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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
Revista De Neurologia|May 8, 2000
[Genetic encephalopathies in a newborn]E Chaves-Carballo, M A al-Essa
Neurosciences (Riyadh, Saudi Arabia)|November 27, 2013
X-linked adrenoleukodystrophy. The Saudi experienceM A Al-Essa, N A Sakati, S M Bakheet, 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
Classic homocystinuria: clinical, biochemical and radiological observations, and therapeutic outcome of 24 Saudi patientsM A al-Essa, M S Rashed, P T Ozand
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
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
Pediatric Neurology|February 11, 2000
Clinical and cerebral FDG PET scan in a patient with Krabbe's diseaseM A Al-Essa, S M Bakheet, Z J Patay, et al.
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