Search Results - "GREENE, C. L"

Energy and fat intake in obese and lean children at varying risk of obesity by MCGLOIN, A. F, LIVINGSTONE, M. B. E, GREENE, L. C, WEBB, S. E, GIBSON, J. M. A, JEBB, S. A, COLE, T. J, COWARD, W. A, WRIGHT, A, PRENTICE, A. M

“…This study compared lean children at high risk (HR) and low risk (LR) of obesity and obese children (OB) to assess the relationship between their energy (EI)…”
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Hiccups and gastroesophageal reflux disease as seen on high resolution esophageal manometry by Greene, C. L., Oh, D. S., Worrell, S. G., Hagen, J. A.

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Markedly elevated serum biotinidase activity may indicate glycogen storage disease type Ia by Wolf, B., Freehauf, C. L., Thomas, J. A., Gordon, P. L., Greene, C. L., Ward, J. C.

“…We report two children who presented with symptoms suggestive of biotinidase deficiency. Rather than deficiency, markedly elevated serum biotinidase activities…”
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GABA Receptor Antagonists Modulate Postmitotic Cell Migration in Slice Cultures of Embryonic Rat Cortex by Behar, Toby N., Schaffner, Anne E., Scott, Catherine A., Greene, Carolyn L., Barker, Jeffery L.

“…Recent studies indicate that GABA acts as a chemoattractant during rat cortical histogenesis. In vivo, GABA localizes in appropriate locations for a…”
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Glutamate Acting at NMDA Receptors Stimulates Embryonic Cortical Neuronal Migration by Behar, Toby N, Scott, Catherine A, Greene, Carolyn L, Wen, Xiling, Smith, Susan V, Maric, Dragan, Liu, Qi-Ying, Colton, Carol A, Barker, Jeffery L

“…During cortical development, embryonic neurons migrate from germinal zones near the ventricle into the cortical plate, where they organize into layers…”
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Mutation in the 4a-carbinolamine dehydratase gene leads to mild hyperphenylalaninemia with defective cofactor metabolism by CITRON, B. A, KAUFMAN, S, MILSTIEN, S, NAYLOR, E. W, GREENE, C. L, DAVIS, M. D

“…Hyperphenylalaninemias represent a major class of inherited metabolic disorders. They are most often caused by mutations in the phenylalanine hydroxylase gene…”
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Catastrophic metabolic encephalopathies in the newborn period. Evaluation and management by Greene, C L, Goodman, S I

“…The newborn who presents with neurologic symptoms such as seizures or lethargy due to inborn error of metabolism is an important problem. Although each inborn…”
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Inborn errors of metabolism and Reye syndrome: differential diagnosis by Greene, C L, Blitzer, M G, Shapira, E

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Dietary fibre, exercise and serum lipids and lipoprotein cholesterols in 12 to 15 year olds by Morley, R, Baker, BA, Greene, LC, Livingstone, MBE, Harland, PSEG, Lucas, A

“…Serum lipid and lipoprotein cholesterol levels track from childhood and are associated with risk of coronary heart disease. There is some evidence that these…”
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Molybdenum cofactor deficiency by Arnold, G L, Greene, C L, Stout, J P, Goodman, S I

“…We describe a new case of molybdenum cofactor deficiency, an underrecognized inborn error of metabolism that results in neonatal seizures and neurologic…”
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Relationship between early diet and subsequent cognitive performance during adolescence by Greene, L C, Lucas, A, Livingstone, M B, Harland, P S, Baker, B A

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Biological evaluation of pesticides released from temperature-responsive microcapsules by Greene, Larry C, Meyers, Paul A, Springer, Jeff T, Banks, Philip A

“…The pesticides diazinon, trifluralin, and alachlor were successfully encapsulated into temperature-responsive Intelimer microcapsules. The pesticides were…”
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Radiocephalometric evaluation of a family with mandibulofacial dysostosis by Bhatia, Sujata, Block, Michael S., Hoffman, David R., Lancaster, Diana, Greene, Carol L.

“…Persons from four generations of a family with mandibulofacial dysostosis (MFD), known as Treacher Collins (TC) Syndrome, were examined for the presence of…”
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Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency by Davidson-Mundt, A, Luder, A S, Greene, C L

“…Six infants and children with medium-chain acyl-coenzyme A dehydrogenase deficiency were found to have hyperuricemia during an acute episode. Hyperuricemia may…”
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Transient nonketotic hyperglycinemia in neonates by Luder, A S, Davidson, A, Goodman, S I, Greene, C L

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3‐hydroxy‐3‐methylglutaryl‐coenzyme a lyase deficiency: Report of five new patients by Gibson, K. M., Breuer, J., Kaiser, K., Nyhan, W. L., McCoy, E. E., Ferreira, P., Greene, C. L., Blitzer, M. G., Shapira, E., Reverte, F., Conde, C., Bagnell, P., Cole, D. E. C.

“…Summary Five new patients are reported and the pathogenesis of the hypoglycaemia without ketogenesis is discussed. This report extends a recent review.J…”
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Maternal phenylketonuria and hyperphenylalaninemia: implications for medical practice in the United States by Luder, A S, Greene, C L

“…The risk of maternal phenylketonuria and hyperphenylalaninemia syndrome, a preventable cause of severe birth defects and retardation with a near 100%…”
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Evaluation of a two-hour method for screening pathogens from stool specimens by GREENE, L. C, APPELBAUM, P. C, KELLOGG, J. A

“…Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Effects of dried distiller's grains with solubles and poultry fat as supplements for bermudagrass hay-based diet on blood metabolites, growth, meat and carcass characteristic of Spanish goats by Dangal, P, Kouakou, B, Greene, C L, Lee, J H, Sheed, J N

“…An abstract of a study by Kouakou et al evaluating the effects of replacing corn with Dried distiller's grains with solubles (DDGS), poultry fat, or DDGS plus…”
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683 Effects of dried distiller's grains with solubles and poultry fat as supplements for bermudagrass hay–based diet on blood metabolites, growth, meat and carcass characteristic of Spanish goats by Dangal, P., Kouakou, B., Greene, C. L., Lee, J. H., Sheed, J. N.

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