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J E Wraith

Showing results (31-40 of 115) with videos related to

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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 1, 1997
Cervical decompression in mild mucopolysaccharidosis type II (Hunter syndrome)D P O'Brien, R A Cowie, J E Wraith
Journal of Inherited Metabolic Disease|January 27, 2005
Pregnancy in a patient with mucopolysaccharidosis type IH homozygous for the W402X mutationC J Hendriksz, G M Moss, J E Wraith
Pediatric Research|January 1, 1997
Methionine and serine formation in control and mutant human cultured fibroblasts: evidence for methyl trapping and characterization of remethylation defectsB Fowler, C Whitehouse, F Wenzel, et al.
Clinical Radiology|October 1, 1996
Magnetic resonance imaging of the brain, neck and cervical spine in mild Hunter's syndrome (mucopolysaccharidoses type II)V J Parsons, D G Hughes, J E Wraith
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 1, 1995
Absence of acidosis in the initial presentation of propionic acidaemiaJ H Walter, J E Wraith, M A Cleary
The Medical Journal of Australia|November 2, 1987
Mild Sanfilippo syndrome: a further cause of hyperactivity and behavioural disturbanceJ E Wraith, D M Danks, J G Rogers
Anaesthesia|December 1, 1994
Anaesthesia and mucopolysaccharidoses. A review of airway problems in childrenR W Walker, M Darowski, P Morris, et al.
Journal of Inherited Metabolic Disease|April 23, 2003
Second case of a successful pregnancy in maternal isovaleric acidaemiaS Spinty, H Rogozinski, G T Lealman, et al.
Ophthalmic Genetics|October 18, 2000
Optic atrophy in association with cobalamin C (cblC) diseaseN Patton, S Beatty, I C Lloyd, et al.
Archives of Disease in Childhood|July 1, 1997
Mutation analysis in 46 British and Irish patients with Gaucher's diseaseC E Hatton, A Cooper, C Whitehouse, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 1, 1997
Cervical decompression in mild mucopolysaccharidosis type II (Hunter syndrome)D P O'Brien, R A Cowie, J E Wraith
Journal of Inherited Metabolic Disease|January 27, 2005
Pregnancy in a patient with mucopolysaccharidosis type IH homozygous for the W402X mutationC J Hendriksz, G M Moss, J E Wraith
Pediatric Research|January 1, 1997
Methionine and serine formation in control and mutant human cultured fibroblasts: evidence for methyl trapping and characterization of remethylation defectsB Fowler, C Whitehouse, F Wenzel, et al.
Clinical Radiology|October 1, 1996
Magnetic resonance imaging of the brain, neck and cervical spine in mild Hunter's syndrome (mucopolysaccharidoses type II)V J Parsons, D G Hughes, J E Wraith
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 1, 1995
Absence of acidosis in the initial presentation of propionic acidaemiaJ H Walter, J E Wraith, M A Cleary
The Medical Journal of Australia|November 2, 1987
Mild Sanfilippo syndrome: a further cause of hyperactivity and behavioural disturbanceJ E Wraith, D M Danks, J G Rogers
Anaesthesia|December 1, 1994
Anaesthesia and mucopolysaccharidoses. A review of airway problems in childrenR W Walker, M Darowski, P Morris, et al.
Journal of Inherited Metabolic Disease|April 23, 2003
Second case of a successful pregnancy in maternal isovaleric acidaemiaS Spinty, H Rogozinski, G T Lealman, et al.
Ophthalmic Genetics|October 18, 2000
Optic atrophy in association with cobalamin C (cblC) diseaseN Patton, S Beatty, I C Lloyd, et al.
Archives of Disease in Childhood|July 1, 1997
Mutation analysis in 46 British and Irish patients with Gaucher's diseaseC E Hatton, A Cooper, C Whitehouse, et al.
Pageof 12