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MRI/MRS in neuroinflammation: methodology and applicationsMutation in the SYNJ1 gene associated with autosomal recessive, early-onset ParkinsonismChanges in magnetic resonance imaging disease measures over 3 years in mildly disabled patients with relapsing-remitting multiple sclerosis receiving interferon β-1a in the COGnitive Impairment in MUltiple Sclerosis (COGIMUS) studyA voxel-based morphometry study of disease severity correlates in relapsing-- remitting multiple sclerosis.Intracranial pressure in unresponsive chronic migraineReduced prefrontal activity predicts exaggerated striatal dopaminergic function in schizophrenia.Abnormal or delayed development of the posterior membranous area of the brain: anatomy, ultrasound diagnosis, natural history and outcome of Blake's pouch cyst in the fetus.Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variabilityDefault-mode network changes in Huntington's disease: an integrated MRI study of functional connectivity and morphometry.Is uterine artery embolization for cervical ectopic pregnancy always safe?Patterns of structural MRI abnormalities in deficit and nondeficit schizophrenia.Effects of Bacille Calmette-Guerin after the first demyelinating event in the CNSImmunometabolic profiling of patients with multiple sclerosis identifies new biomarkers to predict disease activity during treatment with interferon beta-1a.Is advanced neuroimaging for neuroradiologists? A systematic review of the scientific literature of the last decade.Alterations of functional connectivity of the motor cortex in Fabry disease: An RS-fMRI study.Relationship between simultaneously acquired resting-state regional cerebral glucose metabolism and functional MRI: a PET/MR hybrid scanner study.Growth hormone/IGF-1 axis longitudinal evaluation in clinically isolated syndrome patients on interferon β-1b therapy: stimulation tests and correlations with clinical and radiological conversion to multiple sclerosis.Cerebral Involvement in Stargardt's Disease: A VBM and TBSS Study.Modifications of resting state networks in spinocerebellar ataxia type 2.A Voxel-Based Approach to Explore Local Dose Differences Associated With Radiation-Induced Lung Damage.SPECT imaging of GABA(A)/benzodiazepine receptors and cerebral perfusion in mild cognitive impairment.Atorvastatin combined to interferon to verify the efficacy (ACTIVE) in relapsing-remitting active multiple sclerosis patients: a longitudinal controlled trial of combination therapy.Is the distance between mammillary bodies predictive of a thickened third ventricle floor?[Cancer of the pancreas and the periampullar region: usefulness of tumor markers produced with the monoclonal antibody technique]Complex phenotype in an Italian family with a novel mutation in SPG3A.Extra-osseous 99mTc methylene diphosphonate uptake detected enlargement of the knee joint in patient with polyarthritis.Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task.18F-FDG PET/CT, 99mTc-MIBI, and MRI in evaluation of patients with multiple myeloma.Default mode network modifications in Fabry disease: A resting-state fMRI study with structural correlations.Avolition-Apathy and White Matter Connectivity in Schizophrenia: Reduced Fractional Anisotropy Between Amygdala and Insular Cortex.Altered functional connectivity of interoception in illness anxiety disorder.Prenatal 2D and 3D ultrasound diagnosis of diprosopus: case report with post-mortem magnetic resonance images (MRI) and review of the literature.Natalizumab is effective in multiple sclerosis patients switching from other disease modifying therapies in clinical practice.Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study.Correlation between fatigue and brain atrophy and lesion load in multiple sclerosis patients independent of disability.MRI detects acute degeneration of the nigrostriatal dopamine system after MPTP exposure in hemiparkinsonian monkeys.In vivo dentate nucleus MRI relaxometry correlates with previous administration of Gadolinium-based contrast agents.CCM3/PDCD10 gene mutation in cerebral cavernous malformations associated with hyperkeratotic cutaneous capillary venous malformations.Grey:white matter ratio at diagnosis and the risk of 10-year multiple sclerosis progression.Functional MRI signal fluctuations highlight altered resting brain activity in Huntington's disease.
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description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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Mario Quarantelli
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P1153
7004524756
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P2456
P31
P496
0000-0001-7836-454X