|1.||Dube, Syamalima: 1 article (09/2014)|
|2.||Linask, Kersti: 1 article (09/2014)|
|3.||Fan, Yingli: 1 article (09/2014)|
|4.||Sanger, Joseph W: 1 article (09/2014)|
|5.||Wang, Jushuo: 1 article (09/2014)|
|6.||Sanger, Jean M: 1 article (09/2014)|
|7.||Han, Mingda: 1 article (09/2014)|
|8.||Pellenz, Christopher: 1 article (09/2014)|
|9.||Dube, Dipak K: 1 article (09/2014)|
|10.||Hayashi, Yukiko: 1 article (01/2013)|
|1.||Muscular Diseases (Myopathy)
02/15/2009 - "It was first described in two families suffering from limb girdle muscle dystrophy type 1 (LGMD 1A), and later identified in a subset of dominant or sporadic patients suffering from myofibrillar myopathy, as well as in a family with spheroid body myopathy. "
01/01/2001 - "[Cytoplasmic body myopathy (spheroid body myopathy)]."
01/01/1993 - "Several of these diseases, including spheroid body myopathy, granulo-filamentous body myopathy and the dystrophinopathies, are familial. "
01/01/1987 - "(2) Congenital myopathies due to persistent organellar regression: focal loss of cross striation, myopathy with lysis of myofibrils, nemaline body myopathy, zebra body myopathy, spheroid body myopathy, myopathy with tubular aggregates, satellite cell myopathy. "
06/01/2005 - "The muscle biopsy disclosed mixed standard to myopathy, denervation and inclusion bodies that are consistent to spheroid body myopathy. "
|2.||Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
01/01/2007 - "Missense mutations in the myotilin-encoding gene cause dominant limb girdle muscular dystrophy type 1A and spheroid body myopathy and are the molecular defect that can cause myofibrillar myopathy. "
12/27/2005 - "A novel mutation in the TTID gene results in the clinical and pathologic phenotype termed "spheroid body myopathy." Mutations in this gene also cause limb-girdle muscular dystrophy 1A and are associated with myofibrillar myopathy."
08/01/2006 - "Several myotilin point mutations have been described in patients with limb-girdle muscular dystrophy type 1A (LGMD1A), myofibrillar myopathy (MFM), spheroid body myopathy (SBM), three similar adult-onset, progressive and autosomal dominant muscular dystrophies. "
|3.||Distal Myopathies (Distal Muscular Dystrophy)
|5.||Neuromuscular Diseases (Neuromuscular Disease)
|2.||Mutant Proteins (Protein, Mutant)
|3.||desmin storage Myopathy