A new familial, autosomal dominant, myopathy and variant of hereditary inclusion body myopathy (HIBM) is described in 19 members of a large Swedish family followed in the Departments of Pediatrics, Genetics, and Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
Hereditary inclusion bodymyopathy (HIBM) is an adult onset, slowly progressive distal and proximal m...
International audienceIntroduction: Hereditary inclusion body myopathy (hIBM) refers to a group of c...
Contains fulltext : 69402.pdf (publisher's version ) (Closed access)Hereditary inc...
The term hereditary inclusion-body myopathies (HIBMs) defines a group of rare muscle disorders with ...
Hereditary inclusion body myopathy (HIBM) is a unique disorder of unknown etiology that typically oc...
AbstractThe term hereditary inclusion-body myopathies (HIBMs) defines a group of rare muscle disorde...
Hereditary inclusion body myopathy (HIBM; OMIM 600737) is a unique group of neuromuscular disorders ...
Item does not contain fulltextWe present a comprehensive report of two siblings with hereditary incl...
Hereditary inclusion-body myopathy (h-IBM), or distal myopathy with rimmed vacuoles (DMRV), is an au...
The hereditary inclusion-body myopathies encompass several syndromes with autosomal recessive or dom...
AbstractHereditary Inclusion Body Myopathy (HIBM) is an autosomal recessive, quadriceps sparing type...
Hereditary Inclusion Body Myopathy (HIBM) is a rare autosomal dominant or recessive adult onset musc...
Sporadic inclusion-body myositis (sIBM) is the most common acquired muscle disease in Caucasians ove...
Hereditary Inclusion Body Myopathy (HIBM) is a rare autosomal dominant or recessive adult onset musc...
Autosomal dominant myopathy, Paget disease of bone, and dementia constitute a unique disorder (MIM 6...
Hereditary inclusion bodymyopathy (HIBM) is an adult onset, slowly progressive distal and proximal m...
International audienceIntroduction: Hereditary inclusion body myopathy (hIBM) refers to a group of c...
Contains fulltext : 69402.pdf (publisher's version ) (Closed access)Hereditary inc...
The term hereditary inclusion-body myopathies (HIBMs) defines a group of rare muscle disorders with ...
Hereditary inclusion body myopathy (HIBM) is a unique disorder of unknown etiology that typically oc...
AbstractThe term hereditary inclusion-body myopathies (HIBMs) defines a group of rare muscle disorde...
Hereditary inclusion body myopathy (HIBM; OMIM 600737) is a unique group of neuromuscular disorders ...
Item does not contain fulltextWe present a comprehensive report of two siblings with hereditary incl...
Hereditary inclusion-body myopathy (h-IBM), or distal myopathy with rimmed vacuoles (DMRV), is an au...
The hereditary inclusion-body myopathies encompass several syndromes with autosomal recessive or dom...
AbstractHereditary Inclusion Body Myopathy (HIBM) is an autosomal recessive, quadriceps sparing type...
Hereditary Inclusion Body Myopathy (HIBM) is a rare autosomal dominant or recessive adult onset musc...
Sporadic inclusion-body myositis (sIBM) is the most common acquired muscle disease in Caucasians ove...
Hereditary Inclusion Body Myopathy (HIBM) is a rare autosomal dominant or recessive adult onset musc...
Autosomal dominant myopathy, Paget disease of bone, and dementia constitute a unique disorder (MIM 6...
Hereditary inclusion bodymyopathy (HIBM) is an adult onset, slowly progressive distal and proximal m...
International audienceIntroduction: Hereditary inclusion body myopathy (hIBM) refers to a group of c...
Contains fulltext : 69402.pdf (publisher's version ) (Closed access)Hereditary inc...
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