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Michael C Braun

Showing results (41-50 of 55) with videos related to

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Journal of the American Heart Association|February 21, 2020
<i>Stim1</i> Polymorphism Disrupts Immune Signaling and Creates Renal Injury in HypertensionIsha S Dhande, Yaming Zhu, Sterling C Kneedler, et al.
Circulation. Cardiovascular Genetics|November 5, 2014
Hypertensive renal injury is associated with gene variation affecting immune signalingMichael C Braun, Stacy M Herring, Nisha Gokul, et al.
Plos One|August 10, 2017
Regional citrate anticoagulation for continuous renal replacement therapy in pediatric patients with liver failureKeila Rodriguez, Poyyapakkam R Srivaths, Leyat Tal, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 19, 2021
Novel scoring system for determining fetal candidacy for prenatal intervention for severe congenital lower urinary tract obstructionAhmed A Nassr, Hadi Erfani, Jimmy Espinoza, et al.
Pediatric Nephrology (Berlin, Germany)|August 13, 2021
The effect of continuous venovenous hemodiafiltration on amino acid delivery, clearance, and removal in childrenRichard P Lion, Molly R Vega, E O'Brien Smith, et al.
Prenatal Diagnosis|March 15, 2023
Fetal bladder morphology as a predictor of outcome in fetal lower urinary tract obstructionKara J Shannon, Sarah VanLoh, Jimmy Espinoza, et al.
Journal of Clinical Immunology|April 7, 2016
Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory DiseaseTimothy J Vece, Levi B Watkin, Sarah Nicholas, et al.
Pediatric Nephrology (Berlin, Germany)|November 4, 2015
Defining and predicting 'intrauterine fetal renal failure' in congenital lower urinary tract obstructionRodrigo Ruano, Adnan Safdar, Jason Au, et al.
Prenatal Diagnosis|June 2, 2016
Factors associated with fetal shunt dislodgement in lower urinary tract obstructionMichael P Kurtz, Chester J Koh, Grace Anne Jamail, et al.
Molecular Genetics & Genomic Medicine|October 1, 2019
Characterization of the renal phenotype in RMND1-related mitochondrial diseaseBrian J Shayota, Nhon T Le, Nasim Bekheirnia, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Journal of the American Heart Association|February 21, 2020
<i>Stim1</i> Polymorphism Disrupts Immune Signaling and Creates Renal Injury in HypertensionIsha S Dhande, Yaming Zhu, Sterling C Kneedler, et al.
Circulation. Cardiovascular Genetics|November 5, 2014
Hypertensive renal injury is associated with gene variation affecting immune signalingMichael C Braun, Stacy M Herring, Nisha Gokul, et al.
Plos One|August 10, 2017
Regional citrate anticoagulation for continuous renal replacement therapy in pediatric patients with liver failureKeila Rodriguez, Poyyapakkam R Srivaths, Leyat Tal, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 19, 2021
Novel scoring system for determining fetal candidacy for prenatal intervention for severe congenital lower urinary tract obstructionAhmed A Nassr, Hadi Erfani, Jimmy Espinoza, et al.
Pediatric Nephrology (Berlin, Germany)|August 13, 2021
The effect of continuous venovenous hemodiafiltration on amino acid delivery, clearance, and removal in childrenRichard P Lion, Molly R Vega, E O'Brien Smith, et al.
Prenatal Diagnosis|March 15, 2023
Fetal bladder morphology as a predictor of outcome in fetal lower urinary tract obstructionKara J Shannon, Sarah VanLoh, Jimmy Espinoza, et al.
Journal of Clinical Immunology|April 7, 2016
Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory DiseaseTimothy J Vece, Levi B Watkin, Sarah Nicholas, et al.
Pediatric Nephrology (Berlin, Germany)|November 4, 2015
Defining and predicting 'intrauterine fetal renal failure' in congenital lower urinary tract obstructionRodrigo Ruano, Adnan Safdar, Jason Au, et al.
Prenatal Diagnosis|June 2, 2016
Factors associated with fetal shunt dislodgement in lower urinary tract obstructionMichael P Kurtz, Chester J Koh, Grace Anne Jamail, et al.
Molecular Genetics & Genomic Medicine|October 1, 2019
Characterization of the renal phenotype in RMND1-related mitochondrial diseaseBrian J Shayota, Nhon T Le, Nasim Bekheirnia, et al.
Pageof 6