about
Magnetic resonance spectroscopy in the evaluation of treatment efficacy in unipolar major depressive disorder: a review of the literatureCongenital muscular dystrophies with defective glycosylation of dystroglycan: a population studySpectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutationsNerve Fascicles and Epineurium Volume Segmentation of Peripheral Nerve Using Magnetic Resonance Micro-neurography.Complications in major depressive disorder therapy: a review of magnetic resonance spectroscopy studies.Multiple sclerosis: hyperintense dentate nucleus on unenhanced T1-weighted MR images is associated with the secondary progressive subtype.MR Micro-Neurography and a Segmentation Protocol Applied to Diabetic Neuropathy.In Vivo MR Microneurography of the Tibial and Common Peroneal Nerves.DTI and MR Volumetry of Hippocampus-PC/PCC Circuit: In Search of Early Micro- and Macrostructural Signs of Alzheimers's Disease.A chaperone enhances blood α-glucosidase activity in Pompe disease patients treated with enzyme replacement therapy.ICHD-II diagnostic criteria for Tolosa-Hunt syndrome in idiopathic inflammatory syndromes of the orbit and/or the cavernous sinus.What insights have new imaging techniques given into aggressive forms of MS--different forms of MS or different from MS?Late-onset Pompe disease: a genetic-radiological correlation on cerebral vascular anomalies.Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment.Air pollution is associated to the multiple sclerosis inflammatory activity as measured by brain MRI.POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study.Predictors of outcome in a large retrospective cohort of patients with transverse myelitis.User interface of a teleradiology system for the MR assessment of multiple sclerosis.Good outcome in adult-onset Rasmussen's encephalitis syndrome: is recovery possible?Advanced magnetic resonance imaging in benign hereditary chorea: study of two familial cases.Novel hypomyelinating leukoencephalopathy affecting early myelinating structures: clinical course in two brothers.Limbic hyperconnectivity in the vegetative state.Congenital muscular dystrophies with cognitive impairment. A population study.Effectiveness of intravenous immunoglobulin treatment in adult patients with steroid-resistant monophasic or recurrent acute disseminated encephalomyelitis.Postinfectious neurologic syndromes: a prospective cohort study.Parahippocampal Involvement in Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis: A Proof of Concept from Memory-Guided Saccades.Bing-Neel Syndrome: Illustrative Cases and Comprehensive Review of the Literature.Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.MRI in sarcoglycanopathies: a large international cohort study.Do MRI Structured Reports for Multiple Sclerosis Contain Adequate Information for Clinical Decision Making?COL4A1-related disease: raised creatine kinase and cerebral calcification as useful pointers.Muscle MRI of classic infantile pompe patients: Fatty substitution and edema-like changes.Early-onset movement disorder as diagnostic marker in genetic syndromes: Three cases of FOXG1-related syndrome.Efficacy of rituximab as third-line therapy in combined central and peripheral demyelination."Acquired" Dandy-Walker malformation and cerebellar hemorrhage: Usefulness of serial MRI.Bilateral trigeminal enhancement on magnetic resonance imaging in a patient with multiple sclerosis and trigeminal neuralgia.MR peri-CSF lesions and CSF oligoclonal bands in Italian multiple sclerosis patients.Cerebellum enlargement and corpus callosum agenesis: a longitudinal case report.New molecular findings in congenital myopathies due to selenoprotein N gene mutations.Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength response.
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