نتایج جستجو برای: becker muscular dystrophy

تعداد نتایج: 55949  

Journal: :Neuromuscular disorders : NMD 2005
Francesco Muntoni Kate Bushby Gertjan van Ommen

Twenty-six participants including parents, scientists, industry representatives and clinicians from Australia, Belgium, England, France, The Netherlands, and USA attended the 128th ENMC workshop on the topic of ‘Preclinical optimization and Phase I/II Clinical Trials Using Antisense Oligonucleotides in Duchenne Muscular Dystrophy’. The meeting was held in Naarden, The Netherlands, during the we...

Journal: :Journal of Methods and Measurement in the Social Sciences 2011

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2016
Jean K Mah Lawrence Korngut Kirsten M Fiest Jonathan Dykeman Lundy J Day Tamara Pringsheim Nathalie Jette

BACKGROUND The muscular dystrophies are a heterogeneous group of genetic muscle diseases with variable distribution of weakness and mode of inheritance. METHODS We previously performed a systematic review of worldwide population-based studies on Duchenne and Becker muscular dystrophies; the current study focused on the epidemiology of other muscular dystrophies using Medline and EMBASE databa...

2014
LORENZA MAGLIANO MARIA GRAZIA D'ANGELO GIUSEPPE VITA MARIKA PANE ADELE D'AMICO UMBERTO BALOTTIN CORRADO ANGELINI ROBERTA BATTINI LUISA POLITANO MELANIA PATALANO ALESSANDRA SAGLIOCCHI FEDERICA CIVATI ERIKA BRIGHINA GIAN LUCA VITA SONIA MESSINA MARIA SFRAMELI MARIA ELENA LOMBARDO ROBERTA SCALISE GIULIA COLIA MARIA CATTERUCCIA ANGELA BERARDINELLI MARIA CHIARA MOTTA ALESSANDRA GAIANI CLAUDIO SEMPLICINI LUCA BELLO GUJA ASTREA ANTONELLA ZACCARO MARIANNA SCUTIFERO

This study explored the burden in parents and healthy siblings of 4-17 year-old patients with Duchenne (DMD) and Becker (BMD) muscular dystrophies, and whether the burden varied according to clinical aspects and social resources. Data on socio-demographic characteristics, patient's clinical history, parent and healthy children burden, and on parent's social resources were collected using self-r...

2007
Robert Jones

There have been few publications relating to limb girdle muscular dystrophy (LGMD) in India. In this issue Meena et al describe clinical and pathological features of 26 LGMD patients from South India. The LGMDs are an expanding group of diverse conditions, the term LGMD was first introduced in 1954 by Natrass and Walton to and there is reduced calpain on Western Blot analysis. LGMD2B is caused ...

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