Enzyme replacement therapy (ERT) is the worldwide standard of care for a number of mucopolysaccharidosis (MPS) diseases. We report a kinetic study of plasmatic dermatan sulfate (DS) in a 3-year-old subject affected by a severe form of MPS II during the first 10 months of ERT with Idursulfase. A strong increase in the DS plasmatic concentration was measured immediately after the first enzyme infusion, with a maximum after 3 h, followed by a continuous decrease in the 8-15 days following the beginning of treatment. After this, a constant plasmatic content of DS concentration was observed. Overall, during the 10-month treatment period, ERT reduced the plasmatic concentration of DS up to ~80-85 %, but it was unable to totally remove it from the...
Copyright © 2006 American Association for Clinical Chemistry, Inc.BackgroundMucopolysaccharidosis ty...
Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive disorder caused by a deficiency of N-a...
Background:Mucopolysaccharidosis type II (MPS II) is a lysosomal storage disorder related to a defic...
Enzyme replacement therapy (ERT) is the worldwide standard of care for a number of mucopolysaccharid...
We report the structural characterization of plasmatic and urinary GAGs in a patientaffected by MPS ...
We report the structural characterization of plasmatic and urinary GAGs in a Patient affected by MPS...
Enzyme-replacement therapy (ERT) is a new option for the clinical management of MPS I, However, no d...
Enzyme-replacement therapy (ERT) is a new option for the clinical management of MPS I. However, no d...
Backgroung To date, only few data are available on the capacity of ERT at standard doses to defini...
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease caused by deficiency of -L-iduro...
The evaluation of plasmatic galactosaminoglycans, dermatan sulfate (DS) and chondroitin sulfate (CS)...
Mucopolysaccharidosis type II (MPS II) is a multisystemic lysosomal storage disorder caused by defic...
The evaluation of plasmatic galactosaminoglycans, dermatan sulfate (DS) and chondroitin sulfate (CS)...
Plasmatic and urinary glycosaminoglycans characterization in mucopolysaccharidosis II patient treate...
Objective To assess the relationship between anti-Iduronate 2-sulfatase (IDS) antibodies, IDS genoty...
Copyright © 2006 American Association for Clinical Chemistry, Inc.BackgroundMucopolysaccharidosis ty...
Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive disorder caused by a deficiency of N-a...
Background:Mucopolysaccharidosis type II (MPS II) is a lysosomal storage disorder related to a defic...
Enzyme replacement therapy (ERT) is the worldwide standard of care for a number of mucopolysaccharid...
We report the structural characterization of plasmatic and urinary GAGs in a patientaffected by MPS ...
We report the structural characterization of plasmatic and urinary GAGs in a Patient affected by MPS...
Enzyme-replacement therapy (ERT) is a new option for the clinical management of MPS I, However, no d...
Enzyme-replacement therapy (ERT) is a new option for the clinical management of MPS I. However, no d...
Backgroung To date, only few data are available on the capacity of ERT at standard doses to defini...
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease caused by deficiency of -L-iduro...
The evaluation of plasmatic galactosaminoglycans, dermatan sulfate (DS) and chondroitin sulfate (CS)...
Mucopolysaccharidosis type II (MPS II) is a multisystemic lysosomal storage disorder caused by defic...
The evaluation of plasmatic galactosaminoglycans, dermatan sulfate (DS) and chondroitin sulfate (CS)...
Plasmatic and urinary glycosaminoglycans characterization in mucopolysaccharidosis II patient treate...
Objective To assess the relationship between anti-Iduronate 2-sulfatase (IDS) antibodies, IDS genoty...
Copyright © 2006 American Association for Clinical Chemistry, Inc.BackgroundMucopolysaccharidosis ty...
Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive disorder caused by a deficiency of N-a...
Background:Mucopolysaccharidosis type II (MPS II) is a lysosomal storage disorder related to a defic...