John Rendu

15PUBLICATIONS
94CO-AUTHORS
Neurology and neuromuscular diseasesMechanobiologyMedical devicesCancer geneticsInfant and child health
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Publications (15)

|Aug 18, 2026
Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

|Jun 08, 2026
Reducing Body Myopathy in Female Patients With FHL1 Variants Showing Rapid and Severe Evolution Mimicking Inflammatory Myopathy: A Case Series.

|May 13, 2026
Drosophila ryanodine receptor gene triggers functional and developmental muscle properties and could be used to assess the impact of human RYR1 mutations.

|Feb 26, 2026
Histogenetic Classification Predicts Outcomes in 130 Adults With Chronic Intestinal Pseudo-Obstruction.

Minh-Chau Ta, Dominique Cazals-Hatem, Lore Billiauws

|Feb 09, 2023
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders.

Afshin Saffari, Tracy Lau, Homa Tajsharghi

|Dec 08, 2021
Diagnostic workup in children with arthrogryposis: description of practices from a single reference centre, comparison with literature and suggestion of recommendations.

Pauline Le Tanno, Xenia Latypova, John Rendu

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Frequent Collaborators

3 joint publications

Mireille Cossée

3 joint publications

Norma Beatriz Romero

2 joint publications

Klaus Dieterich

2 joint publications

Jorge Alfredo Bevilacqua