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Annals of Clinical Biochemistry
|
March 1, 1994
Quality assessment of urinary organic acid analysis
J R Bonham, M Downing, R J Pollitt, et al.
The Analyst
|
February 25, 1998
Determination of antimony in urine, blood and serum and in liver and lung tissues of infants by inductively coupled plasma mass spectrometry
H T Delves, C E Sieniawska, G S Fell, et al.
Brain & Development
|
January 1, 1990
Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome
A Clarke, D Gardner-Medwin, J Richardson, et al.
Journal of Inherited Metabolic Disease
|
March 10, 1999
Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type II
N J Manning, J R Bonham, M Downing, et al.
Journal of Inherited Metabolic Disease
|
July 18, 2002
Vitamin C therapy ameliorates vascular endothelial dysfunction in treated patients with homocystinuria
C H Pullin, J R Bonham, I F W McDowell, et al.
Journal of Neurochemistry
|
March 1, 1988
Muscarinic cholinergic receptor subtypes in hippocampus in human cognitive disorders
C J Smith, E K Perry, R H Perry, et al.
Journal of Inherited Metabolic Disease
|
May 11, 1999
The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease
J R Bonham, P Guthrie, M Downing, et al.
Journal of Inherited Metabolic Disease
|
April 5, 2001
Features of carnitine palmitoyltransferase type I deficiency
S E Olpin, J Allen, J R Bonham, et al.
Journal of Inherited Metabolic Disease
|
May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency
S E Olpin, S Clark, B S Andresen, et al.
Journal of Inherited Metabolic Disease
|
November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency
S E Olpin, A Afifi, S Clark, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 60) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 60 results.
Annals of Clinical Biochemistry
|
March 1, 1994
Quality assessment of urinary organic acid analysis
J R Bonham, M Downing, R J Pollitt, et al.
The Analyst
|
February 25, 1998
Determination of antimony in urine, blood and serum and in liver and lung tissues of infants by inductively coupled plasma mass spectrometry
H T Delves, C E Sieniawska, G S Fell, et al.
Brain & Development
|
January 1, 1990
Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome
A Clarke, D Gardner-Medwin, J Richardson, et al.
Journal of Inherited Metabolic Disease
|
March 10, 1999
Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type II
N J Manning, J R Bonham, M Downing, et al.
Journal of Inherited Metabolic Disease
|
July 18, 2002
Vitamin C therapy ameliorates vascular endothelial dysfunction in treated patients with homocystinuria
C H Pullin, J R Bonham, I F W McDowell, et al.
Journal of Neurochemistry
|
March 1, 1988
Muscarinic cholinergic receptor subtypes in hippocampus in human cognitive disorders
C J Smith, E K Perry, R H Perry, et al.
Journal of Inherited Metabolic Disease
|
May 11, 1999
The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease
J R Bonham, P Guthrie, M Downing, et al.
Journal of Inherited Metabolic Disease
|
April 5, 2001
Features of carnitine palmitoyltransferase type I deficiency
S E Olpin, J Allen, J R Bonham, et al.
Journal of Inherited Metabolic Disease
|
May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency
S E Olpin, S Clark, B S Andresen, et al.
Journal of Inherited Metabolic Disease
|
November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency
S E Olpin, A Afifi, S Clark, et al.
Page
of 6