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Bodo B Beck

Showing results (51-60 of 105) with videos related to

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Pediatric Nephrology (Berlin, Germany)|April 2, 2017
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutationsKathrin Ebner, Claudia Dafinger, Nadina Ortiz-Bruechle, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 13, 2022
Lifelong effect of therapy in young patients with the COL4A5 Alport missense variant p.(Gly624Asp): a prospective cohort studyJan Boeckhaus, Julia Hoefele, Korbinian M Riedhammer, et al.
Kidney International|April 18, 2021
A report from the European Hyperoxaluria Consortium (OxalEurope) Registry on a large cohort of patients with primary hyperoxaluria type 3Cristina Martin-Higueras, Sander F Garrelfs, Jaap W Groothoff, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 23, 2021
Arterial Hypertension in a 10-Year-Old GirlAlina Meeser, Bodo B Beck, Martin Dübbers, et al.
Journal of Clinical Medicine|August 7, 2021
Hyperuricemia Is an Early and Relatively Common Feature in Children with <i>HNF1B</i> Nephropathy but Its Utility as a Predictor of the Disease Is LimitedMarcin Kołbuc, Beata Bieniaś, Sandra Habbig, et al.
BMC Medical Genetics|May 14, 2017
Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancerMalte P Bartram, Tripti Mishra, Nadine Reintjes, et al.
Kidney International|June 21, 2021
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathyJohannes Birtel, Georg Spital, Marius Book, et al.
Genome Medicine|June 26, 2020
cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNAFlorian Erger, Deborah Nörling, Domenica Borchert, et al.
Journal of Proteomics|November 14, 2021
MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cellsBjörn Reusch, Malte P Bartram, Claudia Dafinger, et al.
Plos One|October 15, 2013
A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotypeJan Hauke, Andrea Schild, Antje Neugebauer, et al.
Pageof 11

Showing results (51-60 of 105) with videos related to

Sort By:
Pageof 11
Pediatric Nephrology (Berlin, Germany)|April 2, 2017
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutationsKathrin Ebner, Claudia Dafinger, Nadina Ortiz-Bruechle, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 13, 2022
Lifelong effect of therapy in young patients with the COL4A5 Alport missense variant p.(Gly624Asp): a prospective cohort studyJan Boeckhaus, Julia Hoefele, Korbinian M Riedhammer, et al.
Kidney International|April 18, 2021
A report from the European Hyperoxaluria Consortium (OxalEurope) Registry on a large cohort of patients with primary hyperoxaluria type 3Cristina Martin-Higueras, Sander F Garrelfs, Jaap W Groothoff, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 23, 2021
Arterial Hypertension in a 10-Year-Old GirlAlina Meeser, Bodo B Beck, Martin Dübbers, et al.
Journal of Clinical Medicine|August 7, 2021
Hyperuricemia Is an Early and Relatively Common Feature in Children with <i>HNF1B</i> Nephropathy but Its Utility as a Predictor of the Disease Is LimitedMarcin Kołbuc, Beata Bieniaś, Sandra Habbig, et al.
BMC Medical Genetics|May 14, 2017
Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancerMalte P Bartram, Tripti Mishra, Nadine Reintjes, et al.
Kidney International|June 21, 2021
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathyJohannes Birtel, Georg Spital, Marius Book, et al.
Genome Medicine|June 26, 2020
cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNAFlorian Erger, Deborah Nörling, Domenica Borchert, et al.
Journal of Proteomics|November 14, 2021
MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cellsBjörn Reusch, Malte P Bartram, Claudia Dafinger, et al.
Plos One|October 15, 2013
A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotypeJan Hauke, Andrea Schild, Antje Neugebauer, et al.
Pageof 11