Add to ORKGDistal myopathies belong to a clinically and pathologi-cally heterogeneous group of genetic disorders, where the distal muscles of the upper or lower limbs are selectively or disproportionately affected.
Laing distal myopathy is an autosomal dominant disease due to mutations in the gene encoding for the...
Myofibrilar myopathy is associated with a wide spectrum of clinical phenotypes, affecting individual...
Background: Laing early onset distal myopathy (MPD1) is an autosomal dominant myopathy caused by mut...
Distal myopathies are a group of heterogeneous disorders classified into one broad category due to t...
Distal myopathies are a clinically and genetically het-erogenous group of disorders in which the dis...
Distal myopathies are genetic primary muscle disorders with a prominent weakness at onset in hands a...
Distal myopathies are a group of muscular disorders described in many countries with different inher...
Mutations in over 20 genes are associated with distal myopathies. Yet, many patients remain unresolv...
Background: Distal myopathy with rimmed vacuoles (DMRV) is an autosomal recessive (AR) myopathy char...
The sporadic distal myopathies are uncommon primary muscle diseases, the pathogenesis of which is st...
Distal myopathies constitute of a very heterogeneous group of muscular disorders. Distal myopathies...
Hereditary inclusion-body myopathy (h-IBM), or distal myopathy with rimmed vacuoles (DMRV), is an au...
Distal myopathy with rimmed vacuoles (DMRV) is an autosomal recessive or sporadic early adult-onset ...
Distal myopathies are a group of clinically and pathologically overlapping muscle diseases that are ...
Distal myopathies are a clinically and genetically heterogenous group of disorders in which the dist...
Laing distal myopathy is an autosomal dominant disease due to mutations in the gene encoding for the...
Myofibrilar myopathy is associated with a wide spectrum of clinical phenotypes, affecting individual...
Background: Laing early onset distal myopathy (MPD1) is an autosomal dominant myopathy caused by mut...
Distal myopathies are a group of heterogeneous disorders classified into one broad category due to t...
Distal myopathies are a clinically and genetically het-erogenous group of disorders in which the dis...
Distal myopathies are genetic primary muscle disorders with a prominent weakness at onset in hands a...
Distal myopathies are a group of muscular disorders described in many countries with different inher...
Mutations in over 20 genes are associated with distal myopathies. Yet, many patients remain unresolv...
Background: Distal myopathy with rimmed vacuoles (DMRV) is an autosomal recessive (AR) myopathy char...
The sporadic distal myopathies are uncommon primary muscle diseases, the pathogenesis of which is st...
Distal myopathies constitute of a very heterogeneous group of muscular disorders. Distal myopathies...
Hereditary inclusion-body myopathy (h-IBM), or distal myopathy with rimmed vacuoles (DMRV), is an au...
Distal myopathy with rimmed vacuoles (DMRV) is an autosomal recessive or sporadic early adult-onset ...
Distal myopathies are a group of clinically and pathologically overlapping muscle diseases that are ...
Distal myopathies are a clinically and genetically heterogenous group of disorders in which the dist...
Laing distal myopathy is an autosomal dominant disease due to mutations in the gene encoding for the...
Myofibrilar myopathy is associated with a wide spectrum of clinical phenotypes, affecting individual...
Background: Laing early onset distal myopathy (MPD1) is an autosomal dominant myopathy caused by mut...