Bibliografia

ELENCO DELLE PUBBLICAZIONI del Gruppo multidisciplinare per l’assistenza ai malati di SLA e per la ricerca sulla SLA (ALS Care & Research Group, ALSCaReG) P. Bongioanni “La terapia farmacologica e gli attuali trial clinici” Atti del Convegno “Vivere con la

1. Introduction Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the progressive loss of the motor neurons leading to muscle weakness, increasing disability and death of affected individuals. Several pathogenic hypotheses have been proposed to explain the selective

Abstract. Amyotrophic lateral sclerosis (ALS) is the most common degenerative motor neuron disease in adults, and dysphagia is one of its most frequent and disabling symptoms. Oropharyngoesophageal scintigraphy (OPES) permits a functional and semiquantitative study of the various stages of

Amyotrophic lateral sclerosis (ALS) is the most common motor neurone disorder in human adults. It is characterized by selective and progressive degeneration of upper and lower motor neurones in the spinal cord, brain stem and motor cortex. Clinically this process