Claudia Cinnante

Fetal development of the corpus callosum: Insights from a 3T DTI and tractography study in a patient with segmental callosal agenesis.

Muscle MRI of classic infantile pompe patients: Fatty substitution and edema-like changes.

Acute flaccid myelitis associated with enterovirus-D68 infection in an otherwise healthy child.

Gray matter volumes may predict the clinical response to paliperidone palmitate long-acting in acute psychosis: A pilot longitudinal neuroimaging study.

Chronic recurrent multifocal osteomyelitis presenting with Tolosa-Hunt syndrome in a 13-year-old boy.

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.

From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth.

Clinical safety of 3-T brain magnetic resonance imaging in newborns.

A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome.

Diffusion tensor imaging in the musculoskeletal and peripheral nerve systems: from experimental to clinical applications.

CSF β-amyloid predicts prognosis in patients with multiple sclerosis.

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature.

The Neuroanatomy of Somatoform Disorders: A Magnetic Resonance Imaging Study.

Stormorken Syndrome Caused by a p.R304W Mutation: The First Italian Patient and a Review of the Literature.

Structural and metabolic cerebral alterations between elderly bipolar disorder and behavioural variant frontotemporal dementia: A combined MRI-PET study.

Value of structured reporting in neuromuscular disorders.

Immune-mediated necrotizing myopathy due to statins exposure.

Early Magnetic Resonance Imaging for Patients With Idiopathic Sudden Sensorineural Hearing Loss in an Emergency Setting.

Minimally invasive fetal surgery for myelomeningocele: preliminary report from a single center.

MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients.

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.

A case series of CHARGE syndrome: identification of key features for a neonatal diagnosis.

Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency.

MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form.

Effects of Early Intervention on Visual Function in Preterm Infants: A Randomized Controlled Trial.

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.