John Rendu

14PUBLICATIONS

78CO-AUTHORS

MechanobiologyMedical devicesCancer geneticsNeurology and neuromuscular diseasesInfant and child health

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Publications (14)

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|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

|Feb 09, 2022

Congenital Nemaline Myopathy with Dense Protein Masses.

Jorge A Bevilacqua, Edoardo Malfatti, Clémence Labasse

|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

Mireille Cossée

Klaus Dieterich

Norma Beatriz Romero

Whalen Sandra

Rocío N Villar-Quiles

Alan H Beggs

Anne-Cécile Coville

Dominique Lasne

François-Jérôme Authier

1 joint publications

Dominique Pidard

Frequent Collaborators

Mireille Cossée

Klaus Dieterich

Norma Beatriz Romero

Whalen Sandra