Neuromuscular diorders can be divided into 1) myopathies, primary disease of themuscle fiber, 2) myasthenias, diseases caused by defects of the neuromuscular junction and 3)neurogenic muscular atrophies, caused by the defects of the motor nerve. Musculardystrophies are a heterogeneous group of myopathies. They are genetic disorders caused bymuscle fiber degeneration often causing progressive weakness and wasting and they can befurther divided into the followingMyotonic dystrophies – DM1 andDM2Dystrophinopathies - DMD, BMDFacioscapulohumeral - FSHDLimb-girdle – LGMD subtypesDistal muscular dystrophiesCongenital dystrophies - CMDOculofaryngeal - OPM, OPDMEmery-Dreifuss - X-EMD, AD-EMDOther and unclassified muscular dystrophie
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Objective: To apply next-generation sequencing (NGS) for the investigation of the genetic basis of u...
Neuromuscular diorders can be divided into 1) myopathies, primary disease of themuscle fiber, 2) mya...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
AbstractMyotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autoso...
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal domi...
Myotonic dystrophies (DM) are the most common muscular dystrophies in adults, which can affect other...
AbstractMyotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autoso...
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal domi...
Myotonic dystrophy type 1 (DM1 or Steinert's disease) and type 2 (DM2) are multisystem disorders of ...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Objective: To apply next-generation sequencing (NGS) for the investigation of the genetic basis of u...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Objective: To apply next-generation sequencing (NGS) for the investigation of the genetic basis of u...
Neuromuscular diorders can be divided into 1) myopathies, primary disease of themuscle fiber, 2) mya...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
AbstractMyotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autoso...
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal domi...
Myotonic dystrophies (DM) are the most common muscular dystrophies in adults, which can affect other...
AbstractMyotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autoso...
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal domi...
Myotonic dystrophy type 1 (DM1 or Steinert's disease) and type 2 (DM2) are multisystem disorders of ...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Objective: To apply next-generation sequencing (NGS) for the investigation of the genetic basis of u...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Objective: To apply next-generation sequencing (NGS) for the investigation of the genetic basis of u...