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G Rylance

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

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Archives of Disease in Childhood|May 1, 1996
Factors affecting the variation in plasma phenylalanine in patients with phenylketonuria on dietA MacDonald, G Rylance, S K Hall, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Administration of protein substitute and quality of control in phenylketonuria: a randomized studyA MacDonald, G Rylance, P Davies, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Free use of fruits and vegetables in phenylketonuriaA MacDonald, G Rylance, P Davies, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiencyK L Chambliss, R G Gray, G Rylance, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 30, 2004
How do paediatricians communicate with children and parents?E Wassmer, G Minnaar, N Abdel Aal, et al.
Journal of Inherited Metabolic Disease|June 11, 2004
Protein substitutes for PKU: what's new?A Macdonald, A Daly, P Davies, et al.
Archives of Disease in Childhood|March 26, 2003
Are tablets a practical source of protein substitute in phenylketonuria?A MacDonald, C Ferguson, G Rylance, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Biochemical monitoring of treatment for galactosaemia: biological variability in metabolite concentrationsA C Hutchesson, C Murdoch-Davis, A Green, et al.
Lancet (London, England)|September 8, 1990
Neurological deterioration in young adults with phenylketonuriaA J Thompson, I Smith, D Brenton, et al.
Lancet (London, England)|July 13, 2002
How practical are recommendations for dietary control in phenylketonuria?J H Walter, F J White, S K Hall, et al.
Pageof 4

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

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Archives of Disease in Childhood|May 1, 1996
Factors affecting the variation in plasma phenylalanine in patients with phenylketonuria on dietA MacDonald, G Rylance, S K Hall, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Administration of protein substitute and quality of control in phenylketonuria: a randomized studyA MacDonald, G Rylance, P Davies, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Free use of fruits and vegetables in phenylketonuriaA MacDonald, G Rylance, P Davies, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiencyK L Chambliss, R G Gray, G Rylance, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 30, 2004
How do paediatricians communicate with children and parents?E Wassmer, G Minnaar, N Abdel Aal, et al.
Journal of Inherited Metabolic Disease|June 11, 2004
Protein substitutes for PKU: what's new?A Macdonald, A Daly, P Davies, et al.
Archives of Disease in Childhood|March 26, 2003
Are tablets a practical source of protein substitute in phenylketonuria?A MacDonald, C Ferguson, G Rylance, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Biochemical monitoring of treatment for galactosaemia: biological variability in metabolite concentrationsA C Hutchesson, C Murdoch-Davis, A Green, et al.
Lancet (London, England)|September 8, 1990
Neurological deterioration in young adults with phenylketonuriaA J Thompson, I Smith, D Brenton, et al.
Lancet (London, England)|July 13, 2002
How practical are recommendations for dietary control in phenylketonuria?J H Walter, F J White, S K Hall, et al.
Pageof 4