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Bassam R Ali

Showing results (41-50 of 173) with videos related to

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Investigative Ophthalmology & Visual Science|April 19, 2014
Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathyReham M Milhem, Salma Ben-Salem, Lihadh Al-Gazali, et al.
The Pharmacogenomics Journal|November 12, 2025
Comparative analysis of point-of-care bedside cyp2c19-testing guided anti-platelet therapy versus conventional therapies for cardiovascular diseases: a systematic review and meta-analysisMohammed Khattab, Mohamed Baguneid, George P Patrinos, et al.
Saudi Medical Journal|November 26, 2009
A novel mutation in ARG1 gene is responsible for arginase deficiency in an Asian familyJozef L Hertecant, Lihadh I Al-Gazali, Noushad S Karuvantevida, et al.
Frontiers in Cell and Developmental Biology|February 7, 2022
Role of Ceramides in the Molecular Pathogenesis and Potential Therapeutic Strategies of Cardiometabolic Diseases: What we Know so FarYoussef M Shalaby, Anas Al Aidaros, Anjana Valappil, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 14, 2014
The mutational spectrum of the NF1 gene in neurofibromatosis type I patients from UAESalma Ben-Salem, Aisha M Al-Shamsi, Bassam R Ali, et al.
Sensors (Basel, Switzerland)|September 10, 2021
Electrical Detection of Innate Immune CellsMahmoud Al Ahmad, Rasha A Nasser, Lillian J A Olule, et al.
Journal of Molecular Neuroscience : MN|November 14, 2019
Evaluating the Role of MAST1 as an Intellectual Disability Disease Gene: Identification of a Novel De Novo Variant in a Patient with Developmental DisabilitiesAfif Ben-Mahmoud, Aisha M Al-Shamsi, Bassam R Ali, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 27, 2018
West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutationsQudsia Shaukat, Jozef Hertecant, Ayman W El-Hattab, et al.
Frontiers in Genetics|November 11, 2020
Proteostasis Regulation in the Endoplasmic Reticulum: An Emerging Theme in the Molecular Pathology and Therapeutic Management of Familial HypercholesterolemiaDeepu Oommen, Praseetha Kizhakkedath, Aseel A Jawabri, et al.
Human Genetics|October 2, 2021
Clinical implementation of drug metabolizing gene-based therapeutic interventions worldwideEvangelia Eirini Tsermpini, Zeina N Al-Mahayri, Bassam R Ali, et al.
Pageof 18

Showing results (41-50 of 173) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|April 19, 2014
Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathyReham M Milhem, Salma Ben-Salem, Lihadh Al-Gazali, et al.
The Pharmacogenomics Journal|November 12, 2025
Comparative analysis of point-of-care bedside cyp2c19-testing guided anti-platelet therapy versus conventional therapies for cardiovascular diseases: a systematic review and meta-analysisMohammed Khattab, Mohamed Baguneid, George P Patrinos, et al.
Saudi Medical Journal|November 26, 2009
A novel mutation in ARG1 gene is responsible for arginase deficiency in an Asian familyJozef L Hertecant, Lihadh I Al-Gazali, Noushad S Karuvantevida, et al.
Frontiers in Cell and Developmental Biology|February 7, 2022
Role of Ceramides in the Molecular Pathogenesis and Potential Therapeutic Strategies of Cardiometabolic Diseases: What we Know so FarYoussef M Shalaby, Anas Al Aidaros, Anjana Valappil, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 14, 2014
The mutational spectrum of the NF1 gene in neurofibromatosis type I patients from UAESalma Ben-Salem, Aisha M Al-Shamsi, Bassam R Ali, et al.
Sensors (Basel, Switzerland)|September 10, 2021
Electrical Detection of Innate Immune CellsMahmoud Al Ahmad, Rasha A Nasser, Lillian J A Olule, et al.
Journal of Molecular Neuroscience : MN|November 14, 2019
Evaluating the Role of MAST1 as an Intellectual Disability Disease Gene: Identification of a Novel De Novo Variant in a Patient with Developmental DisabilitiesAfif Ben-Mahmoud, Aisha M Al-Shamsi, Bassam R Ali, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 27, 2018
West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutationsQudsia Shaukat, Jozef Hertecant, Ayman W El-Hattab, et al.
Frontiers in Genetics|November 11, 2020
Proteostasis Regulation in the Endoplasmic Reticulum: An Emerging Theme in the Molecular Pathology and Therapeutic Management of Familial HypercholesterolemiaDeepu Oommen, Praseetha Kizhakkedath, Aseel A Jawabri, et al.
Human Genetics|October 2, 2021
Clinical implementation of drug metabolizing gene-based therapeutic interventions worldwideEvangelia Eirini Tsermpini, Zeina N Al-Mahayri, Bassam R Ali, et al.
Pageof 18