Hanns Lochmüller

53PUBLICATIONS
408CO-AUTHORS
Medical biochemistry - amino acids and metabolitesNeurology and neuromuscular diseasesOptometryMolecular medicineMedical molecular engineering of nucleic acids and proteins
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Publications (53)

|Jul 28, 2026
Hexosamine Pathway Disruption by GFPT1 Loss Drives Coordinated Defects in Glycosylation, Autophagy, and Trafficking.

|Jul 20, 2026
Systematic reanalysis of next-generation sequencing data in 101 neuromuscular disorder families enhances diagnostic yield, reveals intronic variants, and identifies a novel disease gene.

|Jul 13, 2026
Muscle Strength, Balance, and Indoor Mobility in Oculopharyngeal Muscular Dystrophy: An Exploratory Canadian Multicenter Study.

|May 15, 2026
Vamorolone Safety, Pharmacokinetics, and Exploratory Efficacy in Duchenne Muscular Dystrophy: A Phase II, Nonrandomized, Multiple-Dose Study in 2-<4-Year-Old Boys.

|Mar 03, 2026
A muscular dystrophy associated with bi-allelic LEMD2 variants: Expanding the genotype of nuclear envelopathies.

Marc Pauper, Heike Kölbel, Iakowos Karakesisoglou

|Mar 03, 2026
Results of a phase II open-label, multiple-dose study of vamorolone (VBP15-006) in 7- to < 18-year-old boys with duchenne muscular dystrophy.

Hanns Lochmüller, Hernan Gonorazky, Elisa Nigro

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Frequent Collaborators

11 joint publications

Rita Horvath

10 joint publications

Kiran Polavarapu

8 joint publications

Rachel Thompson

7 joint publications

Sergi Beltran