Untitled Document
Nosography of neuromuscular
diseases in the light of recent acquisitions in molecular genetics; metabolic
myopathies general aspects and clinical approach; clinical heterogeneity of respiratory
chain enzyme defects; congenital muscular dystrophies; dystrophinopathies; congenital
myopathies; myotonic syndromes; hereditary motor and sensory neuropathy (HMSN)
and tomaculous neuropathy (HNPP); spinal muscle atrophies; diseases of neuromuscular
junction; current concepts review on the orthopaedic treatment of muscular diseases
of childhood; therapy of scoliosis in neuromuscular pathology; assisted ventilation;
home mechanical ventilation in neuromuscular diseases the example of the Duchenne
muscular dystrophy; prevention genetic counselling; prenatal diagnosis.
