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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 characteristics
Luke 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 operation
Miaoli 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 Properties
Walter 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 leukoencephalopathy
A 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 study
Tamas 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 prisons
M 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 hyperplasia
Xanthippi 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 cells
J 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 family
Hanadi 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 Emirates
Bassam R Ali, Nadia A Akawi, Faris Chedid, et al.
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Search research articles
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Showing results (631-640 of 1,192) with videos related to
Sort By:
Page
of 120
Biorxiv : the Preprint Server for Biology
|
December 15, 2025
DNA extraction and virome processing methods strongly influence recovered human gut viral community characteristics
Luke 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 operation
Miaoli 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 Properties
Walter 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 leukoencephalopathy
A 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 study
Tamas 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 prisons
M 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 hyperplasia
Xanthippi 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 cells
J 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 family
Hanadi 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 Emirates
Bassam R Ali, Nadia A Akawi, Faris Chedid, et al.
Page
of 120