Clinical and genetic characteristics, prognostic risk factors, and classification of nemaline myopathy (NM) are examined in a study of 143 cases identified at two centers in Australia and North America and reported from the Neurogenetics Research Unit, University of Sydney, Australia; Children’s Hospital, Boston; and other centers
PURPOSE: Nemaline myopathy (NM) is a clinical heterogeneous congenital myopathy characterized by the...
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy. The traditional appro...
Nemaline myopathy represents a group of clinically and genetically heterogeneous neuromuscular disor...
Nemaline myopathy (NM), a structural congenital myopathy, presents a significant clinical and geneti...
Nemaline myopathies are a heterogenous group of congenital myopathies caused by de novo, dominantly ...
Objective: Nemaline myopathy (NM) is a rare neuromuscular condition with clinical and genetic heter...
Objective: To report pathologic findings in 124 Australian and North American cases of primary nemal...
Nemaline rod myopathy (NM) is a rare form of congenital myopathy characterized by slowly progressive...
Nemaline myopathy (NEM) is one of the most common congenital myopathies. A unique subtype, NEM6, map...
International audienceNemaline myopathy (NM) is a rare congenital myopathy characterised by hypotoni...
Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated ...
Nemaline myopathies are a group of genetically determined (autosomal dominant/recessive) congenital ...
Nemaline Myopathy (NM) is a rare genetic disorder that encompasses a large spectrum of myopathies ch...
The nemaline myopathies constitute a large proportion of the congenital or structural myopathies. Co...
Nemaline Myopathy (NM) is a rare genetic disorder that encompasses a large spectrum of myopathies ch...
PURPOSE: Nemaline myopathy (NM) is a clinical heterogeneous congenital myopathy characterized by the...
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy. The traditional appro...
Nemaline myopathy represents a group of clinically and genetically heterogeneous neuromuscular disor...
Nemaline myopathy (NM), a structural congenital myopathy, presents a significant clinical and geneti...
Nemaline myopathies are a heterogenous group of congenital myopathies caused by de novo, dominantly ...
Objective: Nemaline myopathy (NM) is a rare neuromuscular condition with clinical and genetic heter...
Objective: To report pathologic findings in 124 Australian and North American cases of primary nemal...
Nemaline rod myopathy (NM) is a rare form of congenital myopathy characterized by slowly progressive...
Nemaline myopathy (NEM) is one of the most common congenital myopathies. A unique subtype, NEM6, map...
International audienceNemaline myopathy (NM) is a rare congenital myopathy characterised by hypotoni...
Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated ...
Nemaline myopathies are a group of genetically determined (autosomal dominant/recessive) congenital ...
Nemaline Myopathy (NM) is a rare genetic disorder that encompasses a large spectrum of myopathies ch...
The nemaline myopathies constitute a large proportion of the congenital or structural myopathies. Co...
Nemaline Myopathy (NM) is a rare genetic disorder that encompasses a large spectrum of myopathies ch...
PURPOSE: Nemaline myopathy (NM) is a clinical heterogeneous congenital myopathy characterized by the...
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy. The traditional appro...
Nemaline myopathy represents a group of clinically and genetically heterogeneous neuromuscular disor...
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