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Leroy Patricia

Département des sciences cliniques

See author's contact details
Main Referenced Co-authors
Barrea, Christophe  (9)
Debray, François-Guillaume  (5)
Alkan, Serpil  (4)
Bulk, Saskia  (4)
Bours, Vincent  (2)
Main Referenced Keywords
Humans (4); Male (3); Botulinum toxin (2); Child (2); Female (2);
Main Referenced Unit & Research Centers
GIGA CRC (Cyclotron Research Center) In vivo Imaging-Aging & Memory - ULiège (1)
Main Referenced Disciplines
Pediatrics (12)
Neurology (9)
Genetics & genetic processes (4)
General & internal medicine (1)

Publications (total 19)

The most downloaded
4283 downloads
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. https://hdl.handle.net/2268/129552

The most cited

39 citations (OpenAlex)

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 https://hdl.handle.net/2268/244273

Boemer, F., Hovhannesyan, K., Piazzon, F., MINNER, F., Mni, M., Jacquemin, V., Mashhadizadeh, D., BENMHAMMED, N., Bours, V., Jacquinet, A., Harvengt, J., Bulk, S., Dideberg, V., Helou, L., Palmeira, L., Dangouloff, T., BabyDetect Expert Panel, Servais, L., Alkan, S. (Other coll.), ... Vaessen, S. (Other coll.). (28 January 2025). Population-based, first-tier genomic newborn screening in the maternity ward. Nature Medicine, 31 (4), 1339-1350. doi:10.1038/s41591-024-03465-x
Peer Reviewed verified by ORBi

Beckers, M., Stevens, R., Debray, F.-G., & Leroy, P. (July 2024). Impact neurodéveloppemental d’une mutation sur le gène RHOBTB2. Revue Médicale de Liège, 79 (7-8), 467-470.
Editorial Reviewed verified by ORBi

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.
Peer Reviewed verified by ORBi

Chatelain, C., Harvengt, J., Leroy, P. (Other coll.), CABERG, J.-H. (Other coll.), Debray, F.-G. (Other coll.), BULK, S. (Other coll.), & Bours, V. (Other coll.). (17 March 2023). Missense variant c.593A>G p.(Lys198Arg) in CSNK2A1, a recurrent variant in Okur-Chung neurodevelopmental syndrome: a case report and review of literature [Poster presentation]. Annual Meeting : To DNA and beyond, Charleroi, Belgium.

Vanden Brande, L., ALKAN, S., BARREA, C., & LEROY, P. (January 2022). Comment j’explore. Une macrocéphalie. Revue Médicale de Liège, 77 (1), 56-62.
Peer reviewed

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.
Peer Reviewed verified by ORBi

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.
Peer reviewed

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.
Peer reviewed

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).
Peer reviewed

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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.
Peer Reviewed verified by ORBi

BARREA, C., Nicolescu, C. R., & LEROY, P. (2018). Lafora disease and diabete - Enlarging clinical phenotype. Neuropediatrics. doi:10.1055/s-0038-1653932
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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.
Peer reviewed

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