Arama Sonuçları - Bennett, Michael J.

Current Developments in Perinatology: The Fetus, Placenta and Newborn Yazar: Bennett, Michael J

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Mini-Review: Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency Yazar: Jethva, Reena, Bennett, Michael J., Vockley, Jerry

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Flunarizine Rescues Reduced Lifespan in CLN3 Triple Knock-Out Caenorhabditis elegans Model of Batten Disease Yazar: Kwon, Young-Joon, Falk, Marni J., Bennett, Michael J.

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Hiperinsulinismo na infância: quando apenas uma dosagem de insulina não é suficiente Yazar: Palladino, Andrew A., Bennett, Michael J., Stanley, Charles A.

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Flow injection tandem mass spectrometric measurement of ceramides of multiple chain lengths in biological samples Yazar: Chen, Jie, Narayan, Srinivas B., Edinger, Aimee L., Bennett, Michael J.

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Birefringence and DNA Condensation of Liquid Crystalline Chromosomes Yazar: Chow, Man H., Yan, Kosmo T. H., Bennett, Michael J., Wong, Joseph T. Y.

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Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short-chain fatty acid oxidation defects Yazar: Palladino, Andrew A., Chen, Jie, Kallish, Staci, Stanley, Charles A., Bennett, Michael J.

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Normal Biomarkers in an Acute Presentation in a Known Case of Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency Yazar: Alharbi, Hana, Bennett, Michael J, He, Miao, Master, Stephen R, Ganetzky, Rebecca D

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Screening for calcium channel modulators in CLN3 siRNA knock down SH-SY5Y neuroblastoma cells reveals a significant decrease of intracellular calcium levels by selected L-type calc... Yazar: an Haack, Kristina, Narayan, Srinivas B., Li, Haying, Warnock, Ashley, Tan, Lu, Bennett, Michael J.

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Strategies for Correcting Very Long Chain Acyl-CoA Dehydrogenase Deficiency Yazar: Tenopoulou, Margarita, Chen, Jie, Bastin, Jean, Bennett, Michael J., Ischiropoulos, Harry, Doulias, Paschalis-Thomas

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Choline Supplementation Alters Some Amino Acid Concentrations with No Change in Homocysteine in Children with Cystic Fibrosis and Pancreatic Insufficiency Yazar: Alshaikh, Belal, Schall, Joan I., Maqbool, Asim, Mascarenhas, Maria, Bennett, Michael J., Stallings, Virginia A.

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Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemia Yazar: Cocanougher, Benjamin, Aypar, Umut, McDonald, Amber, Hasadsri, Linda, Bennett, Michael J., Edward Highsmith, W., D׳Aco, Kristin

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ECHS1 Deficiency as a Cause of Severe Neonatal Lactic Acidosis Yazar: Ganetzky, Rebecca D., Bloom, Kaitlyn, Ahrens-Nicklas, Rebecca, Edmondson, Andrew, Deardorff, Matthew A., Bennett, Michael J., Ficicioglu, Can

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Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease Yazar: Cocanougher, Benjamin, Aypar, Umut, McDonald, Amber, Hasadsri, Linda, Bennett, Michael J., Edward Highsmith, W., D'Aco, Kristin

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Genetic Mapping of Glutaric Aciduria, Type 3, to Chromosome 7 and Identification of Mutations in C7orf10 Yazar: Sherman, Eric A., Strauss, Kevin A., Tortorelli, Silvia, Bennett, Michael J., Knerr, Ina, Morton, D. Holmes, Puffenberger, Erik G.

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Green Tea Polyphenols Control Dysregulated Glutamate Dehydrogenase in Transgenic Mice by Hijacking the ADP Activation Site Yazar: Li, Changhong, Li, Ming, Chen, Pan, Narayan, Srinivas, Matschinsky, Franz M., Bennett, Michael J., Stanley, Charles A., Smith, Thomas J.

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Power doppler ultrasound assessment of the relationship between age and ovarian perifollicular blood flow in women undergoing in vitro fertilization treatment Yazar: Costello, Michael F., Shrestha, Sanu M., Sjoblom, Peter, McNally, Glen, Bennett, Michael J., Steigrad, Stephen J., Hughes, Graeme J.

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Multi-organ Abnormalities and mTORC1 Activation in Zebrafish Model of Multiple Acyl-CoA Dehydrogenase Deficiency Yazar: Kim, Seok-Hyung, Scott, Sarah A., Bennett, Michael J., Carson, Robert P., Fessel, Joshua, Brown, H. Alex, Ess, Kevin C.

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Osmotic Blood-Brain Barrier Modification: Clinical Documentation by Enhanced CT Scanning and/or Radionuclide Brain Scanning Yazar: Neuwelt, Edward A., Specht, H. David, Howieson, John, Haines, James E., Bennett, Michael J., Hill, Suelien A., Frenkel, Eugene P.

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Genotype–phenotype correlations in CPT1A deficiency detected by newborn screening in Pacific populations Yazar: Bernhardt, Isaac, Glamuzina, Emma, Dowsett, Leah K., Webster, Dianne, Knoll, Detlef, Carpenter, Kevin, Bennett, Michael J., Maeda, Michelle, Wilson, Callum

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