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39 results on '"DI IORIO, Giuseppe"'

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1. Diffuse glioblastoma resembling acute hemorrhagic leukoencephalitis

2. Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study

3. Late adult-onset adrenomyeloneuropathy evolving with atypical severe frontal lobe syndrome: Importance of neuroimaging

4. Adult‐onset brain tumors and neurodegeneration: Are polyphenols protective?

5. Successful long-term therapy with flecainide in a family with paramyotonia congenita

6. Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease

7. Fingolimod reduces the clinical expression of active demyelinating lesions in MS

8. Synergistic interplay between curcumin and polyphenol-rich foods in the mediterranean diet: Therapeutic prospects for neurofibromatosis 1 patients

9. The level of 24-Hydroxycholesteryl Esters is an Early Marker of Alzheimer's Disease

10. Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease

11. Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection

12. Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study

13. The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients

14. Lymphocytosis as a response biomarker of natalizumab therapeutic efficacy in multiple sclerosis

15. LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population

16. Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

17. Peripheral neuropathy in hepatitis-related mixed cryoglobulinemia: Electrophysiologic follow-up study

18. Increased Cerebrospinal Fluid Levels of 3,3′,5′-Triiodothyronine in Patients with Alzheimer’s Disease

19. The influence of illness-related variables, personal resources and context-related factors on real-life functioning of people with schizophrenia

20. A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy

21. Clinical genetic analysis of Parkinson's disease in the contursi kindred

22. Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years

23. New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy

24. Viral RNA in nerve tissues of patients with hepatitis C infection and peripheral neuropathy

25. Autonomic neuropathy in mixed cryoglobulinemia

26. [Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia]

27. Long-term treatment with interferon-beta therapy for multiple sclerosis and occurrence of Graves' disease

28. Relative sparing of extraocular muscles in myotonic dystrophy: an electrooculographic study

29. A comment on: 'Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy' by Paola Strocchi et al., FEBS Letters 359 (1995) 203-205

30. Familial amyloidotic polyneuropathy: description of an Italian kindred

31. A case of diffuse lupus encephalopathy successfully treated with high-dose intravenous methylprednisolone

32. Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome

33. A large kindred with autosomal dominant Parkinson's disease

34. Neurophysiological alterations in cryoglobulinemia: a study of 10 patients

35. Sanfilippo B syndrome (MPS III B): Case report with analysis of CSF mucopolysaccharides and conjunctival biopsy

36. Supratentorial hemangioblastoma in a child. Case report

37. Pathogenesis and prevention of central pontine myelinolysis: a case report

38. Behçet's disease: an unusual case with bilateral obliterating retinal panarteritis and ischemic optic atrophy

39. Histopathological heterogeneity and cytopathological similarity of findings in different muscles of two brothers affected by rigid spine syndrome

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