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pro vyhledávání: '"Ester Boniello"'
Autor:
Donato Lacedonia, Onofrio Resta, Felice Gadaleta, Pierluigi Carratù, Lucia Spicuzza, Anna Cassano, Ester Boniello, Giuseppe Di Maria, Cristina Scoditti, Mauro Maniscalco
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 4, Iss 1, p 10 (2009)
Orphanet Journal of Rare Diseases, Vol 4, Iss 1, p 10 (2009)
Background Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease, which rapidly leads to chronic respiratory failure requiring mechanical ventilation. Currently, forced vital capacity (FVC) < 50% is considered as physiologic marker for a