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Biology of the Neonate|August 10, 2002
Angiotensin-converting enzyme gene insertion/deletion polymorphism in Kuwaiti children with retinopathy of prematurityM Z Haider, L V Devarajan, M Al-Essa, et al.Journal of Child Neurology|April 1, 1992
Biochemical heterogeneity of infantile central nervous system spongy degenerationS B Subramanyam, A Tipirneni, N Youssef, et al.Journal of Human Genetics|August 17, 2000
Structural and functional study of K453E mutant protective protein/cathepsin A causing the late infantile form of galactosialidosisK Takiguchi, K Itoh, M Shimmoto, et al.Advances in Experimental Medicine and Biology|January 1, 1980
The effects of ethanol on developing catecholamine neuronsN Detering, R Collins, R L Hawkins, et al.Journal of Child Neurology|April 1, 1992
Riyadh chromosome breakage syndrome: mental retardation with depigmentation of the skin and hairP T Ozand, M Waghray, J D Cook, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|April 16, 1998
Nebulisation of surfactants in an animal model of neonatal respiratory distressT F Fok, M al-Essa, M Dolovich, et al.Journal of Inherited Metabolic Disease|January 1, 1991
3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency in Saudi ArabiaP T Ozand, A al Aqeel, G Gascon, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1976
Growth of human diploid fibroblasts in the absence of glucose utilizationH R Zielke, P T Ozand, J T Tildon, et al.Journal of Cellular Physiology|April 1, 1978
Reciprocal regulation of glucose and glutamine utilization by cultured human diploid fibroblastsH R Zielke, P T Ozand, J T Tildon, et al.The American Journal of Physiology|May 1, 1976
Ability of exogenous alanine to lower blood beta-hydroxybutyrate during development in ratsP T Ozand, J T Tildon, J H Stevenson, et al.Pageof 29