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Avram Z Traum

Showing results (21-30 of 34) with videos related to

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Pediatric Transplantation|January 6, 2023
Equity factors in pediatric transplant listing: Initial findings from a single center reviewDawn Freiberger, Brendan Kimball, Avram Z Traum, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patientsAngela E Lin, Avram Z Traum, Inderneel Sahai, et al.
Pediatric Nephrology (Berlin, Germany)|June 2, 2022
Survival of neonates born with kidney failure during the initial hospitalizationDonna J Claes, Troy Richardson, Matthew W Harer, et al.
Pediatric Transplantation|December 30, 2021
Outcomes of granulocyte colony-stimulating factor use in pediatric kidney transplant recipients: A Pediatric Nephrology Research Consortium studyRachel M Engen, Patricia L Weng, Weiwen Shih, et al.
JIMD Reports|November 15, 2024
Reduced guanidinoacetate in plasma of patients with autosomal dominant Fanconi syndrome due to heterozygous P341L <i>GATM</i> variant and study of organoids towards treatmentIgnacio Portales-Castillo, Rhea Singal, Anastasia Ambrose, et al.
Kidney International Reports|August 19, 2024
Derivation and Validation of an Optimal Neutrophil Gelatinase-Associated Lipocalin Cutoff to Predict Stage 2/3 Acute Kidney Injury (AKI) in Critically Ill ChildrenStuart L Goldstein, Ayse Akcan-Arikan, Natasha Afonso, et al.
Hypertension (Dallas, Tex. : 1979)|February 28, 2018
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeJillian K Warejko, Markus Schueler, Asaf Vivante, et al.
Journal of the American Society of Nephrology : JASN|January 19, 2019
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant RecipientsNina Mann, Daniela A Braun, Kassaundra Amann, et al.
Kidney International|September 13, 2017
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosisAnkana Daga, Amar J Majmundar, Daniela A Braun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Pediatric Transplantation|January 6, 2023
Equity factors in pediatric transplant listing: Initial findings from a single center reviewDawn Freiberger, Brendan Kimball, Avram Z Traum, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patientsAngela E Lin, Avram Z Traum, Inderneel Sahai, et al.
Pediatric Nephrology (Berlin, Germany)|June 2, 2022
Survival of neonates born with kidney failure during the initial hospitalizationDonna J Claes, Troy Richardson, Matthew W Harer, et al.
Pediatric Transplantation|December 30, 2021
Outcomes of granulocyte colony-stimulating factor use in pediatric kidney transplant recipients: A Pediatric Nephrology Research Consortium studyRachel M Engen, Patricia L Weng, Weiwen Shih, et al.
JIMD Reports|November 15, 2024
Reduced guanidinoacetate in plasma of patients with autosomal dominant Fanconi syndrome due to heterozygous P341L <i>GATM</i> variant and study of organoids towards treatmentIgnacio Portales-Castillo, Rhea Singal, Anastasia Ambrose, et al.
Kidney International Reports|August 19, 2024
Derivation and Validation of an Optimal Neutrophil Gelatinase-Associated Lipocalin Cutoff to Predict Stage 2/3 Acute Kidney Injury (AKI) in Critically Ill ChildrenStuart L Goldstein, Ayse Akcan-Arikan, Natasha Afonso, et al.
Hypertension (Dallas, Tex. : 1979)|February 28, 2018
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeJillian K Warejko, Markus Schueler, Asaf Vivante, et al.
Journal of the American Society of Nephrology : JASN|January 19, 2019
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant RecipientsNina Mann, Daniela A Braun, Kassaundra Amann, et al.
Kidney International|September 13, 2017
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosisAnkana Daga, Amar J Majmundar, Daniela A Braun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Pageof 4