The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures von Pressler, Ronit M., Cilio, Maria Roberta, Mizrahi, Eli M., Moshé, Solomon L., Nunes, Magda L., Plouin, Perrine, Vanhatalo, Sampsa, Yozawitz, Elissa, de Vries, Linda S., Puthenveettil Vinayan, Kollencheri, Triki, Chahnez C., Wilmshurst, Jo M., Yamamoto, Hitoshi, Zuberi, Sameer M.

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Disruptions of neurological services, its causes and mitigation strategies during COVID-19: a global review von García-Azorín, David, Seeher, Katrin M., Newton, Charles R., Okubadejo, Njideka U., Pilotto, Andrea, Saylor, Deanna, Winkler, Andrea Sylvia, Charfi Triki, Chahnez, Leonardi, Matilde

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Complex genotypes in family with metachromatic leukodystrophy: Effect of trans and cis mutations distribution on the phenotype variability von Ben Issa, Abir, Kamoun, Fatma, Bouchaala, Wafa, Charfi Triki, Chahnez, Fakhfakh, Faiza

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Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy von Ben Said, Mariem, Jallouli, Olfa, Ben Aissa, Abir, Souissi, Amal, Kamoun, Fatma, Fakhfakh, Faiza, Masmoudi, Saber, Ben Ayed, Ikhlas, Charfi Triki, Chahnez

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Characterization of a missense variant in COG5 in a Tunisian patient with COG5-CDG syndrome and insights into the effect of non-synonymous variants on COG5 protein von Khabou, Boudour, Sahari, Umar Bin Mohamad, ben Issa, Abir, Bouchaala, Wafa, Szenker-Ravi, Emmanuelle, Yu Jin Ng, Alvin, Bonnard, Carine, Mbarek, Hamdi, Zeyaul, Islam, Fakhfakh, Faiza, Kammoun, Fatma, Reversade, Bruno, Charfi Triki, Chahnez

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Knowledge and attitudes toward epilepsy among people in Sfax region, Tunisia von Charfi Triki, Chahnez, Mguidich, Thouraya, Bouchaala, Wafa, Ben Ncir, Sihem, Chaari, Hayet, Fourati, Emna, Ketata, Sourour, Kallel, Raida, Kamoun, Fatma

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Case report: Compound heterozygous variants detected by next-generation sequencing in a Tunisian child with ataxia-telangiectasia von Ammous-Boukhris, Nihel, Abdelmaksoud-Dammak, Rania, Ben Ayed-Guerfali, Dorra, Guidara, Souhir, Jallouli, Olfa, Kamoun, Hassen, Charfi Triki, Chahnez, Mokdad-Gargouri, Raja

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First report of Tunisian patients with CDKL5‐related encephalopathy von Charfi Triki, Chahnez, Zouari Mallouli, Salma, Ben Jdila, Marwa, Ben Said, Mariem, Kamoun Feki, Fatma, Weckhuysen, Sarah, Masmoudi, Sabeur, Fakhfakh, Faiza

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What is a clinical practice guideline? A roadmap to their development. Special report from the Guidelines Task Force of the International League Against Epilepsy von Jetté, Nathalie, Kirkpatrick, Martin, Lin, Katia, Fernando, Sanjaya M. S., French, Jacqueline A., Jehi, Lara, Kumlien, Eva, Triki, Chahnez C., Wiebe, Samuel, Wilmshurst, Jo, Brigo, Francesco

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Global survey on disruption and mitigation of neurological services during COVID-19: the perspective of global international neurological patients and scientific associations von Triki, Chahnez Charfi, Leonardi, Matilde, Mallouli, Salma Zouari, Cacciatore, Martina, Karlshoej, Kimberly Coard, Magnani, Francesca Giulia, Newton, Charles R., Pilotto, Andrea, Saylor, Deanna, Westenberg, Erica, Walsh, Donna, Winkler, Andrea Sylvia, Thakur, Kiran T., Okubadejo, Njideka U., Garcia-Azorin, David

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A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature von Ben Issa, Abir, Ben Ayed, Ikhlas, Jallouli, Olfa, Souissi, Amal, Bouchaalla, Wafa, Ben Said, Mariem, Mallouli, Salma, Masmoudi, Saber, Charfi Triki, Chahnez, Hadj Kacem, Hassen, Kammoun, Fatma

