477 results on '"Di Iorio, Giuseppe"'
Search Results
2. Disrupted relationship between “resting state” connectivity and task-evoked activity during social perception in schizophrenia
3. Fingolimod reduces the clinical expression of active demyelinating lesions in MS
4. First study on the peptidergic innervation of the brain superior sagittal sinus in humans
5. One novel GRN null mutation, two different aphasia phenotypes
6. Upcoming tactile events and body ownership in schizophrenia
7. Efficacy and Safety of Atypical Antipsychotics in Bipolar Disorder With Comorbid Substance Dependence: A Systematic Review
8. Mutation in the α-Synuclein Gene Indentified in Families with Parkinson's Disease
9. Alexithymia, suicide risk and serum lipid levels among adult outpatients with panic disorder
10. Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23
11. A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations
12. A novel diagnostic method to detect truncated neurofibromin in neurofibromatosis 1
13. Dipendenza da sesso
14. Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement
15. Novel autophagic vacuolar myopathies: Phenotype and genotype features
16. Diffuse glioblastoma resembling acute hemorrhagic leukoencephalitis
17. Alexithymia and Suicide Ideation in a Sample of Patients with Binge Eating Disorder
18. ATTRv amyloidosis Italian Registry: clinical and epidemiological data
19. P32. Vacuolated pas-positive lymphocytes: a screening test for pompe disease and other autophagic myopathies
20. Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: Electrophysiologic follow-up study
21. Increased Cerebrospinal Fluid Levels of 3,3′,5′-Triiodothyronine in Patients with Alzheimer’s Disease
22. A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis
23. Abnormal Accumulation of tTGase Products in Muscle and Erythrocytes of Chorea-Acanthocytosis Patients
24. Late adult-onset adrenomyeloneuropathy evolving with atypical severe frontal lobe syndrome: Importance of neuroimaging
25. Early posterior vitreous detachment is associated with LAMA5 dominant mutation
26. Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
27. Novel VCP mutations expand the mutational spectrum of frontotemporal dementia
28. Neuro-Behçet’s disease presenting as an isolated progressive cognitive and behavioral syndrome
29. Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility
30. Mutation in the alpha-Synuclein Gene Identified in Families with Parkinson's Disease
31. The genetic basis of undiagnosed muscular dystrophies and myopathies
32. Efficacy of Memantine in Schizophrenic Patients: A Systematic Review
33. Symptomatic heterozygosity due to definite GAA mutations in late onset Pompe disease
34. Peripersonal space boundary in schizotypy and schizophrenia
35. Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease
36. Successful long-term therapy with flecainide in a family with paramyotonia congenita
37. Vacuolated PAS‐positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy
38. Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease
39. Diffuse glioblastoma resembling acute hemorrhagic leukoencephalitis
40. Early diagnosis and early treatmentin LOPD: when asymptomatic patients should be treated
41. A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1)
42. An atypical case of sporadic presenile dementia
43. Symptomatic heterozygosity due to definite GAA mutation in late onset Pompe disease
44. Intracranial calcifications, parkinsonism and metabolic myopathy in disorder of calcium metbolism
45. A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease. A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease
46. Parkinsonism and mitochondrial myopathy in a calcium metabolism syndrome
47. Adult‐onset brain tumors and neurodegeneration: Are polyphenols protective?
48. Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients
49. Bupropion Augmentation in a Case of Compulsive Buying Disorder
50. The level of 24-Hydroxycholesteryl Esters is an Early Marker of Alzheimer’s Disease
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