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Pediatric Neurology|December 11, 1999
Hyperpipecolic acidemia: clinical, biochemical, and radiologic observationsM A Al-Essa, E Chaves-Carballo, P T Ozand
Brain & Development|November 1, 1994
The clinical spectrum of biotin-treatable encephalopathies in Saudi ArabiaO Dabbagh, J Brismar, G G Gascon, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|April 2, 2002
Tyrosinaemia type II: an easily diagnosed metabolic disorder with a rewarding therapeutic responseM A al-Essa, M S Rashed, P T Ozand
The Biochemical Journal|April 15, 1977
Effects of starvation and development on mitochondrial acetoacetyl-coenzyme A thiolase of rat liverW D Reed, P T Ozand, J T Tildon, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|April 2, 2002
Biotinidase deficiency: a treatable genetic disorder in the Saudi populationS Joshi, M A al-Essa, A Archibald, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 26, 1999
Clinical and brain 18fluoro-2-deoxyglucose positron emission tomographic findings in ethylmalonic aciduria, a progressive neurometabolic diseaseM A al-Essa, L A al-Shamsan, P T Ozand
Brain & Development|November 1, 1994
Malonic aciduriaP T Ozand, W L Nyhan, A al Aqeel, et al.
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