Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

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… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Maternal undernutrition contributes to 800,000 neonatal deaths annually through small for gestational age births; stunting… Expand
  • figure 1
  • table 1
  • table 2
  • table 3
  • table 4
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… Expand
  • figure 1
  • figure 2
  • table 1
  • figure 3
Review
2002
Review
2002
Superoxide dismutases are an ubiquitous family of enzymes that function to efficiently catalyze the dismutation of superoxide… Expand
Review
2000
Review
2000
OBJECTIVE The authors conducted a meta-analysis of relevant data from primary studies of the genetic epidemiology of major… Expand
  • table 1
  • table 2
  • figure 1
  • table 3
Review
2000
Review
2000
There is mounting evidence that inflammation plays a role in the development of coronary heart disease (CHD). Observations have… Expand
Highly Cited
2000
Highly Cited
2000
Amyloid plaques are a neuropathological hallmark of Alzheimer's disease (AD), but their relationship to neurodegeneration and… Expand
  • figure 1
  • figure 2
  • figure 4
  • figure 3
  • figure 5
Review
1998
Review
1998
The prevalence of obesity among children is high and is increasing. We know that obesity runs in families, with children of obese… Expand
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… Expand
Highly Cited
1993
Highly Cited
1993
Apolipoprotein E, type ϵ4 allele (APOE ϵ4), is associated with late-onset familial Alzheimer's disease (AD). There is high… Expand
Highly Cited
1993
Highly Cited
1993
Although patients with thromboembolic disease frequently have family histories of thrombosis, well-defined defects such as… Expand