Osteogenesis Imperfecta, Type V

Known as: OI, TYPE V, OI5 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1966-2017
02419662017

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2017
2017
was verv profuse, but chiefly venous, and was readily controlled by pressure^ and the wound was afterwards lightly dressed… (More)
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2017
2017
INTRODUCTION Following the 2005-6 chikungunya outbreak, a project to strengthen regional Public Health preparedness in the Indian… (More)
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Review
2015
Review
2015
BACKGROUND A better understanding of the natural history of osteogenesis imperfecta (OI) in adulthood should improve health care… (More)
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2012
2012
Osteogenesis imperfecta (OI), also known as ‘‘brittle bone disease’’, is a rare genetic disorder of collagen tissues… (More)
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2011
2011
Key theories of autism implicate orbitofrontal cortex (OFC) compromise, while olfactory identification (OI) deficits are… (More)
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2011
2011
We report a large consanguineous Turkish family in which multiple individuals are affected with autosomal recessive lethal or… (More)
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2006
2006
OBJECTIVE To determine whether first- and second-trimester Down syndrome screening markers and screen-positive rates are altered… (More)
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1999
1999
We utilized the Cre/lox recombination system to develop the first knock-in murine model for osteogenesis imperfecta (OI). The… (More)
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1980
1980
The prostanoid 3-oxa-4,5,6-trinor-3,7-inter-m-phenylene PGE1 (OI-PGE1) has been shown to be a more potent inhibitor of ADP… (More)
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1968
1968
A series of IOO lead workers from different industries, 9I at work and nine admitted to hospital with lead poisoning, was studied… (More)
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