International audienceMonoclonal gammopathy of unknow significance (MGUS) has recently been described as a possible cause of sporadic late onset nemaline myopathy (SLONM), which can lead to severe muscle impairment and respiratory insufficiency. We report the case of a man presenting a MGUS related SLONM, whose singularity was a severe heart involvement..
Nemaline myopathy, which is characterized by the accumulation of "rod" bodies in muscle fibers is a ...
BackgroundNemaline myopathies are congenital or acquired muscle disorders that typically present in ...
International audienceObjective: Monoclonal gammopathy have been related with numerous neurological ...
International audienceMonoclonal gammopathy of unknow significance (MGUS) has recently been describe...
Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline...
Sporadic late onset nemaline myopathy (SLONM) is a rare acquired form of myopathy. The disease progr...
Sporadic late-onset nemaline myopathy (SLONM) is a rare acquired myopathy characterized by rapid-ons...
Abstract Monoclonal gammopathy of undetermined significance (MGUS) may be associated with pathologie...
OBJECTIVE: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset myopathy that progres...
Item does not contain fulltextOBJECTIVE: Sporadic late-onset nemaline myopathy (SLONM) is a rare, la...
Objective: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset myopathy that progres...
BackgroundSporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, chara...
BACKGROUND: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, cha...
Background: Nemaline myopathy is a rare, non progressive congenital skeletal muscle disorder defined...
Background: Neuromuscular pathologies must be considered when caring for patients with persistent or...
Nemaline myopathy, which is characterized by the accumulation of "rod" bodies in muscle fibers is a ...
BackgroundNemaline myopathies are congenital or acquired muscle disorders that typically present in ...
International audienceObjective: Monoclonal gammopathy have been related with numerous neurological ...
International audienceMonoclonal gammopathy of unknow significance (MGUS) has recently been describe...
Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline...
Sporadic late onset nemaline myopathy (SLONM) is a rare acquired form of myopathy. The disease progr...
Sporadic late-onset nemaline myopathy (SLONM) is a rare acquired myopathy characterized by rapid-ons...
Abstract Monoclonal gammopathy of undetermined significance (MGUS) may be associated with pathologie...
OBJECTIVE: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset myopathy that progres...
Item does not contain fulltextOBJECTIVE: Sporadic late-onset nemaline myopathy (SLONM) is a rare, la...
Objective: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset myopathy that progres...
BackgroundSporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, chara...
BACKGROUND: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, cha...
Background: Nemaline myopathy is a rare, non progressive congenital skeletal muscle disorder defined...
Background: Neuromuscular pathologies must be considered when caring for patients with persistent or...
Nemaline myopathy, which is characterized by the accumulation of "rod" bodies in muscle fibers is a ...
BackgroundNemaline myopathies are congenital or acquired muscle disorders that typically present in ...
International audienceObjective: Monoclonal gammopathy have been related with numerous neurological ...