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Pediatric Neurology|December 11, 1999
Hyperpipecolic acidemia: clinical, biochemical, and radiologic observationsM A Al-Essa, E Chaves-Carballo, P T OzandBrain & 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 OzandPediatric Research|September 1, 1995
Diagnosis of inborn errors of metabolism from blood spots by acylcarnitines and amino acids profiling using automated electrospray tandem mass spectrometryM S Rashed, P T Ozand, M P Bucknall, et al.Human Genetics|May 1, 1990
Cytogenetic characterization of ataxia telangiectasia (AT) heterozygotes using lymphoblastoid cell lines and chronic gamma-irradiationM Waghray, S al-Sedairy, P T Ozand, et al.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 OzandJournal of Chromatography|July 1, 1992
Quantitative measurement of N-acetyl-L-aspartic acid in urine by gas chromatography with negative-ion chemical ionization mass spectrometryH J Leis, P T Ozand, A al Odaib, et al.Pageof 29