Caterina Tonon

Incidence and short-term prognosis of status epilepticus in adults in Bologna, Italy.

Proton magnetic resonance spectroscopy study of brain metabolism in obstructive sleep apnoea syndrome before and after continuous positive airway pressure treatment.

Prostate cancer: sextant localization with MR imaging, MR spectroscopy, and 11C-choline PET/CT.

Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease.

Atherosclerotic aortic lesions increase the risk of cerebral embolism during carotid stenting in patients with complex aortic arch anatomy.

Distribution of neurochemical abnormalities in patients with narcolepsy with cataplexy: An in vivo brain proton MR spectroscopy study.

Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.

A combined a-EEG and MR spectroscopy study in term newborns with hypoxic-ischemic encephalopathy.

Cerebral functions and metabolism after antegrade selective cerebral perfusion in aortic arch surgery.

A new case of idiopathic hemiplegia hemiconvulsion syndrome.

Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations.

Accuracy of MRI/MRSI-based transrectal ultrasound biopsy in peripheral and transition zones of the prostate gland in patients with prior negative biopsy.

A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.

Brain diffusion-weighted imaging in Friedreich's ataxia.

Magnetic resonance imaging and spectroscopy in the evaluation of neuromuscular disorders and fatigue.

Abnormal medial thalamic metabolism in patients with idiopathic restless legs syndrome.

Secondary post-geniculate involvement in Leber's hereditary optic neuropathy.

Low brain iron content in idiopathic restless legs syndrome patients detected by phase imaging.

Imaging brain functional and metabolic changes in restless legs syndrome.

Inflammatory mediators and cerebral embolism in carotid stenting: new markers of risk.

Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1.

Narcolepsy is a common phenotype in HSAN IE and ADCA-DN.

'Behr syndrome' with OPA1 compound heterozygote mutations.

Syndromic parkinsonism and dementia associated with OPA1 missense mutations.

Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.

The contribution of cerebellar proton magnetic resonance spectroscopy in the differential diagnosis among parkinsonian syndromes.

Brain magnetic resonance metabolic and microstructural changes in adult-onset autosomal dominant leukodystrophy.

The association between restless legs syndrome, cardiovascular and metabolic diseases: hypotheses and evidence from the literature.

A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings.

Combined Cerebellar Proton MR Spectroscopy and DWI Study of Patients with Friedreich's Ataxia.

ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy.

Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1.

Accuracy of MR markers for differentiating Progressive Supranuclear Palsy from Parkinson's disease.

Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy.

Voxel-based morphometry to detect effect of APOE on brain gray matter changes in Parkinson's Disease.

Magnetic Resonance Parkinsonism Index: diagnostic accuracy of a fully automated algorithm in comparison with the manual measurement in a large Italian multicentre study in patients with progressive supranuclear palsy.

Brain structural profile of multiple system atrophy patients with cognitive impairment.

The effect of diffusion gradient direction number on corticospinal tractography in the human brain: an along-tract analysis.

White matter and cortical changes in atypical parkinsonisms: A multimodal quantitative MR study.

Proton MR Spectroscopy in Patients With Sleep-Related Hypermotor Epilepsy (SHE): Evidence of Altered Cingulate Cortex Metabolism.

Multi-class parkinsonian disorders classification with quantitative MR markers and graph-based features using support vector machines.

Mitochondrial dysfunction in myotonic dystrophy type 1.

Brain functional connectivity in sleep-related hypermotor epilepsy.

Cognitive Rehabilitation and Transcranial Direct Current Stimulation in a Patient with Posterior Cortical Atrophy: An fMRI Study.

Along-tract analysis of the arcuate fasciculus using the Laplacian operator to evaluate different tractography methods.

Stridor-related gray matter alterations in multiple system atrophy: A pilot study.

Effects of Light Treatment on Sleep, Cognition, Mood, and Behavior in Alzheimer's Disease: A Systematic Review.

Predicting conversion from mild cognitive impairment to Alzheimer's disease using brain H-MRS and volumetric changes: A two- year retrospective follow-up study.

L-Dopa Modulation of Brain Connectivity in Parkinson's Disease Patients: A Pilot EEG-fMRI Study.

Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications.

An Evolutionary Cancer Epigenetic Approach Revealed DNA Hypermethylation of Ultra-Conserved Non-Coding Elements in Squamous Cell Carcinoma of Different Mammalian Species.

Intravenous immunoglobulin therapy in COVID-19-related encephalopathy.

''Eye of tiger sign" mimic in patients with spastic paraplegia gene 7 (SPG7) mutations.

Major cerebral vessels involvement in patients with MELAS syndrome: Worth a scan? A systematic review.

From Neurosurgical Planning to Histopathological Brain Tumor Characterization: Potentialities of Arcuate Fasciculus Along-Tract Diffusion Tensor Imaging Tractography Measures.

Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations.

Author response to the letter regarding the publication titled "Major cerebral vessels involvement in patients with MELAS syndrome: worth a scan? A systematic review".

The Combination of Metabolic Posterior Cingulate Cortical Abnormalities and Structural Asymmetries Improves the Differential Diagnosis Between Primary Progressive Aphasia and Alzheimer's Disease.