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Pediatric Emergency Care|December 23, 1999
Delayed diagnosis of fatal medium-chain acyl-CoA dehydrogenase deficiency in a childA K Shetty, R D Craver, J A Harris, et al.
The Journal of Pediatrics|September 1, 1996
Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapyM H Fries, P Rinaldo, E Schmidt-Sommerfeld, et al.
European Journal of Pediatrics|December 1, 1990
Medium-chain acyl CoA dehydrogenase deficiency: electron microscopic differentiation from Reye syndromeR Santer, E Schmidt-Sommerfeld, Y K Leung, et al.
Annals of Clinical Biochemistry|January 1, 1994
Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spotsM J Bennett, M C Ragni, R J Ostfeld, et al.
Neurosurgery Clinics of North America|October 22, 2003
Intrathecal medication deliveryRichard D Penn
Pediatric Research|August 1, 1977
Carnitine content of blood and amniotic fluidP Hahn, J P Skala, D W Seccombe, et al.
Neurosurgery Clinics of North America|July 1, 1990
Medical and surgical treatment of spasticityR D Penn
Neurologic Clinics|May 1, 1985
Drug pumps for treatment of neurologic diseases and painR D Penn
Neurosurgery|March 1, 1980
Cerebral edema and neurological function in human beingsR D Penn
Neurosurgery|January 1, 1982
Chronic cerebellar stimulation for cerebral palsy: a reviewR D Penn
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