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L P Aggerbeck Selected Research

Malabsorption Syndromes (Malabsorption Syndrome)

12/2008Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities.
8/2007Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes.
11/2001Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's disease.
5/2000[Microsomal triglyceride transfer protein and abetalipoproteinemia].

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L P Aggerbeck Research Topics

Disease

4Malabsorption Syndromes (Malabsorption Syndrome)
12/2008 - 05/2000
4Abetalipoproteinemia (Bassen Kornzweig Syndrome)
08/2007 - 01/2000
2Avitaminosis (Vitamin Deficiency)
05/2000 - 01/2000
1Chylomicron retention disease
12/2008
1Liver Diseases (Liver Disease)
12/2008
1Muscle Weakness
05/2000
1Diarrhea
05/2000
1Malnutrition (Nutritional Deficiencies)
01/2000
1Inborn Genetic Diseases (Disease, Hereditary)
01/2000

Drug/Important Bio-Agent (IBA)

5LipidsIBA
12/2008 - 01/2000
3ChylomicronsIBA
08/2007 - 01/2000
3microsomal triglyceride transfer proteinIBA
11/2001 - 01/2000
2Lipoproteins (Lipoprotein)IBA
11/2001 - 01/2000
2Proteins (Proteins, Gene)FDA Link
11/2001 - 01/2000
2VLDL LipoproteinsIBA
05/2000 - 01/2000
2CholesterolIBA
05/2000 - 01/2000
2Triglycerides (Triacylglycerol)IBA
05/2000 - 01/2000
1Transaminases (Aminotransferases)IBA
12/2008
1Creatine Kinase (Creatine Phosphokinase)IBA
12/2008
1Glycoside Hydrolases (Endoglycosidases)IBA
11/2001
1OligosaccharidesIBA
11/2001
1Apolipoprotein B-48IBA
11/2001
1Brefeldin AIBA
11/2001
1VitaminsIBA
05/2000
1ApolipoproteinsIBA
05/2000

Therapy/Procedure

1Therapeutics
05/2000
1Fat-Restricted Diet (Diet, Fat Restricted)
05/2000