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Publications by Bryan M Turner
Arylsulfatase B Deficiency in Maroteaux-Lamy Syndrome: Cellular Studies and Carrier Identification
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) Gene
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Mitral Stenosis in the Maroteaux-Lamy Syndrome: A Treatable Cause of Dyspnoea.
Postgraduate Medical Journal
Medicine
Clinical and Morphological Features Including Expression of Betaig-H3 and Keratan Sulphate Proteoglycans in Maroteaux-Lamy Syndrome Type B and in Normal Cornea
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Diagnosis of Maroteaux—Lamy Syndrome by the Use of Radiolabelled Oligosaccharides as Substrates for the Determination of Arylsulphatase B Activity
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Sensory-Motor Behavioral Characterization of an Animal Model of Maroteaux-Lamy Syndrome (Or Mucopolysaccharidosis VI)
Scientific Reports
Multidisciplinary
Bisphosphonates and MeCP2 Deficiency: Cellular Studies and Clinical Application in Rett Syndrome
Journal of Musculoskeletal Disorders and Treatment
HumanN-acetylgalactosamine-4-sulphatase Biosynthesis and Maturation in Normal, Maroteaux-Lamy and Multiple-Sulphatase-Deficient Fibroblasts
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Allogeneic CD34 Selected Peripheral Stem Cell Transplant for Maroteaux–Lamy Syndrome (Mucopolysaccharidosis Type VI): Rapid Haemopoietic and Biochemical Reconstitution
Bone Marrow Transplantation
Transplantation
Hematology
Lysosomal Arylsulfatase Deficiencies in Humans: Chromosome Assignments for Arylsulfatase a and B
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
