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P T Clayton

Showing results (61-70 of 101) 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.
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.
BMJ (Clinical Research Ed.)|August 24, 1999
Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometryI Mushtaq, S Logan, M Morris, et al.
The Journal of Clinical Investigation|December 1, 1990
Lack of 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase in fibroblasts from a child with urinary excretion of 3 beta-hydroxy-delta 5-bile acids. A new inborn error of metabolismM S Buchmann, E A Kvittingen, H Nazer, et al.
Archives of Disease in Childhood|May 25, 2004
The significance of a high plasma ammonia valueS L Chow, V Gandhi, S Krywawych, et al.
Pageof 11

Showing results (61-70 of 101) with videos related to

Sort By:
Pageof 11
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.
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.
BMJ (Clinical Research Ed.)|August 24, 1999
Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometryI Mushtaq, S Logan, M Morris, et al.
The Journal of Clinical Investigation|December 1, 1990
Lack of 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase in fibroblasts from a child with urinary excretion of 3 beta-hydroxy-delta 5-bile acids. A new inborn error of metabolismM S Buchmann, E A Kvittingen, H Nazer, et al.
Archives of Disease in Childhood|May 25, 2004
The significance of a high plasma ammonia valueS L Chow, V Gandhi, S Krywawych, et al.
Pageof 11