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Jan Halbritter

Showing results (1-10 of 117) with videos related to

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Kidney International|October 20, 2023
Urinary stone disease: closing the heritability gap by challenging conventional Mendelian inheritanceJan Halbritter
Nephrologie & Therapeutique|April 29, 2021
Genetics of kidney stone disease-Polygenic meets monogenicJan Halbritter
BJU International|April 12, 2021
'Case of the Month' from the University Medicine Mannheim: managing a complex stone patient with recurrent stone formationThomas Knoll, Jan Halbritter
Kidney International|February 23, 2026
Phenotype first: a data-driven approach to genetic penetranceJan Halbritter, Eric Olinger
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 19, 2026
Genetic testing in chronic kidney disease of uneXplained cause (CKDx): clinical insights and evolving diagnostic paradigmsJan Halbritter, Matias Simons
Kidney International Reports|September 18, 2024
Sporadic ADPKD<i>-IFT140</i>: Absence of Family History as an Indicator of Clinical MildnessManuel A Anderegg, Jan Halbritter
Current Opinion in Nephrology and Hypertension|January 19, 2024
The genetics of cystinuria - an update and critical reevaluationClàudia Abad Baucells, Ria Schönauer, Jan Halbritter
Nutrients|July 11, 2023
Clinical and Functional Assessment of Digenicity in Renal Phosphate WastingFriederike Petzold, Ria Schönauer, Andreas Werner, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 12, 2025
CKDx: Simplicity matters, implementation is keyEmilie Cornec-Le Gall, Jan Halbritter, Roman Ulrich Müller
Metabolism: Clinical and Experimental|February 6, 2008
Phenotype of a patient with a de novo mutation in the hepatocyte nuclear factor 1beta/maturity-onset diabetes of the young type 5 geneChristof Mayer, Yvonne Böttcher, Peter Kovacs, et al.
Pageof 12

Showing results (1-10 of 117) with videos related to

Sort By:
Pageof 12
Kidney International|October 20, 2023
Urinary stone disease: closing the heritability gap by challenging conventional Mendelian inheritanceJan Halbritter
Nephrologie & Therapeutique|April 29, 2021
Genetics of kidney stone disease-Polygenic meets monogenicJan Halbritter
BJU International|April 12, 2021
'Case of the Month' from the University Medicine Mannheim: managing a complex stone patient with recurrent stone formationThomas Knoll, Jan Halbritter
Kidney International|February 23, 2026
Phenotype first: a data-driven approach to genetic penetranceJan Halbritter, Eric Olinger
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 19, 2026
Genetic testing in chronic kidney disease of uneXplained cause (CKDx): clinical insights and evolving diagnostic paradigmsJan Halbritter, Matias Simons
Kidney International Reports|September 18, 2024
Sporadic ADPKD<i>-IFT140</i>: Absence of Family History as an Indicator of Clinical MildnessManuel A Anderegg, Jan Halbritter
Current Opinion in Nephrology and Hypertension|January 19, 2024
The genetics of cystinuria - an update and critical reevaluationClàudia Abad Baucells, Ria Schönauer, Jan Halbritter
Nutrients|July 11, 2023
Clinical and Functional Assessment of Digenicity in Renal Phosphate WastingFriederike Petzold, Ria Schönauer, Andreas Werner, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 12, 2025
CKDx: Simplicity matters, implementation is keyEmilie Cornec-Le Gall, Jan Halbritter, Roman Ulrich Müller
Metabolism: Clinical and Experimental|February 6, 2008
Phenotype of a patient with a de novo mutation in the hepatocyte nuclear factor 1beta/maturity-onset diabetes of the young type 5 geneChristof Mayer, Yvonne Böttcher, Peter Kovacs, et al.
Pageof 12