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Katrin Hahn

Showing results (71-80 of 78) with videos related to

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Annals of Medicine|October 18, 2021
Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiologyVolha Skrahina, Ulrike Grittner, Christian Beetz, et al.
Journal of Clinical Medicine|October 26, 2024
Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 ParticipantsSabine Rösner, Luba M Pardo, Aida M Bertoli-Avella, et al.
Journal of the Neurological Sciences|September 5, 2025
The expanding clinical utility of blood neurofilament light chain (bNfL): a multi-disciplinary diagnostic toolPeter Körtvelyessy, Burak Arslan, Jonah Nietiet, et al.
Brain : a Journal of Neurology|April 7, 2025
Mitochondrial damage is associated with an early immune response in inclusion body myositisFelix Kleefeld, Emily Cross, Daniel Lagos, et al.
ESC Heart Failure|November 6, 2024
Real-world characteristics and treatment of cardiac transthyretin amyloidosis: A multicentre, observational studyRichard J Nies, Svenja Ney, Ingrid Kindermann, et al.
Plos One|June 2, 2026
On the crossroads of interdisciplinary medicine in amyloidosis - study protocol for a single-center interdisciplinary registry studyHelena Pernice, Gina Barzen, Jakub Piwowarski, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|January 26, 2026
Current treatment decisions in cardiac transthyretin amyloidosis: a multicentre analysisDaniel Lavall, Katharina Knoll, Sebastian Spethmann, et al.
Brain : a Journal of Neurology|February 12, 2025
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORDAndrea Cortese, Maike F Dohrn, Riccardo Curro, et al.
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Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Annals of Medicine|October 18, 2021
Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiologyVolha Skrahina, Ulrike Grittner, Christian Beetz, et al.
Journal of Clinical Medicine|October 26, 2024
Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 ParticipantsSabine Rösner, Luba M Pardo, Aida M Bertoli-Avella, et al.
Journal of the Neurological Sciences|September 5, 2025
The expanding clinical utility of blood neurofilament light chain (bNfL): a multi-disciplinary diagnostic toolPeter Körtvelyessy, Burak Arslan, Jonah Nietiet, et al.
Brain : a Journal of Neurology|April 7, 2025
Mitochondrial damage is associated with an early immune response in inclusion body myositisFelix Kleefeld, Emily Cross, Daniel Lagos, et al.
ESC Heart Failure|November 6, 2024
Real-world characteristics and treatment of cardiac transthyretin amyloidosis: A multicentre, observational studyRichard J Nies, Svenja Ney, Ingrid Kindermann, et al.
Plos One|June 2, 2026
On the crossroads of interdisciplinary medicine in amyloidosis - study protocol for a single-center interdisciplinary registry studyHelena Pernice, Gina Barzen, Jakub Piwowarski, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|January 26, 2026
Current treatment decisions in cardiac transthyretin amyloidosis: a multicentre analysisDaniel Lavall, Katharina Knoll, Sebastian Spethmann, et al.
Brain : a Journal of Neurology|February 12, 2025
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORDAndrea Cortese, Maike F Dohrn, Riccardo Curro, et al.
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