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Anna Bjerre

Showing results (51-60 of 77) with videos related to

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American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 15, 2020
Three-year outcomes from the CRADLE study in de novo pediatric kidney transplant recipients receiving everolimus with reduced tacrolimus and early steroid withdrawalBurkhard Tönshoff, Helio Tedesco-Silva, Robert Ettenger, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 23, 2012
Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tractElke Wühl, Karlijn J van Stralen, Enrico Verrina, et al.
Pediatric Nephrology (Berlin, Germany)|November 12, 2025
Changes in maintenance immunosuppression after pediatric kidney transplantation-a report from the Nordic pediatric kidney transplantation registryHenna Kaijansinkko, Juuso Tainio, Anna Bjerre, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 21, 2018
Early conversion of pediatric kidney transplant patients to everolimus with reduced tacrolimus and steroid elimination: Results of a randomized trialBurkhard Tönshoff, Robert Ettenger, Luca Dello Strologo, et al.
Kidney International Reports|November 29, 2023
Diagnostic Yield and Benefits of Whole Exome Sequencing in CAKUT Patients Diagnosed in the First Thousand Days of LifeLina Werfel, Helge Martens, Imke Hennies, et al.
European Journal of Human Genetics : EJHG|August 2, 2020
Rare heterozygous GDF6 variants in patients with renal anomaliesHelge Martens, Imke Hennies, Maike Getwan, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 2, 2013
Adult height in patients with advanced CKD requiring renal replacement therapy during childhoodJérôme Harambat, Marjolein Bonthuis, Karlijn J van Stralen, et al.
Lancet (London, England)|March 25, 2017
Mortality risk disparities in children receiving chronic renal replacement therapy for the treatment of end-stage renal disease across Europe: an ESPN-ERA/EDTA registry analysisNicholas C Chesnaye, Franz Schaefer, Marjolein Bonthuis, et al.
Human Molecular Genetics|March 24, 2017
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformationsAnne Kosfeld, Frank Brand, Anna-Carina Weiss, et al.
Human Genetics|September 6, 2022
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2Anne Christians, Esra Kesdiren, Imke Hennies, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 15, 2020
Three-year outcomes from the CRADLE study in de novo pediatric kidney transplant recipients receiving everolimus with reduced tacrolimus and early steroid withdrawalBurkhard Tönshoff, Helio Tedesco-Silva, Robert Ettenger, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 23, 2012
Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tractElke Wühl, Karlijn J van Stralen, Enrico Verrina, et al.
Pediatric Nephrology (Berlin, Germany)|November 12, 2025
Changes in maintenance immunosuppression after pediatric kidney transplantation-a report from the Nordic pediatric kidney transplantation registryHenna Kaijansinkko, Juuso Tainio, Anna Bjerre, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 21, 2018
Early conversion of pediatric kidney transplant patients to everolimus with reduced tacrolimus and steroid elimination: Results of a randomized trialBurkhard Tönshoff, Robert Ettenger, Luca Dello Strologo, et al.
Kidney International Reports|November 29, 2023
Diagnostic Yield and Benefits of Whole Exome Sequencing in CAKUT Patients Diagnosed in the First Thousand Days of LifeLina Werfel, Helge Martens, Imke Hennies, et al.
European Journal of Human Genetics : EJHG|August 2, 2020
Rare heterozygous GDF6 variants in patients with renal anomaliesHelge Martens, Imke Hennies, Maike Getwan, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 2, 2013
Adult height in patients with advanced CKD requiring renal replacement therapy during childhoodJérôme Harambat, Marjolein Bonthuis, Karlijn J van Stralen, et al.
Lancet (London, England)|March 25, 2017
Mortality risk disparities in children receiving chronic renal replacement therapy for the treatment of end-stage renal disease across Europe: an ESPN-ERA/EDTA registry analysisNicholas C Chesnaye, Franz Schaefer, Marjolein Bonthuis, et al.
Human Molecular Genetics|March 24, 2017
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformationsAnne Kosfeld, Frank Brand, Anna-Carina Weiss, et al.
Human Genetics|September 6, 2022
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2Anne Christians, Esra Kesdiren, Imke Hennies, et al.
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