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Wolfram Syndrome

Known as: DIDMOAD, WFS, Syndrome, Wolfram 
A hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This… Expand
National Institutes of Health

Papers overview

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Review
2017
Review
2017
The endoplasmic reticulum (ER) is the organelle where secretory and membrane proteins are synthesized and folded. Unfolded… Expand
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Highly Cited
2010
Highly Cited
2010
Wolfram syndrome is an autosomal-recessive disorder characterized by insulin-dependent diabetes mellitus, caused by nonautoimmune… Expand
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Review
2009
Review
2009
Hearing impairment is the most common sensory disorder, present in 1 of every 500 newborns. With 46 genes implicated in… Expand
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Highly Cited
2003
Highly Cited
2003
Who knows what I want to do? Who knows what anyone wants to do? How can you be sure about something like that? Isn’t it all a… Expand
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Highly Cited
2003
Highly Cited
2003
Mutations of the WFS1 gene are responsible for Wolfram syndrome, a rare, recessive disorder characterized by early-onset, non… Expand
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Highly Cited
2002
Highly Cited
2002
In June 2000, after two years of fairly smooth operation, California's deregulated wholesale electricity market began producing… Expand
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Highly Cited
2001
Highly Cited
2001
Wolfram (DIDMOAD) syndrome is an autosomal recessive neurodegenerative disorder accompanied by insulin-dependent diabetes… Expand
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Highly Cited
1998
Highly Cited
1998
Wolfram syndrome (WFS; OMIM 222300) is an autosomal recessive neurodegenerative disorder defined by young-onset non-immune… Expand
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Review
1997
Review
1997
Wolfram syndrome (MIM 222300) is the association of juvenile onset diabetes mellitus and optic atrophy, also known as DIDMOAD… Expand
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Highly Cited
1995
Highly Cited
1995
Wolfram syndrome is the association of diabetes mellitus and optic atrophy, and is sometimes called DIDMOAD (diabetes insipidus… Expand
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