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J E Wraith

Showing results (61-70 of 115) with videos related to

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American Journal of Medical Genetics|February 1, 1990
Geleophysic dysplasiaJ E Wraith, A Bankier, C W Chow, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Complete reversal of moderate/severe brain MRI abnormalities in a patient with classical phenylketonuriaJ H Walter, F White, J E Wraith, et al.
Archives of Disease in Childhood|January 6, 1999
Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease)E Vafiadaki, A Cooper, L E Heptinstall, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 31, 2002
Cardiovascular changes in children with mucopolysaccharide disordersU R Mohan, A A Hay, M A Cleary, et al.
European Journal of Pediatrics|October 1, 1988
Maternal phenylketonuria: successful outcome in four pregnancies treated prior to conceptionB C Lynch, D B Pitt, T G Maddison, et al.
European Journal of Pediatrics|September 1, 1987
Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduriaE A Haan, R D Scholem, J J Pitt, et al.
Neuroradiology|May 1, 1997
MRI of the brain and craniocervical junction in Morquio's diseaseD G Hughes, R D Chadderton, R A Cowie, et al.
Neurology|February 1, 1989
Sulfite oxidase deficiency: clinical, neuroradiologic, and biochemical features in two new patientsG K Brown, R D Scholem, H B Croll, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutationA Chakrapani, S Olpin, M Cleary, et al.
Molecular Genetics and Metabolism|December 11, 2012
Developmental outcome post allogenic bone marrow transplant for Niemann Pick Type C2C Breen, R F Wynn, A O'Meara, et al.
Pageof 12

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|February 1, 1990
Geleophysic dysplasiaJ E Wraith, A Bankier, C W Chow, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Complete reversal of moderate/severe brain MRI abnormalities in a patient with classical phenylketonuriaJ H Walter, F White, J E Wraith, et al.
Archives of Disease in Childhood|January 6, 1999
Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease)E Vafiadaki, A Cooper, L E Heptinstall, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 31, 2002
Cardiovascular changes in children with mucopolysaccharide disordersU R Mohan, A A Hay, M A Cleary, et al.
European Journal of Pediatrics|October 1, 1988
Maternal phenylketonuria: successful outcome in four pregnancies treated prior to conceptionB C Lynch, D B Pitt, T G Maddison, et al.
European Journal of Pediatrics|September 1, 1987
Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduriaE A Haan, R D Scholem, J J Pitt, et al.
Neuroradiology|May 1, 1997
MRI of the brain and craniocervical junction in Morquio's diseaseD G Hughes, R D Chadderton, R A Cowie, et al.
Neurology|February 1, 1989
Sulfite oxidase deficiency: clinical, neuroradiologic, and biochemical features in two new patientsG K Brown, R D Scholem, H B Croll, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutationA Chakrapani, S Olpin, M Cleary, et al.
Molecular Genetics and Metabolism|December 11, 2012
Developmental outcome post allogenic bone marrow transplant for Niemann Pick Type C2C Breen, R F Wynn, A O'Meara, et al.
Pageof 12