Maike F Dohrn

26PUBLICATIONS
81CO-AUTHORS
Gene and molecular therapyNeurology and neuromuscular diseasesMedical infection agents (incl. prions)Sensory systemsMedical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (26)

|Aug 12, 2026
Disease modifying treatment of hereditary transthyretin amyloidosis with polyneuropathy in Germany - expert consensus of the German society of amyloid diseases (DGAK) and the German neurological society (DGN).

|Jun 24, 2026
Longitudinal five-year follow-up by muscle MRI and high-resolution nerve ultrasound in hereditary neuropathies.

|Feb 25, 2026
Mitofusin MFN2 acts as a molecular sensor preventing protein aggregation and mitophagy, with a protective effect against apoptosis in Charcot-Marie-Tooth type 2A disease.

Mariana Joaquim, Maike F Dohrn, Arnaud Chevrollier

|Oct 24, 2025
Altered NaV1.9 channel activity in two Tyr66Ser variant carriers with small fiber dysfunction.

Noortje W M van den Braak, Samuel Kuehs, Greta Z Peschke

|Jun 10, 2025
Disease spectrum and long-term prognosis of patients with BAG3-associated neuromuscular diseases in Europe.

Gorka Fernández-Eulate, Cyril Gitiaux, Simone Thiele

|Feb 12, 2025
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.

Andrea Cortese, Maike F Dohrn, Riccardo Curro

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Frequent Collaborators

6 joint publications

Stephan Zuchner

6 joint publications

Adriana Rebelo

5 joint publications

Danique Beijer

3 joint publications

Mary M Reilly