| TC1: Old and new problems in neuromuscular disorders | ||
| 08.30 – 10.30 | H. Lochmüller (UK): | Sporadic and congenital Myasthenia: how to diagnose and treat |
| W. King Engel (USA): | Diabetic and other dysimmune neuropathies: pathogenesis and treatment options | |
| 10.30 – 11.00 | Coffee break | |
| 11.00 – 13.00 | C. Angelini (Italy): | Metabolic Myopathies: new phenotypes and treatable conditions |
| F. Muntoni (UK): | Neuromuscular Disorders in infancy – What’s new about phenotypes and clinical trials | |
| TC2: Neuromuscular immunology for clinicians | ||
| 08.30 – 10.30 | M. Dalakas (UK): | Practical basic immunology for neuromuscular specialists, including evaluation of relevant therapeutic agents |
| E. Nobile-Orazio (Italy): | Peripheral Neuropathies an immunologic approach to diagnosis | |
| 10.30 – 11.00 | Coffee break | |
| 11.00 – 13.00 | F. Mastaglia (Australia): | Inflammatory Myopathies: Practical aspects of diagnosis and treatment |
| A. Vincent (UK): | Antibodies in Myasthenia: how to diagnose them | |
| TC3: Genetics for clinicians | ||
| 08.30- 10.30 | V. Nigro (Italy): | How important is a precise diagnosis for patients with muscular dystrophies and other myopathies |
| S. DiMauro (USA): | The quaint genetic behaviour in mitochondrial myopathies | |
| 10.30 - 11.00 | Coffee break | |
| 11.00 - 13.00 | G. Novelli (Italy): | Trinucleotide Repeat Disorders:the pathogenic basis of clinical manifestations. Possible therapeutic approaches |
| M. Reilly (UK): | Genetic Neuropathies – Is categorizing important? Treatment, now or in near-future? | |
| TC4: Clinical, histochemical and electrophysiologic approaches to neuromuscular diseases | ||
| 08.30 - 10.30 | Z. Argov (Israel): | Clinical clues in the diagnosis of adult hereditary myopathies |
| A. Oldfors (Sweden): | Histochemical and electron-microscopic approach to muscle diseases: slide sessions | |
| 10.30 - 11.00 | Coffee break | |
| 11.00 - 13.00 | L. Santoro (Italy): | Practical pearls from neurophysiologic experience with peripheral neuropathies |
| R. Baloh (USA): | The new inherited pathological basis of motor neuron disorders | |
| TC5: Diagnosis and management of acute neuromuscular disorders | ||
| 8.30- 10.30 | G. Said (France): | Acute peripheral nerve disorders |
| A. Evoli (Italy): | Management and treatment of myasthenic crisis | |
| 10.30 – 11.00 | Coffee break | |
| 11.00 – 13.00 | A. Toscano (Italy): | Rabdomyolysis: causes and possible therapies |
| M. Hanna (UK): | How to deal with sudden muscle weakness | |