Hyperlipoproteinemia Type I

Known as: Familial Chylomicronemia, Familial LPL Deficiencies, LPL DEFICIENCY 
An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1937-2018
020040060019372017

Papers overview

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Review
2017
Review
2017
Animal models of human diseases that accurately recapitulate clinical pathology are indispensable for understanding molecular… (More)
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Review
2017
Review
2017
Amyloid plaques and neurofibrillary tangles (NFTs) in the brain are the neuropathological hallmarks of Alzheimer's disease (AD… (More)
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Highly Cited
2008
Highly Cited
2008
Prostate cancer is the most common cancer affecting males in developed countries. It shows consistent evidence of familial… (More)
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Highly Cited
2006
Highly Cited
2006
Frontotemporal dementia (FTD) is the second most common cause of dementia in people under the age of 65 years. A large proportion… (More)
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Highly Cited
2004
Highly Cited
2004
Amyloid precursor protein (APP) is endoproteolytically processed by BACE1 and gamma-secretase to release amyloid peptides… (More)
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Highly Cited
2000
Highly Cited
2000
Amyloid plaques are a neuropathological hallmark of Alzheimer's disease (AD), but their relationship to neurodegeneration and… (More)
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Highly Cited
2000
Highly Cited
2000
Primary pulmonary hypertension (PPH), characterized by obstruction of pre-capillary pulmonary arteries, leads to sustained… (More)
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Highly Cited
1997
Highly Cited
1997
Parkinson's disease (PD) is a common neurodegenerative disorder with a lifetime incidence of approximately 2 percent. A pattern… (More)
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Highly Cited
1993
Highly Cited
1993
Apolipoprotein E, type epsilon 4 allele (APOE epsilon 4), is associated with late-onset familial Alzheimer's disease (AD). There… (More)
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Highly Cited
1993
Highly Cited
1993
Although patients with thromboembolic disease frequently have family histories of thrombosis, well-defined defects such as… (More)
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