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Andrea Schenone Selected Research
Andrea Schenone Research Topics
Disease
2
Glycogen Storage Disease Type II (Pompe's Disease)
01/2019 - 01/2018
1
Mucopolysaccharidosis I (Hurler Syndrome)
01/2021
1
Hypersensitivity (Allergy)
01/2021
1
Eye Diseases (Eye Disease)
01/2021
1
Inborn Genetic Diseases (Disease, Hereditary)
01/2019
1
Pain (Aches)
12/2016
1
Fabry Disease (Fabry's Disease)
12/2016
1
Bone Diseases (Bone Disease)
10/2016
1
Lysosomal Storage Diseases (Lysosomal Storage Disease)
06/2014
1
Mucopolysaccharidosis VI (Syndrome, Maroteaux-Lamy)
06/2014
1
Mucolipidoses (Sialidosis)
03/2013
1
Mucopolysaccharidoses
03/2013
1
Mucopolysaccharidosis IV (Morquio Syndrome)
03/2013
1
Multiple Sulfatase Deficiency Disease (Mucosulfatidosis)
03/2013
1
Trifunctional Protein Deficiency With Myopathy And Neuropathy
08/2012
1
Tay-Sachs Disease
05/2012
Drug/Important Bio-Agent (IBA)
3
Enzymes
IBA
01/2018 - 03/2013
2
alpha-Glucosidases (Acid Maltase)
IBA
01/2019 - 01/2018
1
Acids
IBA
01/2018
1
Galactosidases
IBA
12/2016
1
N-Acetylgalactosamine-4-Sulfatase (Arylsulfatase B)
IBA
06/2014
1
Dermatan Sulfate
IBA
06/2014
1
Glycosaminoglycans
IBA
03/2013
1
Sulfatases
IBA
03/2013
1
Fatty Acids (Saturated Fatty Acids)
IBA
08/2012
1
Hexosaminidase A (Hex A)
IBA
05/2012
Therapy/Procedure
2
Enzyme Replacement Therapy
01/2021 - 06/2014
2
Therapeutics
12/2016 - 10/2016
1
Splenectomy
10/2016