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Bodo B Beck

Showing results (41-50 of 105) with videos related to

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Stem Cell Research|November 13, 2019
Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT geneRebeca Martinez-Turrillas, Saray Rodriguez-Diaz, Paula Rodriguez-Marquez, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 20, 2018
Translation inhibition corrects aberrant localization of mutant alanine-glyoxylate aminotransferase: possible therapeutic approach for hyperoxaluriaRuth Belostotsky, Roman Lyakhovetsky, Michael Y Sherman, et al.
Clinical Nephrology|May 16, 2017
A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome
Kathrin Ebner, Nadine Reintjes, Markus Feldkötter, et al.
Kidney International Reports|January 15, 2025
Effective Newborn Screening for Type 1 and 3 Primary HyperoxaluriaBernd Hoppe, Cristina Martin-Higueras, Lodovica Borghese, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 31, 2012
Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?Bodo B Beck, Sandra Habbig, Katalin Dittrich, et al.
Journal of the American Society of Nephrology : JASN|April 3, 2016
Mucin-1 Increases Renal TRPV5 Activity In Vitro, and Urinary Level Associates with Calcium Nephrolithiasis in PatientsMingzhu Nie, Manjot S Bal, Zhufeng Yang, et al.
Pediatric Nephrology (Berlin, Germany)|January 14, 2017
Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalitiesAgnes Hackl, Katrin Mehler, Ingo Gottschalk, et al.
Polish Archives of Internal Medicine|December 4, 2020
Still diagnosed too late and under-recognized? The first comprehensive report on primary hyperoxaluria in PolandPrzemysław Sikora, Marcin Zaniew, Ryszard Grenda, et al.
Polish Archives of Internal Medicine|August 23, 2022
Nephropathic cystinosis in Poland: a 40-year retrospective studyPrzemysław Sikora, Ryszard Grenda, Małgorzata Kowalczyk, et al.
Journal of Inherited Metabolic Disease|February 14, 2025
C1GALT1C1-Associated Mosaic Disorder of Glycosylation in a FemaleRajindra P Aryal, Aditya Ramanujan, Camille Bucci, et al.
Pageof 11

Showing results (41-50 of 105) with videos related to

Sort By:
Pageof 11
Stem Cell Research|November 13, 2019
Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT geneRebeca Martinez-Turrillas, Saray Rodriguez-Diaz, Paula Rodriguez-Marquez, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 20, 2018
Translation inhibition corrects aberrant localization of mutant alanine-glyoxylate aminotransferase: possible therapeutic approach for hyperoxaluriaRuth Belostotsky, Roman Lyakhovetsky, Michael Y Sherman, et al.
Clinical Nephrology|May 16, 2017
A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome
Kathrin Ebner, Nadine Reintjes, Markus Feldkötter, et al.
Kidney International Reports|January 15, 2025
Effective Newborn Screening for Type 1 and 3 Primary HyperoxaluriaBernd Hoppe, Cristina Martin-Higueras, Lodovica Borghese, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 31, 2012
Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?Bodo B Beck, Sandra Habbig, Katalin Dittrich, et al.
Journal of the American Society of Nephrology : JASN|April 3, 2016
Mucin-1 Increases Renal TRPV5 Activity In Vitro, and Urinary Level Associates with Calcium Nephrolithiasis in PatientsMingzhu Nie, Manjot S Bal, Zhufeng Yang, et al.
Pediatric Nephrology (Berlin, Germany)|January 14, 2017
Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalitiesAgnes Hackl, Katrin Mehler, Ingo Gottschalk, et al.
Polish Archives of Internal Medicine|December 4, 2020
Still diagnosed too late and under-recognized? The first comprehensive report on primary hyperoxaluria in PolandPrzemysław Sikora, Marcin Zaniew, Ryszard Grenda, et al.
Polish Archives of Internal Medicine|August 23, 2022
Nephropathic cystinosis in Poland: a 40-year retrospective studyPrzemysław Sikora, Ryszard Grenda, Małgorzata Kowalczyk, et al.
Journal of Inherited Metabolic Disease|February 14, 2025
C1GALT1C1-Associated Mosaic Disorder of Glycosylation in a FemaleRajindra P Aryal, Aditya Ramanujan, Camille Bucci, et al.
Pageof 11