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Pediatric Research|February 1, 1979
Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's diseaseB M Atkin, N R Buist, M F Utter, et al.Magma (New York, N.Y.)|November 13, 2004
Cerebral blood flow response to a hypoxic-ischemic insult differs in neonatal and juvenile ratsM Qiao, P Latta, T Foniok, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1984
Ophthalmic manifestations of infantile phytanic acid storage diseaseR G Weleber, A C Tongue, N G Kennaway, et al.American Journal of Public Health|December 1, 1987
Computerized surveillance of errors in newborn screening practiceJ M Tuerck, N R Buist, M R Skeels, et al.Pediatrics|February 1, 1979
Neonatal hypothyroidism detected by the Northwest Regional Screening ProgramS H LaFranchi, W H Murphey, T P Foley, et al.Pediatrics|August 1, 1991
Verbal dyspraxia in treated galactosemiaC D Nelson, D D Waggoner, G N Donnell, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
A new amino acid mixture permits new approaches to the treatment of phenylketonuriaN R Buist, A P Prince, K L Huntington, et al.Neurology|October 1, 1994
A rippling muscle disease gene is localized to 1q41: evidence for multiple genesD A Stephan, N R Buist, A B Chittenden, et al.American Journal of Human Genetics|November 15, 2000
Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b geneJ A Keightley, R Anitori, M D Burton, et al.The Journal of Pediatrics|February 1, 1994
Effect of ascorbate or N-acetylcysteine treatment in a patient with hereditary glutathione synthetase deficiencyA Jain, N R Buist, N G Kennaway, et al.Pageof 14