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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.
The Journal of Pediatrics|June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, S M Willi, P Rinaldo, et al.
American Journal of Medical Genetics. Supplement|January 1, 1988
Therapeutic modification of membrane lipid abnormalities in juvenile neuronal ceroid-lipofuscinosis (Batten disease)M J Bennett, G P Hosking, R Gayton, et al.
The Plant Journal : for Cell and Molecular Biology|March 22, 2001
Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1G Parry, A Delbarre, A Marchant, et al.
Annals of Emergency Medicine|August 25, 1999
Hypoketotic hypoglycemic coma in a 21-month-old childM A Hostetler, G L Arnold, R Mooney, et al.
JIMD Reports|February 23, 2013
Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA DeficiencyA A M Morris, S E Olpin, M J Bennett, et al.
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