Vanden Brande, L., ALKAN, S., BARREA, C., & LEROY, P. (January 2022). Comment j’explore. Une macrocéphalie. Revue Médicale de Liège, 77 (1), 56-62. |
Barrea, C., JADOT, A., DEBRAY, F.-G., Vrancken, G., & Leroy, P. (2021). Comment j'explore... un trouble du spectre de l'autisme. Revue Médicale de Liège, 76 (10), 761-767. |
DEPIERREUX, F., PARMENTIER, E., HARDY, P.-Y., LEROY, P., & MAQUET, P. (January 2021). Successful treatment of hand dystonia with botulinum toxin in a DYT12 patient. Toxicon, 190S1 (January 2021), 16. |
BARREA, C., DEBRAY, F.-G., SIMON, M., & LEROY, P. (2020). Comment j’explore… Une pathologie organique à l’origine d’un trouble pédopsychiatrique. Revue Médicale de Liège, 75 (1). |
Steward, C. A., Roovers, J., Suner, M.-M., Gonzalez, J. M., Uszczynska-Ratajczak, B., Pervouchine, D., Fitzgerald, S., Viola, M., Stamberger, H., Hamdan, F. F., Ceulemans, B., LEROY, P., Nava, C., Lepine, A., Tapanari, E., Keiller, D., Abbs, S., Sanchis-Juan, A., Grozeva, D., ... Frankish, A. (02 December 2019). Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A. npj Genomic Medicine, 4, 31. doi:10.1038/s41525-019-0106-7 |
Ebetiuc, I., BULK, S., & LEROY, P. (2019). L'heterotopie nodulaire periventriculaire. Un cas pediatrique. Revue Médicale de Liège, 74 (7-8), 388-390. |
Geurten, C., FORGET, P., LEROY, P., HOYOUX, C., & BARREA, C. (2018). Methotrexate-induced Acute Myelopathy in a Teenager With High-risk Acute Lymphoblastic Leukemia. Journal of Pediatric Hematology/Oncology. |
BARREA, C., Nicolescu, C. R., & LEROY, P. (2018). Lafora disease and diabete - Enlarging clinical phenotype. Neuropediatrics. doi:10.1055/s-0038-1653932 |
BARREA, C., Nicolescu, C. R., & LEROY, P. (April 2018). Lafora disease and diabete - Enlarging clinical phenotype [Poster presentation]. Société Européenne de Neuropédiatrie. |
ALKAN, S., LEROY, P., & BULK, S. (16 February 2018). Confirmation of an association between CTNNB1 mutations and hyperekplexia [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. |
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