Romano-Ward Syndrome

Known as: Long QT Syndrome Type 1, LQT1, Romano Ward Syndrome 
A form of long QT syndrome that is without congenital deafness. It is caused by mutation of the KCNQ1 gene which encodes a protein in the VOLTAGE… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1976-2018
010203019762018

Papers overview

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2009
2009
BACKGROUND Body sway increases with age. The purpose of this study was to obtain baseline data and the characteristics of balance… (More)
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2008
2008
Selection operator is one of the important aspects in the GA process. There are several ways for selection. Some of them are… (More)
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2004
2004
Inherited long QT syndrome is most frequently associated with mutations in KCNQ1, which encodes the primary subunit of a… (More)
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Highly Cited
2004
Highly Cited
2004
Ghrelin, identified in the gastric mucosa has been involved in control of food intake and growth hormone (GH) release but little… (More)
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2004
2004
Romano-Ward syndrome (RWS), the autosomal dominant form of the congenital long QT syndrome, is characterised by prolongation of… (More)
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Highly Cited
2004
Highly Cited
2004
Wolcott-Rallison syndrome (WRS) is a rare autosomal-recessive disorder characterized by the association of permanent neonatal or… (More)
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Highly Cited
2003
Highly Cited
2003
AbstractHutchinson-Gilford progeria syndrome (HGPS; MIM 176670) is an extremely rare disease that is characterized by accelerated… (More)
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Highly Cited
2000
Highly Cited
2000
OBJECTIVES To define the cellular mechanisms responsible for the development of life-threatening arrhythmias in response to… (More)
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Highly Cited
1997
Highly Cited
1997
BACKGROUND KVLQT1, the gene encoding the alpha-subunit of a cardiac potassium channel, is the most common cause of the dominant… (More)
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1980
1980
About syncopal attacks caused by cardial arrhythmias had been frequently reported. In one family we found female members of three… (More)
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