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Braunisch

Showing results (41-50 of 80) with videos related to

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Frontiers in Genetics|June 14, 2021
Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic TestingMichaela Stippel, Korbinian M Riedhammer, Bärbel Lange-Sperandio, et al.
Scientific Reports|April 30, 2021
Application of regularized regression to identify novel predictors of mortality in a cohort of hemodialysis patientsStanislas Werfel, Georg Lorenz, Bernhard Haller, et al.
European Archives of Psychiatry and Clinical Neuroscience|October 8, 2025
Correction: All eyes on PCS: analysis of the retinal microvasculature in patients with post-COVID syndrome-study protocol of a 1 year prospective case-control studyTimon Kuchler, Renate Hausinger, Matthias C Braunisch, et al.
European Archives of Psychiatry and Clinical Neuroscience|December 2, 2023
All eyes on PCS: analysis of the retinal microvasculature in patients with post-COVID syndrome-study protocol of a 1 year prospective case-control studyTimon Kuchler, Renate Hausinger, Matthias C Braunisch, et al.
Frontiers in Pediatrics|June 28, 2018
Heterozygous <i>COL4A3</i> Variants in Histologically Diagnosed Focal Segmental GlomerulosclerosisMatthias C Braunisch, Maike Büttner-Herold, Roman Günthner, et al.
Scientific Reports|June 17, 2024
Endothelial dysfunction in retinal vessels of hemodialysis patients compared to healthy controlsRoman Günthner, Georg Lorenz, Matthias Christoph Braunisch, et al.
Clinical Kidney Journal|July 26, 2024
Measures of wave intensity as a non-invasive surrogate for cardiac function predicts mortality in haemodialysis patientsChristopher C Mayer, Pantelis A Sarafidis, Julia Matschkal, et al.
European Journal of Human Genetics : EJHG|September 5, 2020
Identification of disease-causing variants by comprehensive genetic testing with exome sequencing in adults with suspicion of hereditary FSGSMatthias Christoph Braunisch, Korbinian Maria Riedhammer, Pierre-Maurice Herr, et al.
Clinical Genetics|January 12, 2024
Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4?Korbinian M Riedhammer, Hannes Simmendinger, Velibor Tasic, et al.
BMJ Open|April 22, 2022
Study protocol: the TRAnsplant BIOpsies (TRABIO) study - a prospective, observational, multicentre cohort study to assess the treatment of kidney graft rejectionsFriedrich Alexander von Samson-Himmelstjerna, Grit Esser, Kevin Schulte, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Frontiers in Genetics|June 14, 2021
Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic TestingMichaela Stippel, Korbinian M Riedhammer, Bärbel Lange-Sperandio, et al.
Scientific Reports|April 30, 2021
Application of regularized regression to identify novel predictors of mortality in a cohort of hemodialysis patientsStanislas Werfel, Georg Lorenz, Bernhard Haller, et al.
European Archives of Psychiatry and Clinical Neuroscience|October 8, 2025
Correction: All eyes on PCS: analysis of the retinal microvasculature in patients with post-COVID syndrome-study protocol of a 1 year prospective case-control studyTimon Kuchler, Renate Hausinger, Matthias C Braunisch, et al.
European Archives of Psychiatry and Clinical Neuroscience|December 2, 2023
All eyes on PCS: analysis of the retinal microvasculature in patients with post-COVID syndrome-study protocol of a 1 year prospective case-control studyTimon Kuchler, Renate Hausinger, Matthias C Braunisch, et al.
Frontiers in Pediatrics|June 28, 2018
Heterozygous <i>COL4A3</i> Variants in Histologically Diagnosed Focal Segmental GlomerulosclerosisMatthias C Braunisch, Maike Büttner-Herold, Roman Günthner, et al.
Scientific Reports|June 17, 2024
Endothelial dysfunction in retinal vessels of hemodialysis patients compared to healthy controlsRoman Günthner, Georg Lorenz, Matthias Christoph Braunisch, et al.
Clinical Kidney Journal|July 26, 2024
Measures of wave intensity as a non-invasive surrogate for cardiac function predicts mortality in haemodialysis patientsChristopher C Mayer, Pantelis A Sarafidis, Julia Matschkal, et al.
European Journal of Human Genetics : EJHG|September 5, 2020
Identification of disease-causing variants by comprehensive genetic testing with exome sequencing in adults with suspicion of hereditary FSGSMatthias Christoph Braunisch, Korbinian Maria Riedhammer, Pierre-Maurice Herr, et al.
Clinical Genetics|January 12, 2024
Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4?Korbinian M Riedhammer, Hannes Simmendinger, Velibor Tasic, et al.
BMJ Open|April 22, 2022
Study protocol: the TRAnsplant BIOpsies (TRABIO) study - a prospective, observational, multicentre cohort study to assess the treatment of kidney graft rejectionsFriedrich Alexander von Samson-Himmelstjerna, Grit Esser, Kevin Schulte, et al.
Pageof 8