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Showing results (1191-1200 of 1,228) with videos related to

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Current Pediatric Reviews|June 24, 2022
Beta Thalassemia Carrier Rate: Problem Burden among High School ChildrenMohamed R El-Shanshory, Laila M Sherief, Sohier Yahia, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Clinical and Experimental Pediatrics|August 8, 2025
Serum copper and ceruloplasmin levels as biomarkers reflecting liver fibrosis in children with autoimmune hepatitisSalma Abdel Megeed Nagi, Mai Ibrahim Elashmawy, Amany E Elashkar, et al.
Nature|May 20, 2026
Mitochondrial L-2-hydroxyglutarate is a physiological signalling metaboliteRam P Chakrabarty, Jonathan G Van Vranken, Yuki Aoi, et al.
Nature Communications|October 22, 2015
Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilizationAlbane A Bizet, Anita Becker-Heck, Rebecca Ryan, et al.
American Journal of Human Genetics|November 24, 2020
DAAM2 Variants Cause Nephrotic Syndrome via Actin DysregulationRonen Schneider, Konstantin Deutsch, Gregory J Hoeprich, et al.
Circulation|September 1, 2020
Effect of Adding Ticagrelor to Standard Aspirin on Saphenous Vein Graft Patency in Patients Undergoing Coronary Artery Bypass Grafting (POPular CABG): A Randomized, Double-Blind, Placebo-Controlled TrialLaura M Willemsen, Paul W A Janssen, Joyce Peper, et al.
Nature Reviews. Nephrology|June 15, 2026
Clinical practice recommendations for the diagnosis and management of nephropathic cystinosisKatharina Hohenfellner, Elke Wühl, Dieter Haffner, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
A Phenotypic Paradigm for Cerebral Palsy GeneticsAdam S Arterbery, Michael A Gargano, Anita M Bagley, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndromeBshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Pageof 123

Showing results (1191-1200 of 1,228) with videos related to

Sort By:
Pageof 123
Current Pediatric Reviews|June 24, 2022
Beta Thalassemia Carrier Rate: Problem Burden among High School ChildrenMohamed R El-Shanshory, Laila M Sherief, Sohier Yahia, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Clinical and Experimental Pediatrics|August 8, 2025
Serum copper and ceruloplasmin levels as biomarkers reflecting liver fibrosis in children with autoimmune hepatitisSalma Abdel Megeed Nagi, Mai Ibrahim Elashmawy, Amany E Elashkar, et al.
Nature|May 20, 2026
Mitochondrial L-2-hydroxyglutarate is a physiological signalling metaboliteRam P Chakrabarty, Jonathan G Van Vranken, Yuki Aoi, et al.
Nature Communications|October 22, 2015
Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilizationAlbane A Bizet, Anita Becker-Heck, Rebecca Ryan, et al.
American Journal of Human Genetics|November 24, 2020
DAAM2 Variants Cause Nephrotic Syndrome via Actin DysregulationRonen Schneider, Konstantin Deutsch, Gregory J Hoeprich, et al.
Circulation|September 1, 2020
Effect of Adding Ticagrelor to Standard Aspirin on Saphenous Vein Graft Patency in Patients Undergoing Coronary Artery Bypass Grafting (POPular CABG): A Randomized, Double-Blind, Placebo-Controlled TrialLaura M Willemsen, Paul W A Janssen, Joyce Peper, et al.
Nature Reviews. Nephrology|June 15, 2026
Clinical practice recommendations for the diagnosis and management of nephropathic cystinosisKatharina Hohenfellner, Elke Wühl, Dieter Haffner, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
A Phenotypic Paradigm for Cerebral Palsy GeneticsAdam S Arterbery, Michael A Gargano, Anita M Bagley, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndromeBshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Pageof 123