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Results of search for 'au:"Coates, P M"', page 4 of 5
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Authors
Adebonojo, F O
Bennett, M J
Brown, S A
Coates, P M
Corkey, B E
Cortner, J A
Cryer, D R
Finegold, D N
Gallagher, P R
Hale, D E
Hayman, L L
Indo, Y
Jarvik, G P
Kelley, R I
Koldovsky, O
Le, N A
Meininger, J C
Rinaldo, P
Stanley, C A
Tanaka, K
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Topics
Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenases
Adult
Carnitine
Child
Child, Preschool
Female
Fibroblasts
Humans
Infant
Lipase
Liver
Male
Mutation
blood
deficiency
diagnosis
enzymology
genetics
metabolism
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English
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61.
Determinants of fasting plasma triglyceride levels: metabolism of hepatic and intestinal lipoproteins.
[electronic resource]
by
Cortner, J A
Le, N A
Coates, P M
Bennett, M J
Cryer, D R
Producer:
19920616
In:
European journal of clinical investigation
vol. 22
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62.
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts.
[electronic resource]
by
Treem, W R
Stanley, C A
Finegold, D N
Hale, D E
Coates, P M
Producer:
19881205
In:
The New England journal of medicine
vol. 319
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63.
Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.
[electronic resource]
by
Coates, P M
Hale, D E
Stanley, C A
Corkey, B E
Cortner, J A
Producer:
19850916
In:
Pediatric research
vol. 19
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64.
Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemia.
[electronic resource]
by
Jarvik, G P
Beaty, T H
Gallagher, P R
Coates, P M
Cortner, J A
Producer:
19931210
In:
Genetic epidemiology
vol. 10
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65.
Direct measurement of apolipoprotein B synthesis in human very low density lipoprotein using stable isotopes and mass spectrometry.
[electronic resource]
by
Cryer, D R
Matsushima, T
Marsh, J B
Yudkoff, M
Coates, P M
Cortner, J A
Producer:
19860916
In:
Journal of lipid research
vol. 27
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66.
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
[electronic resource]
by
Rinaldo, P
O'Shea, J J
Coates, P M
Hale, D E
Stanley, C A
Tanaka, K
Producer:
19881205
In:
The New England journal of medicine
vol. 319
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67.
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels.
[electronic resource]
by
Iolascon, A
Parrella, T
Perrotta, S
Guardamagna, O
Coates, P M
Sartore, M
Surrey, S
Fortina, P
Producer:
19941207
In:
Journal of medical genetics
vol. 31
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68.
Measurement of (C13)arginine incorporation into apolipoprotein B-100 in very low density lipoproteins and low density lipoproteins in normal subjects using (13C)sodium bicarbonate infusion and isotope ratio mass spectrometry.
[electronic resource]
by
Bennett, M J
Cryer, D R
Yudkoff, M
Coates, P M
Cortner, J A
Marsh, J B
Producer:
19901119
In:
Biomedical & environmental mass spectrometry
vol. 19
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69.
Effects of family history of heart disease, apolipoprotein E phenotype, and lipoprotein(a) on the response of children's plasma lipids to change in dietary lipids.
[electronic resource]
by
Dixon, L B
Shannon, B M
Tershakovec, A M
Bennett, M J
Coates, P M
Cortner, J A
Producer:
19971120
In:
The American journal of clinical nutrition
vol. 66
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70.
Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings.
[electronic resource]
by
Catzeflis, C
Bachmann, C
Hale, D E
Coates, P M
Wiesmann, U
Colombo, J P
Joris, F
Délèze, G
Producer:
19900711
In:
European journal of pediatrics
vol. 149
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71.
Kinetics of chylomicron remnant clearance in normal and in hyperlipoproteinemic subjects.
[electronic resource]
by
Cortner, J A
Coates, P M
Le, N A
Cryer, D R
Ragni, M C
Faulkner, A
Langer, T
Producer:
19870528
In:
Journal of lipid research
vol. 28
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72.
Neonatal presentation of I-cell disease.
[electronic resource]
by
Sprigz, R A
Doughty, R A
Spackman, T J
Murane, M J
Coates, P M
Koldovský, O
Zackai, E H
Producer:
19790212
In:
The Journal of pediatrics
vol. 93
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73.
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.
[electronic resource]
by
Hale, D E
Batshaw, M L
Coates, P M
Frerman, F E
Goodman, S I
Singh, I
Stanley, C A
Producer:
19850916
In:
Pediatric research
vol. 19
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74.
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome.
[electronic resource]
by
Corkey, B E
Hale, D E
Glennon, M C
Kelley, R I
Coates, P M
Kilpatrick, L
Stanley, C A
Producer:
19881026
In:
The Journal of clinical investigation
vol. 82
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75.
The L-3-hydroxyacyl-CoA dehydrogenase deficiency.
[electronic resource]
by
Hale, D E
Thorpe, C
Braat, K
Wright, J H
Roe, C R
Coates, P M
Hashimoto, T
Glasgow, A M
Producer:
19900517
In:
Progress in clinical and biological research
vol. 321
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76.
Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome.
[electronic resource]
by
Treem, W R
Witzleben, C A
Piccoli, D A
Stanley, C A
Hale, D E
Coates, P M
Watkins, J B
Producer:
19870127
In:
Hepatology (Baltimore, Md.)
vol. 6
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77.
Cholesteryl ester storage disease: pathologic changes in an affected fetus.
[electronic resource]
by
Desai, P K
Astrin, K H
Thung, S N
Gordon, R E
Short, M P
Coates, P M
Desnick, R J
Producer:
19870514
In:
American journal of medical genetics
vol. 26
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78.
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death.
[electronic resource]
by
Bennett, M J
Allison, F
Pollitt, R J
Manning, N J
Gray, R G
Green, A
Hale, D E
Coates, P M
Producer:
19870324
In:
Lancet (London, England)
vol. 1
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79.
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.
[electronic resource]
by
Bennett, M J
Coates, P M
Hale, D E
Millington, D S
Pollitt, R J
Rinaldo, P
Roe, C R
Tanaka, K
Producer:
19910110
In:
Journal of inherited metabolic disease
vol. 13
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80.
Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite family.
[electronic resource]
by
Haworth, J C
Demaugre, F
Booth, F A
Dilling, L A
Moroz, S P
Seshia, S S
Seargeant, L E
Coates, P M
Producer:
19921113
In:
The Journal of pediatrics
vol. 121
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