Why are behaviors of children suffering from various neuronopathic types of mucopolysaccharidoses different?
- 21 August 2010
- journal article
- research article
- Published by Elsevier BV in Medical Hypotheses
- Vol. 75 (6), 605-609
- https://doi.org/10.1016/j.mehy.2010.07.044
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Pathophysiology of neuropathic lysosomal storage disordersJournal of Inherited Metabolic Disease, 2010
- Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutationMolecular Genetics and Metabolism, 2009
- Correlation between severity of mucopolysaccharidoses and combination of the residual enzyme activity and efficiency of glycosaminoglycan synthesisActa Paediatrica, 2009
- Genistein-mediated inhibition of glycosaminoglycan synthesis, which corrects storage in cells of patients suffering from mucopolysaccharidoses, acts by influencing an epidermal growth factor-dependent pathwayJournal of Biomedical Science, 2009
- Secondary lipid accumulation in lysosomal diseaseBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 2008
- Animal models for mucopolysaccharidosis disorders and their clinical relevanceActa Paediatrica, 2007
- Secondary accumulation of gangliosides in lysosomal storage disordersSeminars in Cell & Developmental Biology, 2004
- A general model for genetic regulation of turnover of glycosaminoglycans suggests a possible procedure for prediction of severity and clinical progress of mucopolysaccharidosesMedical Hypotheses, 2004
- Neurochemical Characterization of Canine α‐L‐Iduronidase Deficiency Disease (Model of Human Mucopolysaccharidosis I)Journal of Neurochemistry, 1985
- Decreased ganglioside neuraminidase activity in fibroblasts from mucopolysaccharidosis patients Inhibition of the activity in vitro by sulfated glycosaminoglycans and other compoundsBiochimica et Biophysica Acta (BBA) - General Subjects, 1983