Lipoidosis

Known as: Lipoid storage disease NOS, diseases lipid storage, Lipidosis 
Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes… (More)

Topic mentions per year

Topic mentions per year

1944-2017
0204019442016

Papers overview

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Highly Cited
2011
Highly Cited
2011
Peroxisome proliferator-activated receptors (PPARs) are nuclear hormone receptors that regulate genes involved in energy… (More)
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Highly Cited
2007
Highly Cited
2007
Mammalian and in vitro studies have raised concerns about the toxicity of titanium dioxide nanoparticles (TiO2 NPs), but there… (More)
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Highly Cited
2007
Highly Cited
2007
Neutral lipid storage disease comprises a heterogeneous group of autosomal recessive disorders characterized by systemic… (More)
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Highly Cited
2007
Highly Cited
2007
Dairy cows are highly susceptible after parturition to developing liver lipidosis and ketosis, which are costly diseases to… (More)
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Highly Cited
2007
Highly Cited
2007
Mammalian studies have raised concerns about the toxicity of carbon nanotubes (CNTs), but there is very limited data on… (More)
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Highly Cited
2002
Highly Cited
2002
We recently showed that human skin fibroblasts internalize fluorescent analogues of the glycosphingolipids lactosylceramide and… (More)
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Highly Cited
2001
Highly Cited
2001
Niemann-Pick type C (NPC) disease is a cholesterol lipidosis caused by mutations in NPC1 and NPC2 gene loci. Most human cases are… (More)
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Highly Cited
1999
Highly Cited
1999
We have calculated the relative frequency and the birth prevalence of lysosomal storage diseases (LSDs) in The Netherlands based… (More)
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Highly Cited
1998
Highly Cited
1998
Acetaminophen (APAP) hepatotoxicity is due to its biotransformation to a reactive metabolite, N-acetyl-p-benzoquinone imine… (More)
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Highly Cited
1974
Highly Cited
1974
Although the usual diet may contain 150-250 mg of plant sterols, chiefly beta-sitosterol, only trace amounts of these sterols… (More)
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