Osteogenesis imperfecta type IV (disorder)

Known as: OI, TYPE IV, Osteogenesis imperfecta, type 4, Osteogenesis imperfecta with normal sclerae 
A type of osteogenesis imperfecta that is characterized by fractures and hearing loss. It is more severe than type I and less severe than types II… (More)
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
BACKGROUND Children with osteogenesis imperfecta are often treated with intravenous bisphosphonates. We aimed to assess the… (More)
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Highly Cited
2009
Highly Cited
2009
Mesenchymal stem cells (MSCs) are defined by their ability to self-renew and differentiate into the cells that form mesodermal… (More)
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Highly Cited
2008
Highly Cited
2008
Osteogenesis imperfecta is an inherited disorder characterized by increased bone fragility, fractures, and osteoporosis, and most… (More)
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2007
2007
Cyclical intravenous treatment with pamidronate is of clinical benefit in children with moderate to severe osteogenesis… (More)
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Highly Cited
2002
Highly Cited
2002
Osteogenesis imperfecta (OI) is a heritable disease of bone in which the hallmark is bone fragility. Usually, the disorder is… (More)
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Highly Cited
2002
Highly Cited
2002
Osteogenesis imperfecta (OI) is a heritable disease of bone with low bone mass and bone fragility. The disease is generally… (More)
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Highly Cited
1999
Highly Cited
1999
In principle, transplantation of mesenchymal progenitor cells would attenuate or possibly correct genetic disorders of bone… (More)
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Highly Cited
1999
Highly Cited
1999
BACKGROUND Calcification of the media of peripheral arteries is referred to as Mönckeberg's sclerosis (MS) and occurs commonly in… (More)
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1999
1999
OBJECTIVES To describe the clinical and neuroradiological features of basilar impression in patients with osteogenesis imperfecta… (More)
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1988
1988
To resolve uncertainty concerning the inheritance of the perinatal lethal form of osteogenesis imperfecta (OI type II), we… (More)
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