exposure.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology Dec, 2018 | Pubmed ID: 30944904
Early Magnetic Resonance Imaging for Patients With Idiopathic Sudden Sensorineural Hearing Loss in an Emergency Setting.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 10, 2019 | Pubmed ID: 31498290
Minimally invasive fetal surgery for myelomeningocele: preliminary report from a single center.
Neurosurgical focus 10, 2019 | Pubmed ID: 31574466
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients.
Journal of neurology Apr, 2020 | Pubmed ID: 31776722
Prenatal magnetic resonance imaging within the 26th week of gestation may predict the fate of isolated upward rotation of the cerebellar vermis: insights from a multicentre study.
European radiology Apr, 2020 | Pubmed ID: 31900695
A case series of CHARGE syndrome: identification of key features for a neonatal diagnosis.
Italian journal of pediatrics Apr, 2020 | Pubmed ID: 32326958
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency.
Annals of clinical and translational neurology 05, 2020 | Pubmed ID: 32329585
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form.
Molecular genetics & genomic medicine Jun, 2020 | Pubmed ID: 32578970
Effects of Early Intervention on Visual Function in Preterm Infants: A Randomized Controlled Trial.
Frontiers in pediatrics , 2020 | Pubmed ID: 32582595
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society Jul, 2020 | Pubmed ID: 32800423
Giuseppe Delvecchio*,1,
Lucio Oldani*,2,
Gian Mario Mandolini2,
Alessandro Pigoni3,
Valentina Ciappolino2,
Giandomenico Schiena2,
Matteo Lazzaretti2,
Elisabetta Caletti2,
Viviana Barbieri1,
Claudia Cinnante4,
Fabio Triulzi1,4,
Paolo Brambilla1,2
1Department of Pathophysiology and Transplantation, University of Milan,
2Department of Neurosciences and Mental Health, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico,
3MoMiLab Research Unit, IMT School for Advanced Studies Lucca,
4Neuroradiology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
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