Andrea Schenone Selected Research

Dermatan Sulfate

6/2014

[Mucopolysaccharidosis type VI: clinical aspects, diagnosis and treatment with enzyme replacement therapy].

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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	EnzymesIBA 01/2018 - 03/2013
2	alpha-Glucosidases (Acid Maltase)IBA 01/2019 - 01/2018
1	AcidsIBA 01/2018
1	GalactosidasesIBA 12/2016
1	N-Acetylgalactosamine-4-Sulfatase (Arylsulfatase B)IBA 06/2014
1	Dermatan SulfateIBA 06/2014
1	GlycosaminoglycansIBA 03/2013
1	SulfatasesIBA 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