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Pediatric Research
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November 25, 2003
General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover
Ute Spiekerkoetter, Zaza Khuchua, Zou Yue, et al.
Pediatric Research
|
March 7, 2003
Effect of L-carnitine supplementation on cardiac carnitine palmitoyltransferase activities and plasma carnitine concentrations in adriamycin-treated rats
Hye-Ran Yoon, Young Mi Hong, Richard L Boriack, et al.
Brain : a Journal of Neurology
|
July 9, 2004
CLN3L, a novel protein related to the Batten disease protein, is overexpressed in Cln3-/- mice and in Batten disease
Srinivas B Narayan, Johanne V Pastor, Hannah M Mitchison, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|
July 4, 2012
Mutations in long-chain 3-hydroxyacyl coenzyme a dehydrogenase are associated with placental maternal floor infarction/massive perivillous fibrin deposition
Adrienne Carruth Griffin, Arnold W Strauss, Michael J Bennett, et al.
Clinical Chemistry
|
December 1, 2021
Normal Biomarkers in an Acute Presentation in a Known Case of Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
Hana Alharbi, Michael J Bennett, Miao He, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
January 15, 2010
Women's expectations of management in their next pregnancy after an unexplained stillbirth: an Internet-based empirical study
Stephen J Robson, Leo R Leader, Keith B G Dear, et al.
Medical Hypotheses
|
August 9, 2005
Increased ratio of saturated to unsaturated C18 fatty acids in colonic adenocarcinoma: implications for cryotherapy and lipid raft function
Dinesh Rakheja, Payal Kapur, Mai P Hoang, et al.
Molecular Genetics and Metabolism
|
November 3, 2012
Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short-chain fatty acid oxidation defects
Andrew A Palladino, Jie Chen, Staci Kallish, et al.
American Journal of Obstetrics and Gynecology
|
September 19, 2002
Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations
Zi Yang, Yiwen Zhao, Michael J Bennett, et al.
Muscle & Nerve
|
December 25, 2003
Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein
Ute Spiekerkoetter, Michael J Bennett, Bruria Ben-Zeev, et al.
Page
of 16
Search research articles
Search
Showing results (61-70 of 156) with videos related to
Sort By:
Page
of 16
Pediatric Research
|
November 25, 2003
General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover
Ute Spiekerkoetter, Zaza Khuchua, Zou Yue, et al.
Pediatric Research
|
March 7, 2003
Effect of L-carnitine supplementation on cardiac carnitine palmitoyltransferase activities and plasma carnitine concentrations in adriamycin-treated rats
Hye-Ran Yoon, Young Mi Hong, Richard L Boriack, et al.
Brain : a Journal of Neurology
|
July 9, 2004
CLN3L, a novel protein related to the Batten disease protein, is overexpressed in Cln3-/- mice and in Batten disease
Srinivas B Narayan, Johanne V Pastor, Hannah M Mitchison, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|
July 4, 2012
Mutations in long-chain 3-hydroxyacyl coenzyme a dehydrogenase are associated with placental maternal floor infarction/massive perivillous fibrin deposition
Adrienne Carruth Griffin, Arnold W Strauss, Michael J Bennett, et al.
Clinical Chemistry
|
December 1, 2021
Normal Biomarkers in an Acute Presentation in a Known Case of Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
Hana Alharbi, Michael J Bennett, Miao He, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
January 15, 2010
Women's expectations of management in their next pregnancy after an unexplained stillbirth: an Internet-based empirical study
Stephen J Robson, Leo R Leader, Keith B G Dear, et al.
Medical Hypotheses
|
August 9, 2005
Increased ratio of saturated to unsaturated C18 fatty acids in colonic adenocarcinoma: implications for cryotherapy and lipid raft function
Dinesh Rakheja, Payal Kapur, Mai P Hoang, et al.
Molecular Genetics and Metabolism
|
November 3, 2012
Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short-chain fatty acid oxidation defects
Andrew A Palladino, Jie Chen, Staci Kallish, et al.
American Journal of Obstetrics and Gynecology
|
September 19, 2002
Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations
Zi Yang, Yiwen Zhao, Michael J Bennett, et al.
Muscle & Nerve
|
December 25, 2003
Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein
Ute Spiekerkoetter, Michael J Bennett, Bruria Ben-Zeev, et al.
Page
of 16