Neonatal bone marrow transplantation prevents bone pathology in a mouse model of mucopolysaccharidosis type I. - Wikidata - awgldk - TriplyDB

Neonatal bone marrow transplantation prevents bone pathology in a mouse model of mucopolysaccharidosis type I.

Neonatal bone marrow transplantation prevents bone pathology in a mouse model of mucopolysaccharidosis type I.

http://www.wikidata.org/entity/Q35153234

about

Therapies for the bone in mucopolysaccharidoses Characterization of the MPS I-H knock-in mouse reveals increased femoral biomechanical integrity with compromised material strength and altered bone geometry Open issues in Mucopolysaccharidosis type I-Hurler Newborn screening and diagnosis of mucopolysaccharidoses: application of tandem mass spectrometry.Impact of enzyme replacement therapy and hematopoietic stem cell transplantation in patients with Morquio A syndrome.Delayed hypertrophic differentiation of epiphyseal chondrocytes contributes to failed secondary ossification in mucopolysaccharidosis VII dogs Enzymatic replacement therapy for Hunter disease: Up to 9 years experience with 17 patients.Neonatal cellular and gene therapies for mucopolysaccharidoses: the earlier the better?Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC.Pathogenesis and treatment of spine disease in the mucopolysaccharidoses.Neonatal umbilical cord blood transplantation halts skeletal disease progression in the murine model of MPS-I.Impaired bone remodeling and its correction by combination therapy in a mouse model of mucopolysaccharidosis-I.Long-term outcomes of systemic therapies for Hurler syndrome: an international multicenter comparison.

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P2860

Neonatal bone marrow transplantation prevents bone pathology in a mouse model of mucopolysaccharidosis type I.

http://www.wikidata.org/entity/Q35153234

description

2014 nî lūn-bûn

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2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Neonatal bone marrow transplan ...... mucopolysaccharidosis type I.

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Neonatal bone marrow transplan ...... mucopolysaccharidosis type I.

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Neonatal bone marrow transplan ...... mucopolysaccharidosis type I.

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Neonatal bone marrow transplan ...... f mucopolysaccharidosis type I

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Alice Pievani

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Andrea Biondi

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Benedetta Rambaldi

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Cristina Remoli

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Laura Antolini

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Mara Riminucci

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Maria Grazia Valsecchi

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Shunji Tomatsu

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Tsutomu Shimada

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P2860

Orthopaedic management of Hurler's disease after hematopoietic stem cell transplantation: a systematic review.

Murine mucopolysaccharidosis type I: targeted disruption of the murine alpha-L-iduronidase gene

Long-term amelioration of feline Mucopolysaccharidosis VI after AAV-mediated liver gene transfer

Replacing the enzyme alpha-L-iduronidase at birth ameliorates symptoms in the brain and periphery of dogs with mucopolysaccharidosis type I.

Gene therapy augments the efficacy of hematopoietic cell transplantation and fully corrects mucopolysaccharidosis type I phenotype in the mouse model.

Assay for Glycosaminoglycans by Tandem Mass Spectrometry and its Applications.

Detection of inborn errors of metabolism in the newborn.

Cord-blood transplants from unrelated donors in patients with Hurler's syndrome.

Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioning.

Long-term effects of bone marrow transplantation in dogs with mucopolysaccharidosis I.

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1662-1671

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