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Florian Erger

Showing results (11-20 of 43) with videos related to

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Glycobiology|August 31, 2024
Cosmc regulates O-glycan extension in murine hepatocytesRajindra P Aryal, Maxence Noel, Junwei Zeng, 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.
Hypertension (Dallas, Tex. : 1979)|May 10, 2023
Disconnected Cardiac Autonomic Nerves in Genetic Ganglionic Acetylcholine Receptor Alpha-3 Subunit DeficiencyKarsten Heusser, Florian Erger, Ulrich Ebner, et al.
European Journal of Human Genetics : EJHG|December 3, 2024
ELMO2-related intraosseous vascular malformation: new cases with novel pathogenic variants, clinical follow-up and therapeutic approachesMert Karakaya, Iman Ragab, Vera Riehmer, et al.
European Journal of Human Genetics : EJHG|October 28, 2025
Correction: ELMO2-related intraosseous vascular malformation: new cases with novel pathogenic variants, clinical follow-up and therapeutic approachesMert Karakaya, Iman Ragab, Vera Riehmer, 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.
Clinical Kidney Journal|November 2, 2023
Copeptin in autosomal dominant polycystic kidney disease: real-world experiences from a large prospective cohort studySita Arjune, Simon Oehm, Polina Todorova, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 29, 2022
Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysisEsther Leenen, Florian Erger, Janine Altmüller, et al.
Clinical Nephrology|September 2, 2020
Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodiesAgnes Hackl, Florian Erger, Christine Skerka, 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.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Glycobiology|August 31, 2024
Cosmc regulates O-glycan extension in murine hepatocytesRajindra P Aryal, Maxence Noel, Junwei Zeng, 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.
Hypertension (Dallas, Tex. : 1979)|May 10, 2023
Disconnected Cardiac Autonomic Nerves in Genetic Ganglionic Acetylcholine Receptor Alpha-3 Subunit DeficiencyKarsten Heusser, Florian Erger, Ulrich Ebner, et al.
European Journal of Human Genetics : EJHG|December 3, 2024
ELMO2-related intraosseous vascular malformation: new cases with novel pathogenic variants, clinical follow-up and therapeutic approachesMert Karakaya, Iman Ragab, Vera Riehmer, et al.
European Journal of Human Genetics : EJHG|October 28, 2025
Correction: ELMO2-related intraosseous vascular malformation: new cases with novel pathogenic variants, clinical follow-up and therapeutic approachesMert Karakaya, Iman Ragab, Vera Riehmer, 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.
Clinical Kidney Journal|November 2, 2023
Copeptin in autosomal dominant polycystic kidney disease: real-world experiences from a large prospective cohort studySita Arjune, Simon Oehm, Polina Todorova, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 29, 2022
Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysisEsther Leenen, Florian Erger, Janine Altmüller, et al.
Clinical Nephrology|September 2, 2020
Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodiesAgnes Hackl, Florian Erger, Christine Skerka, 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.
Pageof 5