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Metabolism / Fatty acids / Developmental biology / Fatty-acid metabolism disorder / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Mitochondrial trifunctional protein deficiency / Mitochondrial trifunctional protein / Rare diseases / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Biology / Health / Medicine


Am J Physiol Endocrinol Metab 284: E1098–E1105, 2003. First published February 11, 2003; [removed]ajpendo[removed]Human placenta metabolizes fatty acids: implications for fetal fatty acid oxidation disorders and mat
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Document Date: 2012-05-31 13:41:14

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San Leandro / Dallas / Burlingame / Carpinteria / Boston / Bradford / New York / Nashville / Oostheim / St. Louis / /

Company

Zymed Laboratories / acyl-CoA / Brix AE / Burlina AB / Sims HF / FAO / SPSS / Arnold W. Strauss4 / /

Country

Netherlands / United States / /

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pence / USD / /

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Event

Product Issues / /

Facility

Vanderbilt University / Vanderbilt Children’s Hospital / University of Texas-Southwestern Medical Center / University School / Medical College of Georgia / /

IndustryTerm

active site / image analysis software / media containing glucose / large energy requirement / 13C-labeled stable isotope technology / high energy requirements / long chain / energy / energy production / carrier frequency / energy source / important metabolic energy source / neutral buffered formalin solution / energy requirements / energy substrate source / statistical software / food intake / important site / energy-producing pathway / placental and fetal energy needs / /

MedicalCondition

Tein I. Metabolic disease / acute fatty liver / maternal liver diseases / low platelets syndrome / LCHAD deficiency / HELLP / Trifunctional protein deficiency / JE / placental insufficiency / fatty acid oxidation disorders / complete trifunctional protein deficiency / SCAD deficiency / coma / maternal diseases / freeradical-induced lipid membrane peroxidative injury / fetal fatty acid oxidation disorders / Human trifunctional protein deficiency / MCAD deficiency / CoA deficiency / primary carnitine deficiency / significant maternal hepatic dysfunction / disorder / liver disease / hypoketotic hypoglycemia / recently identified disorder / VLCAD deficiency / prenatal fetal death / free radical-induced lipid peroxidation injury / CoA dehydrogenase deficiency / liver diseases / Reye syndrome / Wilcken B. Recurrent acute fatty liver / diabetes / hepatic encephalopathy / HELLP syndrome / maternal illness / neonatal hypoglycemia / fetal fatty-acid oxidation disorder / dehydrogenase deficiency / maternal liver disease / Pihko H. Pregnancy complications / deficiency / preeclampsia / maternal acute fatty liver / preeclampsia / acute fatty liver / fatal disorders / /

Organization

Vanderbilt Children’s Hospital / Human Studies Committee / Washington University School of Medicine / Medical College of Georgia / Vanderbilt University / American Physiological Society / University of Texas / /

Person

Van Werkhoven / Charles D. Lipoprotein / Prem Shekhawat / Beverly Rogers / D. Michael Nelson / Dinesh Rakheja / James K. Dias / Van Pampus / Lindsey JR / Michael J. Bennett / Karen Hutton / /

Position

Weglicki WB / Coates PM / representative / /

Product

fungizone / penicillin / chorionic gonadotropin / Triton / late-gestation / mice / fetuses / /

ProvinceOrState

Texas / Missouri / Tennessee / Georgia / /

RadioStation

Innes AM / Campbell FM / Wittmaack FM / /

Technology

Alpha / microwave / 13C-labeled stable isotope technology / /

URL

http /

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