Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and S

Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and S

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http://www.wikidata.org/entity/Q33607275

Q33607275

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Developing therapeutic approaches for metachromatic leukodystrophy Bone marrow transplantation improves autoinflammation and inflammatory bone loss in SH3BP2 knock-in cherubism mice Gene therapy for metachromatic leukodystrophy.Microglia as a critical player in both developmental and late-life CNS pathologies.Progression of multiple behavioral deficits with various ages of onset in a murine model of Hurler syndrome.Whole body correction of mucopolysaccharidosis IIIA by intracerebrospinal fluid gene therapy Cell- and gene-based therapeutic approaches for neurological deficits in mucopolysaccharidoses Mucopolysaccharidosis VI.Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone.Systematic approach to the diagnosis of lysosomal storage disorders.Gaucher disease: pathological mechanisms and modern management.Angiokeratoma corporis diffusum in a Spanish patient with aspartylglucosaminuria.Combination therapies for lysosomal storage disease: is the whole greater than the sum of its parts?Lysosomal storage disease: gene therapy on both sides of the blood-brain barrier.Possible role of autoantibodies in the pathophysiology of GM2 gangliosidoses.Hematopoietic cell transplantation for inherited metabolic diseases: an overview of outcomes and practice guidelines.Fast urinary screening of oligosaccharidoses by MALDI-TOF/TOF mass spectrometry.Gene therapy of metachromatic leukodystrophy reverses neurological damage and deficits in mice.Disease specific therapies in leukodystrophies and leukoencephalopathies.Long-term outcomes after allogeneic hematopoietic stem cell transplantation for metachromatic leukodystrophy: the largest single-institution cohort report.White matter dementia.Neuropsychological symptoms of juvenile-onset batten disease: experiences from 2 studies Determinants of health care use in a population-based leukodystrophy cohort.A Prospective Natural History Study of Mucopolysaccharidosis Type IIIA.Juvenile metachromatic leukodystrophy: understanding the disease and implications for nursing care.Novel candidate disease for gene therapy: metachromatic leukodystrophy.A counterintuitive approach to treat enzyme deficiencies: use of enzyme inhibitors for restoring mutant enzyme activity.Emerging trends in transplantation of inherited metabolic diseases.Human CD34+ cells differentiate into microglia and express recombinant therapeutic protein Methods for assessing neurodevelopment in lysosomal storage diseases and related disorders: a multidisciplinary perspective.In utero transplantation of monocytic cells in cats with alpha-mannosidosis.Enzyme therapy for the treatment of type 1 Gaucher disease: clinical outcomes and dose - response relationships.Lysosomal lipid storage diseases.Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.Biotechnological and biomedical applications of mesenchymal stem cells as a therapeutic system.Emerging treatments for pediatric leukodystrophies.Implications of mesenchymal stem cells in regenerative medicine.Combination Therapies for Lysosomal Storage Diseases: A Complex Answer to a Simple Problem.Transplantation in inborn errors of metabolism: current considerations and future perspectives.alpha-L-iduronidase therapy for mucopolysaccharidosis type I.

P2860

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P2860

Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and S

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http://www.wikidata.org/entity/Q33607275

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1999 nî lūn-bûn

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1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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1999 թվականի ապրիլին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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