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Moeen Al-Sayed

Showing results (1-10 of 13) with videos related to

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Fertility and Sterility|March 6, 2007
Preimplantation genetic diagnosis for Zellweger syndromeMoeen Al-Sayed, Saad Al-Hassan, Mohamed Rashed, et al.
BMC Research Notes|March 20, 2010
Novel mutations underlying argininosuccinic aciduria in Saudi ArabiaFaiqa Imtiaz, Moeen Al-Sayed, Danyah Trabzuni, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
GM2 gangliosidosis in Saudi Arabia: multiple mutations and considerations for future carrier screeningNamik Kaya, Mohammad Al-Owain, Nada Abudheim, et al.
Molecular Genetics and Metabolism Reports|July 20, 2018
The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patientsZuhair N Al-Hassnan, Ola A Khalifa, Dalal K Bubshait, et al.
Journal of Inherited Metabolic Disease|June 23, 2010
Medium-chain acyl-CoA dehydrogenase deficiency in Saudi Arabia: incidence, genotype, and preventive implicationsZuhair N Al-Hassnan, Faiqa Imtiaz, Mohamed Al-Amoudi, et al.
Molecular Genetics and Metabolism|July 19, 2011
Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern originFaiqa Imtiaz, Mohamed S Rashed, Bashayer Al-Mubarak, et al.
European Journal of Pediatrics|March 5, 2009
Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiencyMuhammad Faiyaz-Ul-Haque, Mohammed Al-Owain, Fouad Al-Dayel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIIINamik Kaya, Hesham Aldhalaan, Banan Al-Younes, et al.
Journal of Inherited Metabolic Disease|September 20, 2012
Clinical and biochemical features associated with BCS1L mutationMohammed Al-Owain, Dilek Colak, Albandary Albakheet, et al.
Ophthalmic Genetics|July 5, 2019
Optic neuropathy in classical methylmalonic acidemiaMohammed AlOwain, Ola Ali Khalifa, Zahra Al Sahlawi, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Fertility and Sterility|March 6, 2007
Preimplantation genetic diagnosis for Zellweger syndromeMoeen Al-Sayed, Saad Al-Hassan, Mohamed Rashed, et al.
BMC Research Notes|March 20, 2010
Novel mutations underlying argininosuccinic aciduria in Saudi ArabiaFaiqa Imtiaz, Moeen Al-Sayed, Danyah Trabzuni, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
GM2 gangliosidosis in Saudi Arabia: multiple mutations and considerations for future carrier screeningNamik Kaya, Mohammad Al-Owain, Nada Abudheim, et al.
Molecular Genetics and Metabolism Reports|July 20, 2018
The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patientsZuhair N Al-Hassnan, Ola A Khalifa, Dalal K Bubshait, et al.
Journal of Inherited Metabolic Disease|June 23, 2010
Medium-chain acyl-CoA dehydrogenase deficiency in Saudi Arabia: incidence, genotype, and preventive implicationsZuhair N Al-Hassnan, Faiqa Imtiaz, Mohamed Al-Amoudi, et al.
Molecular Genetics and Metabolism|July 19, 2011
Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern originFaiqa Imtiaz, Mohamed S Rashed, Bashayer Al-Mubarak, et al.
European Journal of Pediatrics|March 5, 2009
Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiencyMuhammad Faiyaz-Ul-Haque, Mohammed Al-Owain, Fouad Al-Dayel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIIINamik Kaya, Hesham Aldhalaan, Banan Al-Younes, et al.
Journal of Inherited Metabolic Disease|September 20, 2012
Clinical and biochemical features associated with BCS1L mutationMohammed Al-Owain, Dilek Colak, Albandary Albakheet, et al.
Ophthalmic Genetics|July 5, 2019
Optic neuropathy in classical methylmalonic acidemiaMohammed AlOwain, Ola Ali Khalifa, Zahra Al Sahlawi, et al.
Pageof 2