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