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Mitochondrial trifunctional protein / Proteins / Thiolase / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / NADH dehydrogenase / Newborn screening / HADHB / D-bifunctional protein deficiency / Biology / Health / Genetics


Articles in Press, Published on November 19, 2003 as[removed]PDR[removed][removed][removed]PEDIATRIC RESEARCH Copyright © 2003 International Pediatric Research Foundation, Inc. Vol. 55, No. 2, 2003
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Document Date: 2012-05-31 13:41:14

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City

Duesseldorf / SPIEKERKOETTER ET / New York / Kingston / Nashville / /

Company

acyl-CoA / enoyl-CoA / Sims HF / mCi / John Wiley and Sons / FAO / International Pediatric Research Foundation Inc. / Rohr / Brown / Lehman / LCHAD / Cox / VLCAD / LKAT / John Wiley & Sons / GIBCO Invitrogen Corporation / /

Country

Germany / United States / /

Currency

pence / /

/

Event

Product Issues / /

Facility

Vanderbilt Children’s Hospital / TFP complex / University of Texas Southwestern Medical Center / Vanderbilt University Medical Center / Heinrich Heine University Hospital / /

IndustryTerm

mutation site / splice site / detergent solution / treatment protocols / /

MedicalCondition

Mild TFP deficiency / acute fatty liver / retinitis pigmentosa / myopathy / seizures / correct disease / hereditary metabolic chorioretinopathy / biochemical deficiency / disorder / illness / liver disease / hypoketotic hypoglycemia / severe muscular hypotonia / hypoventilation / cardiomyopathy / respiratory failure / Shortness of breath / TFP deficiency / severe dilated cardiomyopathy / lethargy / mitochondrial trifunctional protein deficiency / dehydrogenase deficiency / patients’ TFP deficiency / Protein (TFP) Deficiency / infection / deficiency / individual peripheral neuropathy / disorders / Maternal liver diseases / LCHAD deficiency / rare genetic disorder / HELLP / later-onset myopathy / trifunctional protein deficiency / pericardial effusion / peripheral neuropathy / human trifunctional protein deficiency / fatal disease / pericardial and pleural effusions / lethal / early-onset disease / isolated thiolase deficiency / Maternal HELLP syndrome / myoglobinuria / MS / lethal and mild TFP deficiency / enzyme deficiency / lethal trifunctional protein deficiency / CoA dehydrogenase deficiency / disease / molecularly heterogeneous disorder / TFP DEFICIENCY AND MECHANISM OF DISEASE / Reye syndrome / HELLP syndrome / severe hypertrophic cardiomyopathy / lactic acidosis / progressive peripheral neuropathy / fetal fatty-acid oxidation disorder / Maternal liver disease / severe cardiomyopathy / Retinitis / mitochondrial trifunctional protein deficiencies / syndrome / milder TFP deficiency / fetal trifunctional protein deficiency / /

MedicalTreatment

antibiotics / treatment protocols / /

Organization

University of Texas Southwestern Medical Center / Dallas / International Pediatric Research Foundation / Vanderbilt University Medical Center / Department of General Pediatrics / National Institute of Health / Department of Pediatrics / Vanderbilt University School of Medicine / Heinrich Heine University Hospital / Pediatrics and Vanderbilt Children’s Hospital / ARNOLD W. STRAUSS Department of Pediatrics / /

Person

UTE SPIEKERKOETTER / Ann Neurol / Mitochondrial Trifunctional / ARNOLD W. STRAUSS / Washington Univer / Mitochondrial Trifunctional Protein / MICHAEL J. BENNETT / /

Position

General / head of bacteriophage T4 / /

Product

DS / Travert / subunit donor splice site mutations / patients / patient / one LCHAD-deficient patient / one healthy individual / /

ProvinceOrState

Alabama / New York / Texas / Tennessee / /

PublishedMedium

Molecular Biology / /

RadioStation

Ausubel FM / /

Technology

treatment protocols / genotype / Genomics / antibodies / /

URL

www.mrw2.interscience.wiley.com / www.scioncorp.com / www.invitrogen.com / /

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