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G Gascon

Showing results (41-50 of 75) with videos related to

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Journal of Child Neurology|April 1, 1992
Coincident neuraminidase and aspartoacylase deficiency associated with chromosome 9Q paracentric inversion in a Saudi familyG G Gascon, N G Youssef, S B Subramanyam, et al.
Journal of Child Neurology|March 1, 1995
Ataxia-oculomotor apraxia syndromeG G Gascon, N Abdo, D Sigut, 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 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.
Brain & Development|September 1, 1993
Combined oral isoprinosine-intraventricular alpha-interferon therapy for subacute sclerosing panencephalitisG Gascon, S Yamani, J Crowell, 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.
Epilepsy & Behavior : E&B|March 10, 2007
Landau-Kleffner syndrome with lateral temporal focal cortical dysplasia and mesial temporal sclerosis: a 30-year follow-upA Blum, G Tremont, J Donahue, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Prevalence of different types of lysosomal storage diseases in Saudi ArabiaP T Ozand, G Gascon, A al Aqeel, et al.
Neuropediatrics|December 1, 1995
Familial childhood primary lateral sclerosis with associated gaze paresisG G Gascon, P Chavis, A Yaghmour, et al.
Brain & Development|May 1, 1993
Chorea as a presentation of herpes simplex encephalitis relapseG G Gascon, A A al-Jarallah, E Okamoto, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Journal of Child Neurology|April 1, 1992
Coincident neuraminidase and aspartoacylase deficiency associated with chromosome 9Q paracentric inversion in a Saudi familyG G Gascon, N G Youssef, S B Subramanyam, et al.
Journal of Child Neurology|March 1, 1995
Ataxia-oculomotor apraxia syndromeG G Gascon, N Abdo, D Sigut, 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 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.
Brain & Development|September 1, 1993
Combined oral isoprinosine-intraventricular alpha-interferon therapy for subacute sclerosing panencephalitisG Gascon, S Yamani, J Crowell, 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.
Epilepsy & Behavior : E&B|March 10, 2007
Landau-Kleffner syndrome with lateral temporal focal cortical dysplasia and mesial temporal sclerosis: a 30-year follow-upA Blum, G Tremont, J Donahue, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Prevalence of different types of lysosomal storage diseases in Saudi ArabiaP T Ozand, G Gascon, A al Aqeel, et al.
Neuropediatrics|December 1, 1995
Familial childhood primary lateral sclerosis with associated gaze paresisG G Gascon, P Chavis, A Yaghmour, et al.
Brain & Development|May 1, 1993
Chorea as a presentation of herpes simplex encephalitis relapseG G Gascon, A A al-Jarallah, E Okamoto, et al.
Pageof 8