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

Bone marrow transplantation (Basingstoke), 2002-08, Vol.30 (4), p.215-222

2002

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Analysis of factors affecting development of carpal tunnel syndrome in patients with Hurler syndrome after hematopoietic cell transplantation

Bone marrow transplantation (Basingstoke), 2007-03, Vol.39 (6), p.331-334

2007

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Wolman disease successfully treated by bone marrow transplantation

Bone marrow transplantation (Basingstoke), 2000-09, Vol.26 (5), p.567-570

2000

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Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome)

Bone marrow transplantation (Basingstoke), 2000-05, Vol.25 (10), p.1097-1099

2000

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Continued neurocognitive development and prevention of cardiopulmonary complications after successful BMT for I-cell disease: a long-term follow-up report

Bone marrow transplantation (Basingstoke), 2003-11, Vol.32 (9), p.957-960

2003

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Outcome of second hematopoietic cell transplantation in Hurler syndrome

Bone marrow transplantation (Basingstoke), 2002-03, Vol.29 (6), p.491-496

2002

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Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome); an ethical commentary

Bone marrow transplantation (Basingstoke), 2000-05, Vol.25 (10), p.1097-1099

2000

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Oral busulfan pharmacokinetics and engraftment in children with Hurler syndrome and other inherited metabolic storage diseases undergoing hematopoietic cell transplantation

Bone marrow transplantation (Basingstoke), 2001-04, Vol.27 (8), p.855-861

2001

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Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: alpha-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy)

Bone marrow transplantation (Basingstoke), 2000-03, Vol.25 (5), p.541-544

2000

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Wolman's disease: a review of treatment with bone marrow transplantation and considerations for the future

Bone marrow transplantation (Basingstoke), 1992, Vol.10 Suppl 1, p.97

1992

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State of the art review. Bone marrow transplantation treatment for storage diseases. Keystone. January 23, 1992

Bone marrow transplantation (Basingstoke), 1992, Vol.10 Suppl 1, p.87

1992

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Pathology of the liver in mucopolysaccharidosis: light and electron microscopic assessment before and after bone marrow transplantation

Bone marrow transplantation (Basingstoke), 1992-09, Vol.10 (3), p.273

1992

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Allogeneic bone marrow transplantation for Niemann-Pick disease (type IA)

Bone marrow transplantation (Basingstoke), 1992, Vol.10 Suppl 1, p.85

1992

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

Bone marrow transplantation (Basingstoke), 2002, Vol.30 (4), p.215-222

2002

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Outcome of second hematopoietic cell transplantation in Hurler syndrome

Bone marrow transplantation (Basingstoke), 2002-03, Vol.29 (6), p.491-496

2002

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Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: [alpha]-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy)

Bone marrow transplantation (Basingstoke), 2000-03, Vol.25 (5), p.541

2000

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GRISEOFULVIN THERAPY AS A CAUSE OF LYMPH NODE PROLIFERATION RESEMBLING MALIGNANT HISTIOCYTOSIS

Pediatric research, 1977-04, Vol.11 (4), p.470-470

1977

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Primary and Secondary Bile Acids in Meconium

Pediatric research, 1971-01, Vol.5 (6), p.274-279

1971

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4'-DEMETHYL-EPIPODOPHYLLOTOXIN-β-THENYLIDENE GLUCOSIDE (VM-26)(NSC-122819): A NEW DRUG FOR NEUROBLASTOMA

Pediatric research, 1977-04, Vol.11 (4), p.468-468

1977

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Inheritance of a recombinant HL-A haplotype and genetics of the HL -1 region in man

Nature (London), 1974-04, Vol.248 (5448), p.517-519

1974

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2. Enzyme replacement in Fabry's disease

Pediatric research, 1971-02, Vol.5 (2), p.83-83

1971

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659 HERIDITARY ELLIPTOCYTOSIS, RED CELL FRAGMENTATION, AND DECREASED GLUTATHIONE (GSH)

Pediatric research, 1978-04, Vol.12, p.473-473

1978

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

Analysis of factors affecting development of carpal tunnel syndrome in patients with Hurler syndrome after hematopoietic cell transplantation

Wolman disease successfully treated by bone marrow transplantation

Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome)

Continued neurocognitive development and prevention of cardiopulmonary complications after successful BMT for I-cell disease: a long-term follow-up report

Outcome of second hematopoietic cell transplantation in Hurler syndrome

Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome); an ethical commentary

Oral busulfan pharmacokinetics and engraftment in children with Hurler syndrome and other inherited metabolic storage diseases undergoing hematopoietic cell transplantation

Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: alpha-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy)

Wolman's disease: a review of treatment with bone marrow transplantation and considerations for the future

State of the art review. Bone marrow transplantation treatment for storage diseases. Keystone. January 23, 1992

Pathology of the liver in mucopolysaccharidosis: light and electron microscopic assessment before and after bone marrow transplantation

Allogeneic bone marrow transplantation for Niemann-Pick disease (type IA)

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

Outcome of second hematopoietic cell transplantation in Hurler syndrome

Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: [alpha]-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy)

GRISEOFULVIN THERAPY AS A CAUSE OF LYMPH NODE PROLIFERATION RESEMBLING MALIGNANT HISTIOCYTOSIS

Primary and Secondary Bile Acids in Meconium

4'-DEMETHYL-EPIPODOPHYLLOTOXIN-β-THENYLIDENE GLUCOSIDE (VM-26)(NSC-122819): A NEW DRUG FOR NEUROBLASTOMA

Inheritance of a recombinant HL-A haplotype and genetics of the HL -1 region in man

2. Enzyme replacement in Fabry's disease

659 HERIDITARY ELLIPTOCYTOSIS, RED CELL FRAGMENTATION, AND DECREASED GLUTATHIONE (GSH)

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