The heart and lung are in continuous reciprocal interaction that creates a functional and anatomical reserve referred to as cardiopulmonary coupling (CPC). Disruption of CPC can occur due to various cardiac or pulmonary pathologies but also can occur in patients with myopathies. Nemaline myopathy (NM) is a skeletal muscle heterogeneous disorder due to contractile proteins' gene mutations that impact lung and cardiac mechanics and thus is expected to adversely affect CPC in a complex manner. We present a case of NM and we review the literature on cardiac and pulmonary effects of myopathy-related disruption of CPC.</p
ABSTRACT: Congenital myopathies are a group of primary hereditary, clinically and genetically hetero...
Background Bethlem myopathy is considered a relatively mild neuromuscular disorder without signific...
Nemaline myopathy (NM) is a congenital neuromuscular disorder with heterogeneous clinical signs such...
The heart and lung are in continuous reciprocal interaction that creates a functional and anatomical...
The heart and lung are in continuous reciprocal interaction that creates a functional and anatomical...
Background: Nemaline myopathy is a rare, non progressive congenital skeletal muscle disorder defined...
Mutations have been identified in alpha-tropomyosin (Tm), a key regulatory protein in striated muscl...
Nemaline myopathy is a rare congenital disease that generally occurs in childhood. We report a case...
The congenital myopathies are a group of early-onset, non-dystrophic neuromuscular conditions with c...
Nemaline myopathy, which is characterized by the accumulation of "rod" bodies in muscle fibers is a ...
Nemaline myopathies are a heterogenous group of congenital myopathies caused by de novo, dominantly ...
Nemaline myopathy (NM) is among the most common non-dystrophic congenital myopathies (incidence 1:50...
Mutations have been identified in α-tropomyosin (Tm), a key regulatory protein in striated muscle ce...
International audienceMonoclonal gammopathy of unknow significance (MGUS) has recently been describe...
Nemaline myopathy is a rare congenital myopathy that generally presents in childhood. We report a ca...
ABSTRACT: Congenital myopathies are a group of primary hereditary, clinically and genetically hetero...
Background Bethlem myopathy is considered a relatively mild neuromuscular disorder without signific...
Nemaline myopathy (NM) is a congenital neuromuscular disorder with heterogeneous clinical signs such...
The heart and lung are in continuous reciprocal interaction that creates a functional and anatomical...
The heart and lung are in continuous reciprocal interaction that creates a functional and anatomical...
Background: Nemaline myopathy is a rare, non progressive congenital skeletal muscle disorder defined...
Mutations have been identified in alpha-tropomyosin (Tm), a key regulatory protein in striated muscl...
Nemaline myopathy is a rare congenital disease that generally occurs in childhood. We report a case...
The congenital myopathies are a group of early-onset, non-dystrophic neuromuscular conditions with c...
Nemaline myopathy, which is characterized by the accumulation of "rod" bodies in muscle fibers is a ...
Nemaline myopathies are a heterogenous group of congenital myopathies caused by de novo, dominantly ...
Nemaline myopathy (NM) is among the most common non-dystrophic congenital myopathies (incidence 1:50...
Mutations have been identified in α-tropomyosin (Tm), a key regulatory protein in striated muscle ce...
International audienceMonoclonal gammopathy of unknow significance (MGUS) has recently been describe...
Nemaline myopathy is a rare congenital myopathy that generally presents in childhood. We report a ca...
ABSTRACT: Congenital myopathies are a group of primary hereditary, clinically and genetically hetero...
Background Bethlem myopathy is considered a relatively mild neuromuscular disorder without signific...
Nemaline myopathy (NM) is a congenital neuromuscular disorder with heterogeneous clinical signs such...