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Diabetologia
|
October 1, 1992
Increases in plasma lysosomal enzymes in type 1 (insulin-dependent) diabetes mellitus: relationship to diabetic complications and glycaemic control
P J Waters, M D Flynn, R J Corrall, et al.
Biochemical Society Transactions
|
November 1, 1992
Factors affecting the assay of urinary free and bound sialic acid
P J Waters, E M Lewry, A P Brimble, et al.
Molecular Genetics and Metabolism
|
March 18, 2000
Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotype
P J Waters, M A Parniak, B R Akerman, et al.
Biochemical Society Transactions
|
May 1, 1993
Diabetes-related changes in sialic acid content of leucocytes: an assay-dependent artefact?
P J Waters, M D Flynn, C A Pennock, et al.
American Journal of Human Genetics
|
December 18, 1997
Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlations
E Kayaalp, E Treacy, P J Waters, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: a mechanism underlying phenylketonuria
P J Waters, M A Parniak, B R Akerman, et al.
Neuropediatrics
|
November 11, 2008
Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRI
N Brunetti-Pierri, K Selby, M O'Sullivan, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
August 1, 1995
Decreased sialidase activity in mononuclear leucocytes of type 1 diabetic subjects: relationship to diabetic complications and glycaemic control
P J Waters, M D Flynn, C A Pennock, et al.
Neuropediatrics
|
July 4, 2007
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathy
S N Basheer, P J Waters, C W Lam, et al.
Pediatric Research
|
October 6, 1997
Analysis of phenylalanine hydroxylase genotypes and hyperphenylalaninemia phenotypes using L-[1-13C]phenylalanine oxidation rates in vivo: a pilot study
E P Treacy, J J Delente, G Elkas, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Diabetologia
|
October 1, 1992
Increases in plasma lysosomal enzymes in type 1 (insulin-dependent) diabetes mellitus: relationship to diabetic complications and glycaemic control
P J Waters, M D Flynn, R J Corrall, et al.
Biochemical Society Transactions
|
November 1, 1992
Factors affecting the assay of urinary free and bound sialic acid
P J Waters, E M Lewry, A P Brimble, et al.
Molecular Genetics and Metabolism
|
March 18, 2000
Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotype
P J Waters, M A Parniak, B R Akerman, et al.
Biochemical Society Transactions
|
May 1, 1993
Diabetes-related changes in sialic acid content of leucocytes: an assay-dependent artefact?
P J Waters, M D Flynn, C A Pennock, et al.
American Journal of Human Genetics
|
December 18, 1997
Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlations
E Kayaalp, E Treacy, P J Waters, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: a mechanism underlying phenylketonuria
P J Waters, M A Parniak, B R Akerman, et al.
Neuropediatrics
|
November 11, 2008
Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRI
N Brunetti-Pierri, K Selby, M O'Sullivan, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
August 1, 1995
Decreased sialidase activity in mononuclear leucocytes of type 1 diabetic subjects: relationship to diabetic complications and glycaemic control
P J Waters, M D Flynn, C A Pennock, et al.
Neuropediatrics
|
July 4, 2007
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathy
S N Basheer, P J Waters, C W Lam, et al.
Pediatric Research
|
October 6, 1997
Analysis of phenylalanine hydroxylase genotypes and hyperphenylalaninemia phenotypes using L-[1-13C]phenylalanine oxidation rates in vivo: a pilot study
E P Treacy, J J Delente, G Elkas, et al.
Page
of 3