Markus Weiler

26PUBLICATIONS

137CO-AUTHORS

Gene and molecular therapyPanel data analysisAutonomic nervous systemNeurology and neuromuscular diseasesNeurogenetics

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Publications (26)

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|Jul 09, 2026

Guidelines for the management of hereditary ATTR amyloidosis 2026.

|Jun 10, 2026

First-Generation TTR Silencing Therapies in Hereditary Transthyretin Amyloidosis With Polyneuropathy: Real-World Insights From a German Single-Referral Center.

|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

|Mar 31, 2026

Effect of Eplontersen in Patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy Across Genetic Variants: An Exploratory Analysis From the NEURO-TTRansform Trial.

Julian D Gillmore, David Adams, Markus Weiler

|Jan 16, 2026

Choosing the optimal mouse model for the study of late-onset spinal muscular atrophy: Why the 4-copy <i>SMN2</i> model offers ideal translational relevance.

Markus Leo, Linda-Isabell Schmitt, Kai Christine Liebig

|Sep 12, 2025

Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study.

Benedikt Becker, Isabell Cordts, Jutta Becker

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Frequent Collaborators

Jennifer Kollmer

Ute Hegenbart

Wolfgang Wick

Stefan Schönland

Tobias Kessler

René Günther

Johann M E Jende

Georges Sam

Jana Müller

Selina Hein

Frequent Collaborators

Jennifer Kollmer

Ute Hegenbart

Wolfgang Wick

Stefan Schönland