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Journal of Child Neurology|April 1, 1992
Treatment of inherited neurometabolic diseases: the futureP T Ozand, G G GasconLife Sciences|April 11, 1983
Alterations of catecholamine enzymes in several brain regions of victims of sudden infant death syndromeP T Ozand, J T TildonBrain & Development|November 1, 1994
A new patient with alpha-ketoglutaric aciduria and progressive extrapyramidal tract diseaseA al Aqeel, M Rashed, P T Ozand, et al.Brain & Development|November 1, 1994
Unusual presentations of propionic acidemiaP T Ozand, M Rashed, G G Gascon, et al.Brain & Development|November 1, 1994
Comparative frequency and severity of hypoglycemia in selected organic acidemias, branched chain amino acidemia, and disorders of fructose metabolismH G Worthen, A al Ashwal, P T Ozand, et al.Annals of Saudi Medicine|July 1, 1994
Glutaric aciduria yype 1: First reported cases in three Saudi patientsR Coates, M Rashed, Z Rahbeeni, et al.Journal of Child Neurology|April 1, 1992
A patient with propionic acidemia managed with continuous insulin infusion and total parenteral nutritionA Kalloghlian, H Gleispach, P T OzandBrain & Development|July 21, 1999
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography of the brain, MR spectroscopy, and therapeutic attempts in methylenetetrahydrofolate reductase deficiencyM A Al-Essa, A Al Amir, M Rashed, et al.Ophthalmic Genetics|June 1, 1997
Peroxisomal bifunctional enzyme deficiency with associated retinal findingsS A Al-Hazzaa, P T OzandAmerican Journal of Medical Genetics|February 1, 1990
Aspartoacylase deficiency and Canavan disease in Saudi ArabiaP T Ozand, G G Gascon, M DhallaPageof 29