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Acta Paediatrica (Oslo, Norway : 1992)
|
May 1, 1992
Liver transplantation in tyrosinaemia type 1: the dilemma of timing the operation
A Salt, N D Barnes, K Rolles, et al.
Molecular Genetics and Metabolism
|
March 12, 2008
Transaldolase deficiency in a two-year-old boy with cirrhosis
Mirjam 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 random
Kevin Mills, Philippa B Mills, Peter T Clayton, et al.
Neurology
|
March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency
K Hyland, I Smith, T Bottiglieri, et al.
Archives of Disease in Childhood
|
September 1, 1991
Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome
S 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 disease
A 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 osteodystrophy
L C Wilson, M E Oude Luttikhuis, P T Clayton, et al.
Ophthalmology
|
July 15, 1998
Alström syndrome. Report of 22 cases and literature review
I 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 technology
K 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-CEHC
Simon A S Pope, Guillaume E Burtin, Peter T Clayton, et al.
Page
of 25
Search research articles
Search
Showing results (111-120 of 248) with videos related to
Sort By:
Page
of 25
Acta Paediatrica (Oslo, Norway : 1992)
|
May 1, 1992
Liver transplantation in tyrosinaemia type 1: the dilemma of timing the operation
A Salt, N D Barnes, K Rolles, et al.
Molecular Genetics and Metabolism
|
March 12, 2008
Transaldolase deficiency in a two-year-old boy with cirrhosis
Mirjam 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 random
Kevin Mills, Philippa B Mills, Peter T Clayton, et al.
Neurology
|
March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency
K Hyland, I Smith, T Bottiglieri, et al.
Archives of Disease in Childhood
|
September 1, 1991
Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome
S 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 disease
A 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 osteodystrophy
L C Wilson, M E Oude Luttikhuis, P T Clayton, et al.
Ophthalmology
|
July 15, 1998
Alström syndrome. Report of 22 cases and literature review
I 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 technology
K 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-CEHC
Simon A S Pope, Guillaume E Burtin, Peter T Clayton, et al.
Page
of 25