TY  - JOUR
AU  - Blom, Dirk J
AU  - O'Dea, Louis
AU  - Digenio, Andres
AU  - Alexander, Veronica J
AU  - Karwatowska-Prokopczuk, Ewa
AU  - Williams, Karren R
AU  - Hemphill, Linda
AU  - Muñiz-Grijalvo, Ovidio
AU  - Santos, Raul D
AU  - Baum, Seth
AU  - Witztum, Joseph L
PY  - 2018
DO  - 10.1016/j.jacl.2018.05.013
SN  - 1933-2874
UR  - http://hdl.handle.net/10668/13078
T2  - Journal of clinical lipidology
AB  - Familial chylomicronemia syndrome (FCS) is a rare metabolic disorder caused by mutations in lipoprotein lipase (LPL) or genes required for LPL functionality and is characterized by hyperchylomicronemia that results in recurrent episodes of acute...
LA  - en
KW  - Acute pancreatitis
KW  - Chylomicronemia
KW  - Extremely restrictive low-fat diet
KW  - Familial Chylomicronemia Syndrome
KW  - Hyperlipoproteinemia
KW  - Hypertriglyceridemia
KW  - Lipoprotein lipase deficiency
KW  - Natural history
KW  - Adult
KW  - Cohort Studies
KW  - Female
KW  - Humans
KW  - Hyperlipoproteinemia Type I
KW  - Male
KW  - Middle Aged
KW  - Oligonucleotides
KW  - Treatment Outcome
KW  - Young Adult
TI  - Characterizing familial chylomicronemia syndrome: Baseline data of the APPROACH study.
TY  - research article
VL  - 12
ER  -