Ladislav Kuchar Selected Research

Sphingolipid Activator Proteins

2/2009

Prosaposin 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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Ladislav Kuchar Research Topics

Disease

2	Fabry Disease (Fabry's Disease) 01/2018 - 03/2015
1	Asthma (Bronchial Asthma) 01/2021
1	Niemann-Pick Diseases (Niemann Pick Disease) 01/2019
1	Hypoxia (Hypoxemia) 01/2018
1	Disease Progression 09/2017
1	Mucolipidoses (Sialidosis) 09/2017
1	Lysosomal Storage Diseases (Lysosomal Storage Disease) 03/2015
1	Combined Saposin Deficiency 02/2009
1	Metachromatic Leukodystrophy (Sulfatide Lipidosis) 02/2009
1	Metachromatic Leukodystrophy due to Saposin B Deficiency 02/2009

Drug/Important Bio-Agent (IBA)

3	LipidsIBA 01/2021 - 02/2009
3	SphingolipidsIBA 01/2021 - 02/2009
2	globotriaosylceramide (globotriosylceramide)IBA 01/2018 - 03/2015
1	LeukotrienesIBA 01/2021
1	Sphingomyelin Phosphodiesterase (Sphingomyelinase)IBA 01/2019
1	GlycoconjugatesIBA 01/2018
1	Sulfoglycosphingolipids (Sulfatides)IBA 01/2018
1	Blood Group Antigens (Blood Groups)IBA 01/2018
1	miglustat (Zavesca)FDA Link 09/2017
1	GalactosidasesIBA 03/2015
1	ArylsulfatasesIBA 02/2009
1	Proteins (Proteins, Gene)FDA Link 02/2009
1	Sphingolipid Activator ProteinsIBA 02/2009
1	SaposinsIBA 02/2009