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T Clayton

Showing results (111-120 of 248) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1992
Liver transplantation in tyrosinaemia type 1: the dilemma of timing the operationA Salt, N D Barnes, K Rolles, et al.
Molecular Genetics and Metabolism|March 12, 2008
Transaldolase deficiency in a two-year-old boy with cirrhosisMirjam M Wamelink, Eduard A Struys, Gajja S Salomons, et al.
Glycobiology|March 11, 2003
The underglycosylation of plasma alpha 1-antitrypsin in congenital disorders of glycosylation type I is not randomKevin Mills, Philippa B Mills, Peter T Clayton, et al.
Neurology|March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiencyK Hyland, I Smith, T Bottiglieri, et al.
Archives of Disease in Childhood|September 1, 1991
Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndromeS P Horslen, P T Clayton, B N Harding, et al.
Archives of Disease in Childhood|August 1, 1996
Evaluation of fasts for investigating hypoglycaemia or suspected metabolic diseaseA A Morris, A Thekekara, Z Wilks, et al.
Journal of Medical Genetics|November 1, 1994
Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophyL C Wilson, M E Oude Luttikhuis, P T Clayton, et al.
Ophthalmology|July 15, 1998
Alström syndrome. Report of 22 cases and literature reviewI M Russell-Eggitt, P T Clayton, R Coffey, et al.
Clinical Chemistry|October 24, 2001
Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technologyK Mills, P B Mills, P T Clayton, et al.
Free Radical Biology & Medicine|September 5, 2002
Synthesis and analysis of conjugates of the major vitamin E metabolite, alpha-CEHCSimon A S Pope, Guillaume E Burtin, Peter T Clayton, et al.
Pageof 25

Showing results (111-120 of 248) with videos related to

Sort By:
Pageof 25
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1992
Liver transplantation in tyrosinaemia type 1: the dilemma of timing the operationA Salt, N D Barnes, K Rolles, et al.
Molecular Genetics and Metabolism|March 12, 2008
Transaldolase deficiency in a two-year-old boy with cirrhosisMirjam M Wamelink, Eduard A Struys, Gajja S Salomons, et al.
Glycobiology|March 11, 2003
The underglycosylation of plasma alpha 1-antitrypsin in congenital disorders of glycosylation type I is not randomKevin Mills, Philippa B Mills, Peter T Clayton, et al.
Neurology|March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiencyK Hyland, I Smith, T Bottiglieri, et al.
Archives of Disease in Childhood|September 1, 1991
Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndromeS P Horslen, P T Clayton, B N Harding, et al.
Archives of Disease in Childhood|August 1, 1996
Evaluation of fasts for investigating hypoglycaemia or suspected metabolic diseaseA A Morris, A Thekekara, Z Wilks, et al.
Journal of Medical Genetics|November 1, 1994
Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophyL C Wilson, M E Oude Luttikhuis, P T Clayton, et al.
Ophthalmology|July 15, 1998
Alström syndrome. Report of 22 cases and literature reviewI M Russell-Eggitt, P T Clayton, R Coffey, et al.
Clinical Chemistry|October 24, 2001
Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technologyK Mills, P B Mills, P T Clayton, et al.
Free Radical Biology & Medicine|September 5, 2002
Synthesis and analysis of conjugates of the major vitamin E metabolite, alpha-CEHCSimon A S Pope, Guillaume E Burtin, Peter T Clayton, et al.
Pageof 25