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References in periodicals archive ?
Mucopolysaccharidosis III (MPS III) (Sanfilippo Syndrome ) - Therapeutics under Development by Companies 11
The report provides comprehensive information on the therapeutics under development for Mucopolysaccharidosis II (MPS II) (Hunter Syndrome ), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type.
Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications.
Dr Saqib Ansari said, The median survival for mucopolysaccharidosis I (MPS I) patients is less than 11.
Dr Saqib Ansari said, "The median survival for mucopolysaccharidosis I (MPS I) patients is less than 11.
Clinical manifestations and treatment of mucopolysaccharidosis type I patients in Latin America as compared with the rest of the world.
Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VI.
She suffers from a debilitating metabolic disorder called mucopolysaccharidosis.
Currently therapies are available for only 6 LSDs - Gaucher, Pompe, Fabry, Mucopolysaccharidosis (MPS) I (Hurler syndrome), MPS II (Hunter Syndrome) and MPS VI (MaroteauxLamy).
This report provides information on the therapeutic development for Mucopolysaccharidosis I (MPS I) (Hurler Syndrome ), complete with latest updates, and special features on late-stage and discontinued projects.
Tandem mass spectrometry for the direct assay of lysosomal enzymes in dried blood spots: application to screening newborns for mucopolysaccharidosis I.
ATHX) said that the FDA has granted orphan drug designation to MultiStem, Athersys' proprietary cell therapy, for the treatment of Hurler's syndrome, also known as mucopolysaccharidosis type I or MPS-I.
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