Claudia Cinnante

Neuroradiology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Affiliated withFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 3	2020

Other Publications

Article	Year
Fetal development of the corpus callosum: Insights from a 3T DTI and tractography study in a patient with segmental callosal agenesis. The neuroradiology journal\| PubMed ID: 27549148	2016
Muscle MRI of classic infantile pompe patients: Fatty substitution and edema-like changes. Muscle & nerve\| PubMed ID: 27668838	2017
Acute flaccid myelitis associated with enterovirus-D68 infection in an otherwise healthy child. Virology journal\| PubMed ID: 28081720	2017
Gray matter volumes may predict the clinical response to paliperidone palmitate long-acting in acute psychosis: A pilot longitudinal neuroimaging study. Psychiatry research. Neuroimaging\| PubMed ID: 28161644	2017
Chronic recurrent multifocal osteomyelitis presenting with Tolosa-Hunt syndrome in a 13-year-old boy. Clinical and experimental rheumatology\| PubMed ID: 28598320	2017
X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene. Parkinsonism & related disorders\| PubMed ID: 28851564	2017
From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth. PloS one\| PubMed ID: 29304146	2018
Clinical safety of 3-T brain magnetic resonance imaging in newborns. Pediatric radiology\| PubMed ID: 29594440	2018
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome. American journal of medical genetics. Part A\| PubMed ID: 29663667	2018
Diffusion tensor imaging in the musculoskeletal and peripheral nerve systems: from experimental to clinical applications. European radiology experimental\| PubMed ID: 29708174	2017
CSF β-amyloid predicts prognosis in patients with multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England)\| PubMed ID: 30084711	2019
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\| PubMed ID: 30116219	2018
The Neuroanatomy of Somatoform Disorders: A Magnetic Resonance Imaging Study. Psychosomatics\| PubMed ID: 30119840	2019
Stormorken Syndrome Caused by a p.R304W Mutation: The First Italian Patient and a Review of the Literature. Frontiers in neurology\| PubMed ID: 30374325	2018
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\| PubMed ID: 30545239	2019
Value of structured reporting in neuromuscular disorders. La Radiologia medica\| PubMed ID: 30852791	2019
Immune-mediated necrotizing myopathy due to statins exposure. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology\| PubMed ID: 30944904	2018
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\| PubMed ID: 31498290	2019
Minimally invasive fetal surgery for myelomeningocele: preliminary report from a single center. Neurosurgical focus\| PubMed ID: 31574466	2019
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients. Journal of neurology\| PubMed ID: 31776722	2020
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\| PubMed ID: 31900695	2020
A case series of CHARGE syndrome: identification of key features for a neonatal diagnosis. Italian journal of pediatrics\| PubMed ID: 32326958	2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency. Annals of clinical and translational neurology\| PubMed ID: 32329585	2020
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form. Molecular genetics & genomic medicine\| PubMed ID: 32578970	2020
Effects of Early Intervention on Visual Function in Preterm Infants: A Randomized Controlled Trial. Frontiers in pediatrics\| PubMed ID: 32582595	2020
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\| PubMed ID: 32800423	2020