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Molecular Genetics and Metabolism|March 13, 2001
Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencyD Matern, B M Schehata, P Shekhawa, et al.
European Journal of Clinical Investigation|March 1, 1992
Determinants of fasting plasma triglyceride levels: metabolism of hepatic and intestinal lipoproteinsJ A Cortner, N A Le, P M Coates, et al.
American Journal of Medical Genetics|October 1, 1991
Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, PennsylvaniaD H Morton, M J Bennett, L E Seargeant, et al.
Bioscience Reports|February 1, 1995
Cholesterol enhances cationic liposome-mediated DNA transfection of human respiratory epithelial cellsM J Bennett, M H Nantz, R P Balasubramaniam, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 1, 1986
Chorionic villus sampling. Clinical experience in 50 diagnostic casesD M Wass, P S Warren, L A Stewart, et al.
Pediatric Research|February 1, 1985
Urinary sediment dolichol excretion in patients with Batten disease and other neurodegenerative and storage disordersM J Bennett, N J Mathers, F W Hemming, et al.
Human Molecular Genetics|April 6, 2000
Batten disease: evaluation of CLN3 mutations on protein localization and functionR E Haskell, C J Carr, D A Pearce, et al.
Mental Retardation|October 1, 1994
Detection of metabolic disorders among selectively screened people with idiopathic mental retardationM B Kurtz, B Finucane, K Hyland, et al.
The Journal of Pediatrics|May 1, 1993
Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic methodE Schmidt-Sommerfeld, D Penn, M Duran, et al.
Neurology|February 5, 1999
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathyI Tein, R H Haslam, W J Rhead, et al.
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