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Bodo B Beck

Showing results (11-20 of 105) with videos related to

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Pediatric Nephrology (Berlin, Germany)|July 17, 2017
Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type IIIAda Ventzke, Markus Feldkötter, Andrew Wei, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 11, 2011
Respiratory and general outcome in neonates with renal oligohydramnios--a single-centre experienceKatrin Mehler, Bodo B Beck, Ingrid Kaul, et al.
Pediatric Nephrology (Berlin, Germany)|June 13, 2016
Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entityBodo B Beck, FrancJan van Spronsen, Arjan Diepstra, et al.
Frontiers in Pediatrics|March 29, 2020
Case Report: Exome Sequencing Reveals LRBA Deficiency in a Patient With End-Stage Renal DiseaseChristina Taylan, Andrea Wenzel, Florian Erger, et al.
HGG Advances|April 2, 2025
Severe Joubert syndrome in family with homozygous POC1B p.Arg106Pro variant is due to a co-inherited deep-intronic mutation in the neighboring CEP290 geneChristian Betz, Björn Reusch, Thomas Langmann, et al.
The American Journal of Case Reports|February 2, 2021
Four Cases of Maturity Onset Diabetes of the Young (MODY) Type 5 Associated with Mutations in the Hepatocyte Nuclear Factor 1 Beta (HNF1B) Gene Presenting in a 13-Year-Old Boy and in Adult Men Aged 33, 34, and 35 Years in PolandRafał Motyka, Marcin Kołbuc, Wojciech Wierzchołowski, et al.
Pediatric Nephrology (Berlin, Germany)|August 16, 2003
Urinary NAG in children with urolithiasis, nephrocalcinosis, or risk of urolithiasisPrzemyslaw Sikora, Sara Glatz, Bodo B Beck, et al.
Proteomics|February 14, 2018
Autosomal Tubulointerstitial Kidney Disease-MUC1 Type: Differential Proteomics Suggests that Mutated MUC1 (insC) Affects Vesicular Transport in Renal Epithelial CellsSimon Staubach, Andrea Wenzel, Bodo B Beck, et al.
Kidney International|June 19, 2008
The case: A boy with recurrent stonesBodo B Beck, Norbert Laube, Sandra Habbig, et al.
Circulation. Heart Failure|July 18, 2013
Apical sparing of longitudinal strain, left ventricular rotational abnormalities, and short-axis dysfunction in primary hyperoxaluria type 1Ruth Lagies, Bodo B Beck, Bernd Hoppe, et al.
Pageof 11

Showing results (11-20 of 105) with videos related to

Sort By:
Pageof 11
Pediatric Nephrology (Berlin, Germany)|July 17, 2017
Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type IIIAda Ventzke, Markus Feldkötter, Andrew Wei, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 11, 2011
Respiratory and general outcome in neonates with renal oligohydramnios--a single-centre experienceKatrin Mehler, Bodo B Beck, Ingrid Kaul, et al.
Pediatric Nephrology (Berlin, Germany)|June 13, 2016
Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entityBodo B Beck, FrancJan van Spronsen, Arjan Diepstra, et al.
Frontiers in Pediatrics|March 29, 2020
Case Report: Exome Sequencing Reveals LRBA Deficiency in a Patient With End-Stage Renal DiseaseChristina Taylan, Andrea Wenzel, Florian Erger, et al.
HGG Advances|April 2, 2025
Severe Joubert syndrome in family with homozygous POC1B p.Arg106Pro variant is due to a co-inherited deep-intronic mutation in the neighboring CEP290 geneChristian Betz, Björn Reusch, Thomas Langmann, et al.
The American Journal of Case Reports|February 2, 2021
Four Cases of Maturity Onset Diabetes of the Young (MODY) Type 5 Associated with Mutations in the Hepatocyte Nuclear Factor 1 Beta (HNF1B) Gene Presenting in a 13-Year-Old Boy and in Adult Men Aged 33, 34, and 35 Years in PolandRafał Motyka, Marcin Kołbuc, Wojciech Wierzchołowski, et al.
Pediatric Nephrology (Berlin, Germany)|August 16, 2003
Urinary NAG in children with urolithiasis, nephrocalcinosis, or risk of urolithiasisPrzemyslaw Sikora, Sara Glatz, Bodo B Beck, et al.
Proteomics|February 14, 2018
Autosomal Tubulointerstitial Kidney Disease-MUC1 Type: Differential Proteomics Suggests that Mutated MUC1 (insC) Affects Vesicular Transport in Renal Epithelial CellsSimon Staubach, Andrea Wenzel, Bodo B Beck, et al.
Kidney International|June 19, 2008
The case: A boy with recurrent stonesBodo B Beck, Norbert Laube, Sandra Habbig, et al.
Circulation. Heart Failure|July 18, 2013
Apical sparing of longitudinal strain, left ventricular rotational abnormalities, and short-axis dysfunction in primary hyperoxaluria type 1Ruth Lagies, Bodo B Beck, Bernd Hoppe, et al.
Pageof 11