Publications and communications of Serpil ALKAN

Lumaka Zola, A., Fasquelle, C., Debray, F.-G., Alkan, S., Jacquinet, A., Harvengt, J., Boemer, F., Mulder, A., VAESSEN, S., Viellevoye, R., Gonon Rodrigues Palmeira, L., CHARLOTEAUX, B., Brysse, A., BULK, S., Rigo, V., & Bours, V. (16 February 2023). Rapid Whole Genome Sequencing Diagnoses and Guides Treatment in Critically Ill Children in Belgium in Less than 40 Hours. International Journal of Molecular Sciences, 24 (4), 4003. doi:10.3390/ijms24044003

DEPIERREUX, F., & ALKAN, S. (2022). Atypical Hemifacial Spasm and Myoclonus Related to AIFM1 Variant. Neuropediatrics. doi:10.1055/s-0042-1744159

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

HARVENGT, J., ALKAN, S., Florkin, B., BULK, S., & Bours, V. (June 2020). POP1-Skeletal dysplasias : description of two new families [Poster presentation]. European Human Genetics Virtual Conference 2020.

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.

ALKAN, S., DEMONCEAU, N., & LEWIN, M. (October 2018). L’image du mois: Atteinte isolée et retardée des ganglions de la base après intoxication à la méthadone. Revue Médicale de Liège, 73 (10), 485-487.

ALKAN, S., DEMONCEAU, N., & LEWIN, M. (October 2018). L'image du mois: Atteinte isolée et retardée des ganglions de la base après intoxication à la méthadone. Revue Médicale de Liège, 10 (73), 485-487.

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.

Alkan, S., Stouffs, K., Jansen, A., Misson, J.-P., Verloes, A., & JACQUINET, A. (16 February 2018). Circumferential skin creases and blepharophimosis are features associated with tubulinopathies : a case report and review of literature [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium.