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R Ali

Showing results (631-640 of 1,192) with videos related to

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Biorxiv : the Preprint Server for Biology|December 15, 2025
DNA extraction and virome processing methods strongly influence recovered human gut viral community characteristicsLuke S Hillary, Trina A Knotts, Sean H Adams, et al.
Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|March 4, 2026
Pregnancy after bariatric surgery: persistent obesity and longer time to conception influences peripartum outcomes more than the type of operationMiaoli E Bloemhard, Ariana A Schmulbach, Kanksha Koti, et al.
Frontiers in Physiology|January 25, 2021
<i>Ex vivo</i> Methods for Measuring Cardiac Muscle Mechanical PropertiesWalter E Knight, Hadi R Ali, Stephanie J Nakano, et al.
Neuroradiology|September 20, 2006
Tumor lysis syndrome as a contributory factor to the development of reversible posterior leukoencephalopathyA Ozkan, B Hakyemez, F Ozkalemkas, et al.
Annals of Surgery|October 31, 2013
Single-site robotic cholecystectomy in a broadly inclusive patient population: a prospective studyTamas J Vidovszky, Aaron D Carr, Gina N Farinholt, et al.
AIDS (London, England)|July 1, 1991
HIV prevalence and risk behaviours for HIV transmission in South Australian prisonsM D Gaughwin, R M Douglas, C Liew, et al.
Clinical Endocrinology|August 21, 2023
The I-CAH Registry: A platform for international collaboration for improving knowledge and clinical care in congenital adrenal hyperplasiaXanthippi Tseretopoulou, Jillian Bryce, Minglu Chen, et al.
Human Molecular Genetics|September 23, 2010
Cone and rod photoreceptor transplantation in models of the childhood retinopathy Leber congenital amaurosis using flow-sorted Crx-positive donor cellsJ Lakowski, M Baron, J Bainbridge, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
A recessive truncating variant in thrombospondin-1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous familyHanadi A Abdelrahman, Aisha Al-Shamsi, Anne John, et al.
BMC Medical Genetics|February 27, 2010
Molecular and clinical analysis of Ellis-van Creveld syndrome in the United Arab EmiratesBassam R Ali, Nadia A Akawi, Faris Chedid, et al.
Pageof 120

Showing results (631-640 of 1,192) with videos related to

Sort By:
Pageof 120
Biorxiv : the Preprint Server for Biology|December 15, 2025
DNA extraction and virome processing methods strongly influence recovered human gut viral community characteristicsLuke S Hillary, Trina A Knotts, Sean H Adams, et al.
Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|March 4, 2026
Pregnancy after bariatric surgery: persistent obesity and longer time to conception influences peripartum outcomes more than the type of operationMiaoli E Bloemhard, Ariana A Schmulbach, Kanksha Koti, et al.
Frontiers in Physiology|January 25, 2021
<i>Ex vivo</i> Methods for Measuring Cardiac Muscle Mechanical PropertiesWalter E Knight, Hadi R Ali, Stephanie J Nakano, et al.
Neuroradiology|September 20, 2006
Tumor lysis syndrome as a contributory factor to the development of reversible posterior leukoencephalopathyA Ozkan, B Hakyemez, F Ozkalemkas, et al.
Annals of Surgery|October 31, 2013
Single-site robotic cholecystectomy in a broadly inclusive patient population: a prospective studyTamas J Vidovszky, Aaron D Carr, Gina N Farinholt, et al.
AIDS (London, England)|July 1, 1991
HIV prevalence and risk behaviours for HIV transmission in South Australian prisonsM D Gaughwin, R M Douglas, C Liew, et al.
Clinical Endocrinology|August 21, 2023
The I-CAH Registry: A platform for international collaboration for improving knowledge and clinical care in congenital adrenal hyperplasiaXanthippi Tseretopoulou, Jillian Bryce, Minglu Chen, et al.
Human Molecular Genetics|September 23, 2010
Cone and rod photoreceptor transplantation in models of the childhood retinopathy Leber congenital amaurosis using flow-sorted Crx-positive donor cellsJ Lakowski, M Baron, J Bainbridge, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
A recessive truncating variant in thrombospondin-1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous familyHanadi A Abdelrahman, Aisha Al-Shamsi, Anne John, et al.
BMC Medical Genetics|February 27, 2010
Molecular and clinical analysis of Ellis-van Creveld syndrome in the United Arab EmiratesBassam R Ali, Nadia A Akawi, Faris Chedid, et al.
Pageof 120