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J E Wraith

Showing results (51-60 of 115) with videos related to

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Archives of Disease in Childhood|April 1, 1996
Histidinaemia: a benign metabolic disorderW K Lam, M A Cleary, J E Wraith, et al.
Archives of Disease in Childhood|September 1, 1991
No sensory neuropathy during pyridoxine treatment in homocystinuriaC Mpofu, S M Alani, C Whitehouse, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
beta-mannosidase deficiency in a female infant with epileptic encephalopathyA Cooper, J E Wraith, W J Savage, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
A patient with severe type of epimerase deficiency galactosaemiaI B Sardharwalla, J E Wraith, C Bridge, et al.
Journal of Inherited Metabolic Disease|October 17, 2008
Home treatment with Elaprase and Naglazyme is safe in patients with mucopolysaccharidoses types II and VI, respectivelyS Bagewadi, J Roberts, J Mercer, et al.
Clinical Genetics|May 11, 2007
Newborn screening for mucopolysaccharidoses: opinions of patients and their familiesI M Hayes, V Collins, M Sahhar, et al.
Journal of Inherited Metabolic Disease|October 28, 2010
Effects of enzyme replacement therapy on growth in patients with mucopolysaccharidosis type IIG Schulze-Frenking, Simon A Jones, J Roberts, et al.
European Journal of Pediatrics|May 20, 1998
Strategies for the treatment of cystathionine beta-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 yearsJ H Walter, J E Wraith, F J White, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Long-term follow-up following bone marrow transplantation for Hunter diseaseA Vellodi, E Young, A Cooper, et al.
The Journal of Laryngology and Otology|June 21, 2003
Hearing loss due to mannosidosis and otitis media with effusion. A case report and review of audiological assessments in children with otitis media with effusionA U Ahmmed, S M O'Halloran, N J Roland, et al.
Pageof 12

Showing results (51-60 of 115) with videos related to

Sort By:
Pageof 12
Archives of Disease in Childhood|April 1, 1996
Histidinaemia: a benign metabolic disorderW K Lam, M A Cleary, J E Wraith, et al.
Archives of Disease in Childhood|September 1, 1991
No sensory neuropathy during pyridoxine treatment in homocystinuriaC Mpofu, S M Alani, C Whitehouse, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
beta-mannosidase deficiency in a female infant with epileptic encephalopathyA Cooper, J E Wraith, W J Savage, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
A patient with severe type of epimerase deficiency galactosaemiaI B Sardharwalla, J E Wraith, C Bridge, et al.
Journal of Inherited Metabolic Disease|October 17, 2008
Home treatment with Elaprase and Naglazyme is safe in patients with mucopolysaccharidoses types II and VI, respectivelyS Bagewadi, J Roberts, J Mercer, et al.
Clinical Genetics|May 11, 2007
Newborn screening for mucopolysaccharidoses: opinions of patients and their familiesI M Hayes, V Collins, M Sahhar, et al.
Journal of Inherited Metabolic Disease|October 28, 2010
Effects of enzyme replacement therapy on growth in patients with mucopolysaccharidosis type IIG Schulze-Frenking, Simon A Jones, J Roberts, et al.
European Journal of Pediatrics|May 20, 1998
Strategies for the treatment of cystathionine beta-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 yearsJ H Walter, J E Wraith, F J White, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Long-term follow-up following bone marrow transplantation for Hunter diseaseA Vellodi, E Young, A Cooper, et al.
The Journal of Laryngology and Otology|June 21, 2003
Hearing loss due to mannosidosis and otitis media with effusion. A case report and review of audiological assessments in children with otitis media with effusionA U Ahmmed, S M O'Halloran, N J Roland, et al.
Pageof 12