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Befekadu Asfaw Selected Research

Sphingolipid Activator Proteins

2/2009Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations.

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Befekadu Asfaw Research Topics

Disease

4Fabry Disease (Fabry's Disease)
01/2018 - 07/2002
2Metachromatic Leukodystrophy (Sulfatide Lipidosis)
10/2013 - 02/2009
1Type C Niemann-Pick Disease (Niemann Pick Disease, Type C)
01/2022
1Lysosomal Storage Diseases (Lysosomal Storage Disease)
03/2015
1Sulfatidosis
10/2013
1Metachromatic Leukodystrophy due to Saposin B Deficiency
02/2009
1Combined Saposin Deficiency
02/2009

Drug/Important Bio-Agent (IBA)

2globotriaosylceramide (globotriosylceramide)IBA
01/2018 - 03/2015
2Blood Group Antigens (Blood Groups)IBA
01/2018 - 07/2002
2LipidsIBA
03/2015 - 02/2009
2SphingolipidsIBA
03/2015 - 02/2009
2EnzymesIBA
10/2013 - 06/2008
2alpha-Galactosidase (Beano)IBA
06/2008 - 07/2002
1CholesterolIBA
01/2022
1Dextrans (Dextran)FDA Link
01/2022
1GlycoconjugatesIBA
01/2018
1GalactosidasesIBA
03/2015
1Sulfoglycosphingolipids (Sulfatides)IBA
10/2013
1ArylsulfatasesIBA
02/2009
1Proteins (Proteins, Gene)FDA Link
02/2009
1Sphingolipid Activator ProteinsIBA
02/2009
1SaposinsIBA
02/2009
1GlycosphingolipidsIBA
07/2002
1alpha-N-Acetylgalactosaminidase (N-Acetyl-alpha-D-Galactosaminidase)IBA
07/2002

Therapy/Procedure

1Therapeutics
06/2008