Publications and communications of Julien Dellatte

Hustinx, M., Dellatte, J., Lievens, I., Tyberghein, M., & Wang, F.-C. (May 2023). Different nerve excitability measurements in a rare case of CMT1H [Poster presentation]. ECCN 2023, Marseille, France.

Dellatte, J., Lievens, I., & Wang, F.-C. (2023). Could some mutations of the KIF5A gene be responsible for a dominant CMT2 phenotype? (Case report). Acta Neurologica Belgica. doi:10.1007/s13760-023-02248-4

Dellatte, J., LIEVENS, I., & WANG, F.-C. (May 2022). Une rare mutation du gène KIF5A associée à un tableau de CMT2 sans signe de spasticité : cas clinique [Poster presentation]. 22èmes Journées Francophones d'ElectroNeuroMyoGraphie, Marrakech, Morocco.

COLLIN, R., Dellatte, J., WANG, F.-C., & KAUX, J.-F. (2018). MME GENE MUTATION CAUSING SPINOCEREBELLAR ATAXIA AND AXONAL POLYNEUROPATHY: CLINICAL CASE. In 21st European Congress of Physical and Rehabilitation Medicine (pp. 223).