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Oculopharyngodistal Myopathy

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

Papers overview

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2015
2015
Oculopharyngodistal myopathy (OPDM) is an extremely rare, adult-onset hereditary muscular disease characterized by progressive… Expand
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2014
2014
Egypt is arid country in Africa, but has a large hydro geologic potential with many aquifers widely distributed throughout the… Expand
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2012
2012
The Geostationary Fourier Transform Spectrometer (GeoFTS) is an imaging spectrometer designed for an earth science mission to… Expand
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2011
2011
Background:Oculopharyngodistal myopathy (OPDM) has been reported as a rare, adult-onset hereditary muscle disease with putative… Expand
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2008
2008
Oculopharyngodistal myopathy is a rare type of hereditary myopathy characterised pathologically by the changes of muscular… Expand
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2007
2007
Publisher Summary This chapter discusses the hereditary inclusion body myopathy and other rimmed vacuolar myopathies. Hereditary… Expand
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2007
2007
BACKGROUND The diabetic intrauterine environment is a known risk factor for the development of diabetes in the offspring… Expand
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2006
2006
The colonization of uropathogenic bacteria on urinary catheters resulting in biofilm formation frequently leads to the infection… Expand
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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… Expand
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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… Expand
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