Allogeneic mesenchymal stem cell infusion for treatment of metachromatic leukodystrophy (MLD) and Hurler syndrome (MPS-IH)

Bone Marrow Transplantation

Volumn 30, Issue 4, 2002, Pages 215-222

  Koc O N ^a   Day, J ^b   Nieder, M ^c   Gerson, S L ^a   Lazarus, H M ^a   Krivit, W ^d  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

^c UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^d UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

Hurler; MLD; MSC; Storage disorders; Stromal cell

Indexed keywords

ADOLESCENT; ADULT; ALLOTRANSPLANTATION; ARTICLE; BONE MARROW CELL; BONE MARROW TRANSPLANTATION; CHILD; CLINICAL TRIAL; CULTURE TECHNIQUE; CYTOLOGY; FEMALE; HEMATOPOIETIC STEM CELL TRANSPLANTATION; HISTOCOMPATIBILITY; HUMAN; HURLER SYNDROME; MALE; MESODERM; METACHROMATIC LEUKODYSTROPHY; METHODOLOGY; NERVE CONDUCTION; PRESCHOOL CHILD; TRANSPLANTATION; TREATMENT OUTCOME; BONE DEFECT; BONE DENSITY; BONE MINERAL; CELL CULTURE; CELL ISOLATION; CLINICAL ARTICLE; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HEALTH STATUS; HLA MATCHING; HUMAN CELL; MENTAL DEVELOPMENT; MESENCHYME CELL; NEUROLOGIC DISEASE; PHYSICAL DEVELOPMENT; PRIORITY JOURNAL; SAFETY; SIBLING; SURVIVAL; TOXICITY;

ADOLESCENT; ADULT; BONE MARROW CELLS; BONE MARROW TRANSPLANTATION; CELL CULTURE TECHNIQUES; CHILD; CHILD, PRESCHOOL; FEMALE; HEMATOPOIETIC STEM CELL TRANSPLANTATION; HUMANS; LEUKODYSTROPHY, METACHROMATIC; MALE; MESODERM; MUCOPOLYSACCHARIDOSIS I; NEURAL CONDUCTION; TRANSPLANTATION CHIMERA; TRANSPLANTATION, HOMOLOGOUS; TREATMENT OUTCOME;

EID: 0036676009     PISSN: 02683369     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.bmt.1703650     Document Type: Article

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