Publications and communications of Patricia LEROY

Tretjakova, M., Leroy, P., & Barrea, C. (10 July 2023). Acute encephalopathy in a neonate associated with infection by SARS-CoV-2. Belgian Journal of Paediatrics, 25 (2), 184-186.

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).

BARREA, C., LEROY, P., DEBRAY, F.-G., ALKAN, S., & Rousselle, L. (2020). Comment j’explore… Un trouble du développement intellectuel chez l'enfant. Revue Médicale de Liège, 75 (10), 686-691.

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

Fazzi, E., Korff, C. M., Bernabe Gelot, A., LEROY, P., Rivier, F., San Antonio-Arce, V., & Veggiotti, P. (November 2019). Neurodevelopmental problems of unaccompanied refugee and migrant children: a new challenge for pediatric neurologists [letter to the editor]. Developmental Medicine and Child Neurology, 61 (11), 1348. doi:10.1111/dmcn.14275

DEPIERREUX, F., PARMENTIER, E., HARDY, P.-Y., LEROY, P., & MAQUET, P. (11 May 2019). Successful treatment of hand dystonia with Botulinum Toxin in a DYT12 patient [Poster presentation]. Fourth International Congress on Treatment of Dystonia, Hanovre, Germany.

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.

LEROY, P., Meyer, F., Vaessen, S., Doummar, D., & Misson, J.-P. (July 2017). Dystonie de type 12 : un diagnostic rare et difficile. Archives de Pédiatrie, 24 (7), 637-639. doi:10.1016/j.arcped.2017.04.010

Vaessen, S., DARON, A., DUBRU, J.-M., Ebetiuc, I., Leroy, P., & Misson, J.-P. (2012). Aspects neurologiques associés au Syndrome de Down. Tijdschrift van de Belgische Kinderarts, 14 (2), 40-43.