Il contributo riporta i risultati del progetto europeo BuRQoL sul carico economico-sociale e sulla qualità della vita dei pazienti affetti da una decina di malattie rare in nove Paesi. In questo paper si riportano i risultati e le evidenze emerse per la Distrofia Muscolare di Duchenn
Background: Duchenne Muscular Dystrophy (DMD) is a rapidly progressive, lethal neuromuscular disorde...
Abstract Background Duchenne Muscular Dystrophy (DMD) is a rapidly progressive, lethal neuromuscular...
The purpose of this study was to evaluate the quality of life (QoL) of patients with Duchenne muscul...
Il contributo riporta i risultati del progetto europeo BuRQoL sul carico economico-sociale e sulla q...
Objective: This systematic review aims to update the evidence on Duchenne muscular dystrophy (DMD) i...
Al abordar la temática sobre la afectación en la calidad de vida en pacientes con distrofia muscular...
Objective: The objective of this study was to estimate the total cost of illness and economic burden...
Our study aimed to determine the burden of illness in dystrophinopathy type Duchenne (DMD) and Becke...
This paper describes the psycho-social treatments received by 502 patients with MDs and their relati...
BACKGROUND: Promising genetic therapies are being investigated in facioscapulohumeral muscular dystr...
Duchenne muscular dystrophy (DMD) is a rare neuromuscular disease characterized by progressive muscl...
Part of the Epidemiology Commons, and the Pediatrics Commons This Dissertation/Thesis is brought to ...
Objective: To assess quality of life of adults with Duchenne muscular dystrophy in the Netherlands a...
Ve své bakalářské práci jsem se zaměřila na kvalitu života u nemocných s myopatií. V teoretické část...
This cost-of-illness analysis based on information from 921 patients in Italy is part of a Europe-wi...
Background: Duchenne Muscular Dystrophy (DMD) is a rapidly progressive, lethal neuromuscular disorde...
Abstract Background Duchenne Muscular Dystrophy (DMD) is a rapidly progressive, lethal neuromuscular...
The purpose of this study was to evaluate the quality of life (QoL) of patients with Duchenne muscul...
Il contributo riporta i risultati del progetto europeo BuRQoL sul carico economico-sociale e sulla q...
Objective: This systematic review aims to update the evidence on Duchenne muscular dystrophy (DMD) i...
Al abordar la temática sobre la afectación en la calidad de vida en pacientes con distrofia muscular...
Objective: The objective of this study was to estimate the total cost of illness and economic burden...
Our study aimed to determine the burden of illness in dystrophinopathy type Duchenne (DMD) and Becke...
This paper describes the psycho-social treatments received by 502 patients with MDs and their relati...
BACKGROUND: Promising genetic therapies are being investigated in facioscapulohumeral muscular dystr...
Duchenne muscular dystrophy (DMD) is a rare neuromuscular disease characterized by progressive muscl...
Part of the Epidemiology Commons, and the Pediatrics Commons This Dissertation/Thesis is brought to ...
Objective: To assess quality of life of adults with Duchenne muscular dystrophy in the Netherlands a...
Ve své bakalářské práci jsem se zaměřila na kvalitu života u nemocných s myopatií. V teoretické část...
This cost-of-illness analysis based on information from 921 patients in Italy is part of a Europe-wi...
Background: Duchenne Muscular Dystrophy (DMD) is a rapidly progressive, lethal neuromuscular disorde...
Abstract Background Duchenne Muscular Dystrophy (DMD) is a rapidly progressive, lethal neuromuscular...
The purpose of this study was to evaluate the quality of life (QoL) of patients with Duchenne muscul...