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Dellatte Julien

Dép. des Sciences de l'activité phys. et de la réadaptation

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Main Referenced Co-authors
Wang, François  (5)
Lievens, Isabelle  (4)
Kaux, Jean-François  (3)
Tyberghein, Maelle  (2)
Bruyère, Olivier  (1)
Main Referenced Keywords
Femoroacetabular impingement (1); General Medicine (1); MME gene (1); Neurology (clinical) (1); Orthopedics and Sports Medicine (1);
Main Referenced Disciplines
Neurology (5)
Laboratory medicine & medical technology (1)
Orthopedics, rehabilitation & sports medicine (1)

Publications (total 7)

The most downloaded
311 downloads
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). https://hdl.handle.net/2268/226662

Leroy, R., Thirion, T., Kaux, J.-F., Dunand, X., Croisier, J.-L., Dellatte, J., & Delvaux, F. (13 September 2025). Conflits fémoro-acétabulaires, options de traitement et rééducation: une revue narrative (partie 2). Journal de Traumatologie du Sport, 42 (3), 234-240. doi:10.1016/j.jts.2024.01.004
Peer Reviewed verified by ORBi

HUSTINX, M., Dellatte, J., LIEVENS, I., Tyberghein, M., & Wang, F. (June 2023). N°119 – Different nerve excitability measurements in a rare case of CMT1H. Clinical Neurophysiology, 150, 110. doi:10.1016/j.clinph.2023.03.122
Peer Reviewed verified by ORBi

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.
Peer reviewed

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
Peer Reviewed verified by ORBi

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.
Peer reviewed

Dellatte, J., Leclercq, V., Kaux, J.-F., Bruyère, O., & Martens, G. (November 2021). Self-medication in fitness centers. British Journal of Sports Medicine, 55 (S1), 135-136. doi:10.1136/bjsports-2021-IOC.325
Peer Reviewed verified by ORBi

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).
Peer reviewed

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