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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 considerations
I B Sardharwalla, J E Wraith
Journal of Medical Genetics
|
July 1, 1992
A terminal deletion of 11q
C 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 fetus
A 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 patient
R L Soutar, J Mercer, J E Wraith
Journal of Inherited Metabolic Disease
|
January 1, 1996
Mucopolysaccharidosis type IVA (Morquio syndrome): a clinical review
H Northover, R A Cowie, J E Wraith
Clinical Genetics
|
November 15, 2002
Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing clinicians
J 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 newborn
A 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 I
A T Anbu, J Mercer, J E Wraith
Australian Paediatric Journal
|
December 1, 1987
The mucopolysaccharidoses
J E Wraith, J G Rogers, D M Danks
Page
of 12
Search research articles
Search
Showing results (21-30 of 115) with videos related to
Sort By:
Page
of 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 considerations
I B Sardharwalla, J E Wraith
Journal of Medical Genetics
|
July 1, 1992
A terminal deletion of 11q
C 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 fetus
A 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 patient
R L Soutar, J Mercer, J E Wraith
Journal of Inherited Metabolic Disease
|
January 1, 1996
Mucopolysaccharidosis type IVA (Morquio syndrome): a clinical review
H Northover, R A Cowie, J E Wraith
Clinical Genetics
|
November 15, 2002
Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing clinicians
J 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 newborn
A 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 I
A T Anbu, J Mercer, J E Wraith
Australian Paediatric Journal
|
December 1, 1987
The mucopolysaccharidoses
J E Wraith, J G Rogers, D M Danks
Page
of 12