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Gina Barzen on Muck Rack

Gina Barzen

As seen in: Nature, medRxiv
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Articles

Transferability of a US claims-based machine learning model for ATTRwt-CM identification: a retrospective evaluation in a German setting

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By Miriam R. Hübner, Isabel Mattig, Paul J. Wetzel, Helena F. Pernice, Gina Barzen, Nicolas Wieder, Jakub P. Piwowarski, Daniel R. Messroghli, Sebastian Spethmann, Richard Röttger, Josef Schepers, Katrin Hahn, Harisa Muratovic-Colic, Jan-Filip Rehburg, Katrin Wrede-Wihl, Stephan Bohl, Vera von Landenberg-Roberg
| Nature Verified
Abstract Cardiac amyloidosis (CA), a fatal and progressive cardiomyopathy is characterized by amyloid deposition within the myocardium. The main forms of CA include transthyretin amyloidosis (ATTR-CM; distinguished into a hereditary and wildtype form [ATTRv and ATTRwt]) and light-chain amyloidosis (AL). Transthyretin amyloidosis with cardiomyopathy (ATTR-CM) is increasingly recognized among heart failure (HF) patients, despite its underestimated prevalence as a rare disease.
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Wearables for Telemonitoring in ATTR-Amyloidosis: Current Perspectives

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By Andreas Kind, Helena F. Pernice, Gina Barzen
| preprints.org
You are already at the latest version Wearable sensors enable continuous recording of electrocardiographic, photoplethys-mographic, and inertial signals and have accelerated the development of digital bi-omarkers in cardiovascular medicine.
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Neurological affection and serum neurofilament light chain in wild type transthyretin amyloidosis - Scientific Reports

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By Helena F. Pernice, Carolin Herrmann, Gina Barzen, Elisabeth Blüthner, Fabian Knebel, Sebastian Spethmann, Bettina Heidecker, Christoph Wetz, Carsten Tschöpe, Adrian L. Knorz, Paul J. Wetzel, Finn Rieber, Eleonora Asaad
| Nature Verified
Abstract In contrast to inherited transthyretin amyloidosis (A-ATTRv), neuropathy is not a classic leading symptom of wild type transthyretin amyloidosis (A-ATTRwt). However, neurological symptoms are increasingly relevant in A-ATTRwt as well.
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