144 results on '"Amato, Anthony"'
Search Results
2. A protocol to develop clinical guidelines for inclusion‐body myositis
3. Nuclear localization of valosin‐containing protein in normal muscle and muscle affected by inclusion‐body myositis
4. Frequency and Type of Cancers in Myotonic Dystrophy. A Retrospective Cross‐Sectional Study
5. Safety and outcomes of eculizumab for acetylcholine receptor‐positive generalized myasthenia gravis in clinical practice
6. Randomized phase 2 study of ACE‐083, a muscle‐promoting agent, in facioscapulohumeral muscular dystrophy
7. Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine
8. Lambert-eaton myasthenic syndrome and merkel cell carcinoma
9. Design of a randomized, double-blind, placebo-controlled Phase 2 clinical trial of the Toll-like receptor antagonist IMO-8400 in patients with dermatomyositis: 27
10. Retrospective analysis of safety and outcomes of rituximab for myasthenia gravis in patients ≥ 65 years old
11. Stiff person syndrome and rituximab
12. Medical costs and health-care resource use in patients with inflammatory myopathies in an insured population
13. A quantitative measure of handgrip myotonia in non-dystrophic myotonia
14. EPIDEMIOLOGY OF ADULT IDIOPATHIC INFLAMMATORY MYOPATHIES IN A U.S. MANAGED CARE PLAN
15. AANEM POSITION STATEMENT ON NEUROMUSCULAR MEDICINE QUALIFICATIONS
16. AN INTERACTIVE VOICE RESPONSE DIARY FOR PATIENTS WITH NON-DYSTROPHIC MYOTONIA
17. Permissive environment for B-cell maturation in myositis muscle in the absence of B-cell follicles
18. CLINICAL FINDINGS IN MUSK-ANTIBODY POSITIVE MYASTHENIA GRAVIS: A U.S. EXPERIENCE
19. SPORADIC LATE ONSET NEMALINE MYOPATHY RESPONSIVE TO IVIG AND IMMUNOTHERAPY
20. IMMUNE-MEDIATED NECROTIZING MYOPATHY ASSOCIATED WITH STATINS
21. DERMATOMYOSITIS-LIKE MUSCLE PATHOLOGY IN PATIENTS WITH CHRONIC GRAFT-VERSUS-HOST DISEASE
22. NATURE OF “TAU” IMMUNOREACTIVITY IN NORMAL MYONUCLEI AND INCLUSION BODY MYOSITIS
23. SARCOPLASMIC REDISTRIBUTION OF NUCLEAR TDP-43 IN INCLUSION BODY MYOSITIS
24. FAST-TWITCH SARCOMERIC AND GLYCOLYTIC ENZYME PROTEIN LOSS IN INCLUSION BODY MYOSITIS
25. Single muscle fiber contractile properties in adults with muscular dystrophy treated with MYO-029
26. MUSCLE-SPECIFIC KINASE (MUSK) ANTIBODY-ASSOCIATED MYASTHENIA GRAVIS AFTER BONE MARROW TRANSPLANTATION
27. MYELOID DENDRITIC CELLS IN INCLUSION-BODY MYOSITIS AND POLYMYOSITIS
28. NUCLEAR MEMBRANE PROTEINS ARE PRESENT WITHIN RIMMED VACUOLES IN INCLUSION-BODY MYOSITIS
29. Retrospective analysis of safety and outcomes of rituximab for myasthenia gravis in patients ≥65 years old.
30. Investigation of the psychometric properties of the inclusion body myositis functional rating scale with rasch analysis
31. Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine
32. Lambert-eaton myasthenic syndrome and merkel cell carcinoma
33. Lisa S. Krivackas
34. Immune‐mediated necrotizing myopathy associated with statins
35. Sporadic late onset nemaline myopathy responsive to IVIg and immunotherapy
36. Single muscle fiber contractile properties in adults with muscular dystrophy treated with MYO‐029
37. Myeloid dendritic cells in inclusion‐body myositis and polymyositis
38. Transthyretin amyloidosis presenting with multifocal demyelinating mononeuropathies
39. Late‐onset distal muscular dystrophy affecting the posterior calves
40. Randomized, controlled trial of intravenous immunoglobulin in myasthenia gravis
41. Clinical spectrum of chronic acquired demyelinating polyneuropathies
42. Clinical and genetic aspects of distal myopathies
43. Inflammatory myopathy associated with mixed connective tissue disease and scleroderma renal crisis
44. Cervicobrachial involvement in diabetic radiculoplexopathy
45. Multifocal acquired demyelinating sensory and motor neuropathy: The Lewis-Sumner syndrome
46. Chronic relapsing brachial plexus neuropathy with persistent conduction block
47. Isolated vitamin E deficiency
48. Hereditary neuropathy with liability to pressure palsies: Association with central nervous system demyelination
49. Tomaculous neuropathy: A clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p<11.2
50. Childhood‐onset oculopharyngodistal myopathy with chronic intestinal pseudo‐obstruction
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