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Results of search for 'au:"Barshop, B A"', page 1 of 2
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Authors
Abdenur, J E
Alberts, A S
Barshop, B A
Frieden, C
Gruber, H E
Haas, R H
Holm, J
Jones, K L
Leslie, J
Markusic, D
Marsden, D
McGowan, K A
Naviaux, R K
Nyhan, W L
Prodanos, C
Rice, M
Shelton, G D
Sweetman, L
Willis, M
Wolff, J
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Amino Acid Metabolism, Inborn Errors
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Child, Preschool
DNA, Mitochondrial
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Infant, Newborn
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analysis
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deficiency
enzymology
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Your search returned 29 results.
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1.
Analysis of the interaction of rabbit skeletal muscle adenylate deaminase with myosin subfragments. A kinetically regulated system.
[electronic resource]
by
Barshop, B A
Frieden, C
Producer:
19840511
In:
The Journal of biological chemistry
vol. 259
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No items available.
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2.
Diet change in the management of metabolic encephalomyopathies.
[electronic resource]
by
Haas, R H
Barshop, B A
Producer:
19980624
In:
BioFactors (Oxford, England)
vol. 7
Online resources:
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3.
Creatine kinase and uric acid: early warning for metabolic imbalance resulting from disorders of fatty acid oxidation.
[electronic resource]
by
Marsden, D
Nyhan, W L
Barshop, B A
Producer:
20020205
In:
European journal of pediatrics
vol. 160
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4.
Severe hypertriglyceridemia and recurrent pancreatitis in a girl with type Ia glycogen storage disease and type III hyperlipoproteinemia.
[electronic resource]
by
Vivatrat, N
Barshop, B A
Jones, K L
Producer:
20100106
In:
American journal of medical genetics. Part A
vol. 149A
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5.
Analysis of numerical methods for computer simulation of kinetic processes: development of KINSIM--a flexible, portable system.
[electronic resource]
by
Barshop, B A
Wrenn, R F
Frieden, C
Producer:
19830811
In:
Analytical biochemistry
vol. 130
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6.
Kinetic studies of mutant human adenylosuccinase.
[electronic resource]
by
Barshop, B A
Alberts, A S
Gruber, H E
Producer:
19891219
In:
Biochimica et biophysica acta
vol. 999
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7.
Pitfalls in the detection of heterozygosity by allopurinol in a variant form of ornithine carbamoyltransferase deficiency.
[electronic resource]
by
Barshop, B A
Nyhan, W L
Climent, C
Rubio, V
Producer:
20020221
In:
Journal of inherited metabolic disease
vol. 24
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8.
Oxidative metabolism in Rett syndrome: 1. Clinical studies.
[electronic resource]
by
Haas, R H
Light, M
Rice, M
Barshop, B A
Producer:
19951030
In:
Neuropediatrics
vol. 26
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9.
Positive newborn screen in the biochemically normal infant of a mother with treated holocarboxylase synthetase deficiency.
[electronic resource]
by
Nyhan, W L
Willis, M
Barshop, B A
Gangoiti, J
Producer:
20130805
In:
Journal of inherited metabolic disease
vol. 32 Suppl 1
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10.
Treatment of the acute crisis in maple syrup urine disease.
[electronic resource]
by
Nyhan, W L
Rice-Kelts, M
Klein, J
Barshop, B A
Producer:
19980707
In:
Archives of pediatrics & adolescent medicine
vol. 152
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11.
Unusual presentation of propionic acidaemia as isolated cardiomyopathy.
[electronic resource]
by
Lee, T M
Addonizio, L J
Barshop, B A
Chung, W K
Producer:
20130805
In:
Journal of inherited metabolic disease
vol. 32 Suppl 1
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12.
Studies of mutant human adenylosuccinate lyase.
[electronic resource]
by
Barshop, B A
Alberts, A S
Laikind, P K
Gruber, H E
Producer:
19900320
In:
Advances in experimental medicine and biology
vol. 253A
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13.
Excretion of hippuric acid during sodium benzoate therapy in patients with hyperglycinaemia or hyperammonaemia.
[electronic resource]
by
Barshop, B A
Breuer, J
Holm, J
Leslie, J
Nyhan, W L
Producer:
19890822
In:
Journal of inherited metabolic disease
vol. 12
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14.
Successful Domino Liver Transplantation from a Patient with Methylmalonic Acidemia.
[electronic resource]
by
Khanna, A
Gish, R
Winter, S C
Nyhan, W L
Barshop, B A
Publication details:
JIMD reports
2016
In:
JIMD reports
vol. 25
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15.
Analysis of organic acids, amino acids, and carnitine in dogs with lipid storage myopathy.
[electronic resource]
by
Shelton, G D
Nyhan, W L
Kass, P H
Barshop, B A
Haas, R H
Producer:
19980904
In:
Muscle & nerve
vol. 21
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16.
Mitochondrial tubulopathy: the many faces of mitochondrial disorders.
[electronic resource]
by
Lee, Y S
Yap, H K
Barshop, B A
Lee, Y S
Rajalingam, S
Loke, K Y
Producer:
20011204
In:
Pediatric nephrology (Berlin, Germany)
vol. 16
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17.
Sensitive assay for mitochondrial DNA polymerase gamma.
[electronic resource]
by
Naviaux, R K
Markusic, D
Barshop, B A
Nyhan, W L
Haas, R H
Producer:
19991021
In:
Clinical chemistry
vol. 45
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18.
Kearns-Sayre syndrome presenting as 2-oxoadipic aciduria.
[electronic resource]
by
Barshop, B A
Nyhan, W L
Naviaux, R K
McGowan, K A
Friedlander, M
Haas, R H
Producer:
20000229
In:
Molecular genetics and metabolism
vol. 69
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19.
Luminescent immobilized enzyme test systems for inorganic pyrophosphate: assays using firefly luciferase and nicotinamide-mononucleotide adenylyl transferase or adenosine-5'-triphosphate sulfurylase.
[electronic resource]
by
Barshop, B A
Adamson, D T
Vellom, D C
Rosen, F
Epstein, B L
Seegmiller, J E
Producer:
19911206
In:
Analytical biochemistry
vol. 197
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20.
Malonic aciduria in Maltese dogs: normal methylmalonic acid concentrations and malonyl-CoA decarboxylase activity in fibroblasts.
[electronic resource]
by
O'Brien, D P
Barshop, B A
Faunt, K K
Johnson, G C
Gibson, K M
Shelton, G D
Producer:
20000124
In:
Journal of inherited metabolic disease
vol. 22
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