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Clinical characterization of cardiovascular abnormalities associated with feline mucopolysaccharidosis I and VI

Journal of inherited metabolic disease, 2008-06, Vol.31 (3), p.424-431

2008

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Gene therapy ameliorates cardiovascular disease in dogs with mucopolysaccharidosis VII

Circulation (New York, N.Y.), 2004-08, Vol.110 (7), p.815-820

2004

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Adeno-associated virus serotypes 9 and rh10 mediate strong neuronal transduction of the dog brain

Gene therapy, 2014-01, Vol.21 (1), p.28-36

2014

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Mucopolysaccharidosis VII in a Cat Caused by 2 Adjacent Missense Mutations in the GUSB Gene

Journal of veterinary internal medicine, 2015-07, Vol.29 (4), p.1022-1028

2015

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A model of mucopolysaccharidosis IIIB (Sanfilippo syndrome type IIIB): N‐acetyl‐α‐D‐glucosaminidase deficiency in Schipperke dogs

Journal of inherited metabolic disease, 2003-01, Vol.26 (5), p.489-504

2003

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Abnormal neuronal metabolism and storage in mucopolysaccharidosis type VI (Maroteaux-Lamy) disease

Neuropathology and applied neurobiology, 2005-10, Vol.31 (5), p.536-544

2005

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Nurse leadership: Sustaining a culture of safety

Health SA = SA Gesondheid, 2022, Vol.27 (1), p.2009-2009

2022

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Enzyme Replacement Therapy in Feline Mucopolysaccharidosis I

Molecular genetics and metabolism, 2001-03, Vol.72 (3), p.199-208

2001

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Inheritance, biochemical abnormalities, and clinical features of feline Mucolipidosis II: the first animal model of human I-cell disease

The Journal of heredity, 2003-09, Vol.94 (5), p.363-373

2003

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Molecular Basis of Feline β-Glucuronidase Deficiency: An Animal Model of Mucopolysaccharidosis VII

Genomics (San Diego, Calif.), 1999-06, Vol.58 (2), p.121-128

1999

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Articular Chondrocytes from Animals with a Dermatan Sulfate Storage Disease Undergo a High Rate of Apoptosis and Release Nitric Oxide and Inflammatory Cytokines: A Possible Mechanism Underlying Degenerative Joint Disease in the Mucopolysaccharidoses

Laboratory investigation, 2001-09, Vol.81 (9), p.1319-1328

2001

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Neonatal Gene Transfer Leads to Widespread Correction of Pathology in a Murine Model of Lysosomal Storage Disease

Proceedings of the National Academy of Sciences - PNAS, 1999-03, Vol.96 (5), p.2296-2300

1999

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Autologous transplantation of retrovirally transduced bone marrow or neonatal blood cells into cats can lead to long-term engraftment in the absence of myeloablation

Gene therapy, 1999, Vol.6 (1), p.107-113

1999

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Cloning of the Canine β-Glucuronidase cDNA, Mutation Identification in Canine MPS VII, and Retroviral Vector-Mediated Correction of MPS VII Cells

Genomics (San Diego, Calif.), 1998-03, Vol.48 (2), p.248-253

1998

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Biochemical, pathological, and clinical response to transplantation of normal bone marrow cells into acid sphingomyelinase-deficient mice

Transplantation, 1998-04, Vol.65 (7), p.884

1998

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Inherited platelet delta-storage pool disease in dogs causing severe bleeding: an animal model for a specific ADP deficiency

Thrombosis and haemostasis, 1995-09, Vol.74 (3), p.949

1995

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MRI and electrophysiological abnormalities in a case of canine globoid cell leucodystrophy

Journal of small animal practice, 1998-08, Vol.39 (8), p.401-405

1998

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Retrovirus vector-mediated correction and cross-correction of lysosomal α-mannosidase deficiency in human and feline fibroblasts

Human gene therapy, 1999-05, Vol.10 (8), p.1311-1319

1999

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Neonatal intramuscular injection with recombinant adeno-associated virus results in prolonged beta-glucuronidase expression in situ and correction of liver pathology in mucopolysaccharidosis type VII mice

Human gene therapy, 1999-01, Vol.10 (1), p.85-94

1999

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Restoration of Normal Lysosomal Function in Mucopolysaccharidosis Type VII Cells by Retroviral Vector-Mediated Gene Transfer

