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Jonas Wixner

11PUBLICATIONS
43CO-AUTHORS
Gene and molecular therapyNeurology and neuromuscular diseasesPanel data analysisAutonomic nervous systemCentral nervous system
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Journal

Publications (11)

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|Jul 09, 2026
Guidelines for the management of hereditary ATTR amyloidosis 2026.

|Jun 08, 2026
Evaluation of serum neurofilament light chain, GFAP, and peripherin as biomarkers in hereditary transthyretin amyloidosis.

|Apr 06, 2026
Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy: An Exploratory Analysis of Treatment Effect in Male and Female Patients.

Márcia Waddington Cruz, John L Berk, Yeşim Parman

|Jul 27, 2025
Introducing a revised version of the Kumamoto scale as an easy-to-use clinical tool for monitoring multisystemic changes in hereditary transthyretin amyloidosis.

Jonas Wixner, Björn Pilebro, Tale N Wien

|May 25, 2025
Cognitive manifestations and brain integrity in hereditary transthyretin amyloidosis: a systematic review.

Iara Senem, Rodrigo Melo Conde, Maria Paula Foss

|Nov 05, 2024
Exploring cognitive functions and brain structure in Hereditary Transthyretin amyloidosis using brain MRI and neuropsychological assessment.

Iara Senem, Maria Paula Foss, Carolina Lavigne-Moreira

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Frequent Collaborators

2 joint publications

Intissar Anan

2 joint publications

John L Berk

2 joint publications

Mathew S Maurer

2 joint publications

Markus Weiler

2 joint publications

Márcia Waddington Cruz

2 joint publications

Iara Senem

2 joint publications

Maria Paula Foss

2 joint publications

Wilson Marques

2 joint publications

Jan Axelsson

1 joint publications

Giampaolo Merlini

Frequent Collaborators

2 joint publications

Intissar Anan

2 joint publications

John L Berk

2 joint publications

Mathew S Maurer

2 joint publications

Markus Weiler