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Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy von Jehi, Lara, Jette, Nathalie, Kwon, Churl‐Su, Josephson, Colin B., Burneo, Jorge G., Cendes, Fernando, Sperling, Michael R., Baxendale, Sallie, Busch, Robyn M., Triki, Chahnez Charfi, Cross, J. Helen, Ekstein, Dana, Englot, Dario J., Luan, Guoming, Palmini, Andre, Rios, Loreto, Wang, Xiongfei, Roessler, Karl, Rydenhag, Bertil, Ramantani, Georgia, Schuele, Stephan, Wilmshurst, Jo M., Wilson, Sarah, Wiebe, Samuel

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A large consanguineous family with a homozygous Metabotropic Glutamate Receptor 7 (mGlu7) variant and developmental epileptic encephalopathy: Effect on protein structure and ligand... von Jdila, Marwa Ben, Mignon-Ravix, Cécile, Ncir, Sihem Ben, Kammoun, Fatma, Fakhfakh, Faiza, Villard, Laurent, Triki, Chahnez

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Treatment of seizures in the neonate: Guidelines and consensus‐based recommendations—Special report from the ILAE Task Force on Neonatal Seizures von Pressler, Ronit M., Abend, Nicholas S., Auvin, Stéphan, Boylan, Geraldine, Brigo, Francesco, Cilio, Maria Roberta, De Vries, Linda S., Elia, Maurizio, Espeche, Alberto, Hahn, Cecil D., Inder, Terrie, Jette, Nathalie, Kakooza‐Mwesige, Angelina, Mader, Silke, Mizrahi, Eli M., Moshé, Solomon L., Nagarajan, Lakshmi, Noyman, Iris, Nunes, Magda L., Samia, Pauline, Shany, Eilon, Shellhaas, Renée A., Subota, Ann, Triki, Chahnez Charfi, Tsuchida, Tammy, Vinayan, Kollencheri Puthenveettil, Wilmshurst, Jo M., Yozawitz, Elissa G., Hartmann, Hans

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Fast processing and classification of epileptic seizures based on compressed EEG signals von Djemal, Achraf, Kallel, Ahmed Yahia, Ouni, Cherif, El Baccouch, Rihem, Bouchaala, Dhouha, Kammoun Feki, Fatma, Charfi Triki, Chahnez, Fakhfakh, Ahmed, Kanoun, Olfa

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Acute Demyelinating Syndromes: A report of child neurology department of Sfax University Hospital von Zouari Mallouli, Salma, Ben Nsir, Sihem, Bouchaala, Wafa, Kamoun Feki, Fatma, Charfi Triki, Chahnez

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Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene von Louhichi, Nacim, Bahloul, Emna, Marrakchi, Slaheddine, Othman, Houda Ben, Triki, Chahnez, Aloulou, Kawthar, Trabelsi, Lobna, Mahfouth, Nadia, Ayadi-Mnif, Zeineb, Keskes, Leila, Fakhfakh, Faiza, Turki, Hamida

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Lessons learned from COVID-19 impact of pandemic on children with neurological disorders in Sfax, Tunisia von Zouari Mallouli, Salma, Najjar, Sahar, Kamoun Feki, Fatma, Jallouli, Olfa, Ben Nsir, Sihem, Bouchaala, Wafa, Leonardi, Matilde, Charfi Triki, Chahnez

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Defining neonatal status epilepticus: A scoping review from the ILAE neonatal task force von Nunes, Magda L, Yozawitz, Elissa G, Wusthoff, Courtney J, Shellhaas, Renée A, Olivas-Peña, Efraín, Wilmshurst, Jo M, Pressler, Ronit M, Triki, Chahnez C, Hartmann, Hans, Inder, Terrie, Boylan, Geraldine B, Valente, Kette, Moshe, Solomon L, Mizrahi, Eli M, Abend, Nicholas S

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8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects von Ben Ayed, Ikhlas, Bouzid, Amal, Kammoun, Fatma, souissi, Amal, Jallouli, Olfa, Mallouli, Salma, Guidara, Souhir, Loukil, Salma, Aloulou, Hajer, Jbeli, Fida, Aouichaoui, Sahar, Abid, Dorra, Abdelhedi, Fatma, Triki, Chahnez, Kamoun, Hassen, Masmoudi, Saber

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