Proceedings of the National Academy of Sciences - PNAS, 1990-04, Vol.87 (8), p.2877-2881

1990

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Biochemical basis of the β-glucuronidase gene defect causing canine mucopolysaccharidosis VII

The Journal of heredity, 1999-01, Vol.90 (1), p.119-123

1999

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Bone marrow transplantation in newborn rats with mucopolysaccharidosis type VI: biochemical, pathological, and clinical findings

Transplantation, 1997-05, Vol.63 (10), p.1386

1997

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Glycogen storage disease type IV : inherited deficiency of branching enzyme activity in cats

Pediatric research, 1992-12, Vol.32 (6), p.719-725

1992

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Mechanism of Glycosaminoglycan-Mediated Bone and Joint Disease: Implications for the Mucopolysaccharidoses and Other Connective Tissue Diseases

The American journal of pathology, 2008-01, Vol.172 (1), p.112-122

2008

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Mucopolysaccharidosis type VII (Sly syndrome) : beta-glucuronidase-deficient mucopolysaccharidosis in the dog

The American journal of pathology, 1991-06, Vol.138 (6), p.1553-1555

1991

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Clinical characterization of cardiovascular abnormalities associated with feline mucopolysaccharidosis I and VI

Gene therapy ameliorates cardiovascular disease in dogs with mucopolysaccharidosis VII

Adeno-associated virus serotypes 9 and rh10 mediate strong neuronal transduction of the dog brain

Mucopolysaccharidosis VII in a Cat Caused by 2 Adjacent Missense Mutations in the GUSB Gene

A model of mucopolysaccharidosis IIIB (Sanfilippo syndrome type IIIB): N‐acetyl‐α‐D‐glucosaminidase deficiency in Schipperke dogs

Abnormal neuronal metabolism and storage in mucopolysaccharidosis type VI (Maroteaux-Lamy) disease

Nurse leadership: Sustaining a culture of safety

Enzyme Replacement Therapy in Feline Mucopolysaccharidosis I

Inheritance, biochemical abnormalities, and clinical features of feline Mucolipidosis II: the first animal model of human I-cell disease

Molecular Basis of Feline β-Glucuronidase Deficiency: An Animal Model of Mucopolysaccharidosis VII

Articular Chondrocytes from Animals with a Dermatan Sulfate Storage Disease Undergo a High Rate of Apoptosis and Release Nitric Oxide and Inflammatory Cytokines: A Possible Mechanism Underlying Degenerative Joint Disease in the Mucopolysaccharidoses

Neonatal Gene Transfer Leads to Widespread Correction of Pathology in a Murine Model of Lysosomal Storage Disease

Autologous transplantation of retrovirally transduced bone marrow or neonatal blood cells into cats can lead to long-term engraftment in the absence of myeloablation

Cloning of the Canine β-Glucuronidase cDNA, Mutation Identification in Canine MPS VII, and Retroviral Vector-Mediated Correction of MPS VII Cells

Biochemical, pathological, and clinical response to transplantation of normal bone marrow cells into acid sphingomyelinase-deficient mice

Inherited platelet delta-storage pool disease in dogs causing severe bleeding: an animal model for a specific ADP deficiency

MRI and electrophysiological abnormalities in a case of canine globoid cell leucodystrophy

Retrovirus vector-mediated correction and cross-correction of lysosomal α-mannosidase deficiency in human and feline fibroblasts

Neonatal intramuscular injection with recombinant adeno-associated virus results in prolonged beta-glucuronidase expression in situ and correction of liver pathology in mucopolysaccharidosis type VII mice

Restoration of Normal Lysosomal Function in Mucopolysaccharidosis Type VII Cells by Retroviral Vector-Mediated Gene Transfer

Biochemical basis of the β-glucuronidase gene defect causing canine mucopolysaccharidosis VII

Bone marrow transplantation in newborn rats with mucopolysaccharidosis type VI: biochemical, pathological, and clinical findings

Glycogen storage disease type IV : inherited deficiency of branching enzyme activity in cats

Mechanism of Glycosaminoglycan-Mediated Bone and Joint Disease: Implications for the Mucopolysaccharidoses and Other Connective Tissue Diseases

Mucopolysaccharidosis type VII (Sly syndrome) : beta-glucuronidase-deficient mucopolysaccharidosis in the dog

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