Oculopharyngodistal Myopathy

Known as: FACIOOCULOLARYNGOPHARYNGEAL MYOPATHY WITH DISTAL AND RESPIRATORY INVOLVEMENT, FOLP-DR, OPDM 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1977-2017
01219772017

Papers overview

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2015
2015
Oculopharyngodistal myopathy (OPDM) is an extremely rare, adult-onset hereditary muscular disease characterized by progressive… (More)
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2013
2013
Oculopharyngodistal myopathy is an extremely rare disease characterised by slowly progressive blepharoptosis, facial and bulbar… (More)
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2011
2011
BACKGROUND Oculopharyngodistal myopathy (OPDM) has been reported as a rare, adult-onset hereditary muscle disease with putative… (More)
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2008
2008
Oculopharyngodistal myopathy is a rare type of hereditary myopathy characterised pathologically by the changes of muscular… (More)
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2007
2007
BACKGROUND The diabetic intrauterine environment is a known risk factor for the development of diabetes in the offspring… (More)
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2006
2006
The colonization of uropathogenic bacteria on urinary catheters resulting in biofilm formation frequently leads to the infection… (More)
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2004
2004
There has been controversy whether oculopharyngodistal myopathy (OPDM) commonly seen in Japan is a distinct disease entity or a… (More)
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2003
2003
We have shown previously (Rondeau, J.-J., McNicoll, N., Gagnon, J., Bouchard, N., Ong, H., and De Léan, A. (1995) Biochemistry 34… (More)
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1998
1998
We investigated two Japanese siblings presenting with oculopharyngodistal myopathy, whose healthy parents were consanguineous. To… (More)
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1977
1977
Some clinical variants of oculopharyngeal dystrophy are known; a rare form is described in this article: the early-adult form of… (More)
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