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J E Wraith

Showing results (21-30 of 115) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1989
A clinician's view of the mass screening of the newborn for inherited diseases: current practice and future considerationsI B Sardharwalla, J E Wraith
Journal of Medical Genetics|July 1, 1992
A terminal deletion of 11qC Schwarz, C Mpofu, J E Wraith
Prenatal Diagnosis|September 1, 1991
First-trimester diagnosis of Hunter syndrome: very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetusA Cooper, M Thornley, J E Wraith
Journal of Inherited Metabolic Disease|July 11, 2006
Impact of 144 weeks of laronidase therapy on body functions, endurance and general well-being in a Hurler-Scheie patientR L Soutar, J Mercer, J E Wraith
Journal of Inherited Metabolic Disease|January 1, 1996
Mucopolysaccharidosis type IVA (Morquio syndrome): a clinical reviewH Northover, R A Cowie, J E Wraith
Clinical Genetics|November 15, 2002
Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing cliniciansJ Fraser, J E Wraith, M B Delatycki
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 26, 2001
Detection of inborn errors of metabolism in the newbornA Chakrapani, M A Cleary, J E Wraith
Journal of Inherited Metabolic Disease|February 19, 2010
The effects of early and late bone marrow transplantation in siblings with alpha-mannosidosis. Is early haematopoietic cell transplantation the preferred treatment option?A A Broomfield, A Chakrapani, J E Wraith
Journal of Inherited Metabolic Disease|April 8, 2006
Effect of discontinuing of laronidase in a patient with mucopolysaccharidosis type IA T Anbu, J Mercer, J E Wraith
Australian Paediatric Journal|December 1, 1987
The mucopolysaccharidosesJ E Wraith, J G Rogers, D M Danks
Pageof 12

Showing results (21-30 of 115) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|January 1, 1989
A clinician's view of the mass screening of the newborn for inherited diseases: current practice and future considerationsI B Sardharwalla, J E Wraith
Journal of Medical Genetics|July 1, 1992
A terminal deletion of 11qC Schwarz, C Mpofu, J E Wraith
Prenatal Diagnosis|September 1, 1991
First-trimester diagnosis of Hunter syndrome: very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetusA Cooper, M Thornley, J E Wraith
Journal of Inherited Metabolic Disease|July 11, 2006
Impact of 144 weeks of laronidase therapy on body functions, endurance and general well-being in a Hurler-Scheie patientR L Soutar, J Mercer, J E Wraith
Journal of Inherited Metabolic Disease|January 1, 1996
Mucopolysaccharidosis type IVA (Morquio syndrome): a clinical reviewH Northover, R A Cowie, J E Wraith
Clinical Genetics|November 15, 2002
Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing cliniciansJ Fraser, J E Wraith, M B Delatycki
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 26, 2001
Detection of inborn errors of metabolism in the newbornA Chakrapani, M A Cleary, J E Wraith
Journal of Inherited Metabolic Disease|February 19, 2010
The effects of early and late bone marrow transplantation in siblings with alpha-mannosidosis. Is early haematopoietic cell transplantation the preferred treatment option?A A Broomfield, A Chakrapani, J E Wraith
Journal of Inherited Metabolic Disease|April 8, 2006
Effect of discontinuing of laronidase in a patient with mucopolysaccharidosis type IA T Anbu, J Mercer, J E Wraith
Australian Paediatric Journal|December 1, 1987
The mucopolysaccharidosesJ E Wraith, J G Rogers, D M Danks
Pageof 12