| ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions SM Zuberi, E Wirrell, E Yozawitz, JM Wilmshurst, N Specchio, K Riney, ... Epilepsia 63 (6), 1349-1397, 2022 | 342 | 2022 |
| The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures RM Pressler, MR Cilio, EM Mizrahi, SL Moshé, ML Nunes, P Plouin, ... Epilepsia 62 (3), 615-628, 2021 | 262 | 2021 |
| AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 186 | 2019 |
| The effect of a motor skills training program in the improvement of practiced and non-practiced tasks performance in children with developmental coordination disorder (DCD) F Farhat, I Hsairi, H Baati, BCM Smits-Engelsman, K Masmoudi, ... Human movement science 46, 10-22, 2016 | 107 | 2016 |
| New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a … N Louhichi, C Triki, S Quijano-Roy, P Richard, S Makri, M Méziou, ... neurogenetics 5, 27-34, 2004 | 100 | 2004 |
| Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy L Jehi, N Jette, CS Kwon, CB Josephson, JG Burneo, F Cendes, ... Epilepsia 63 (10), 2491-2506, 2022 | 66 | 2022 |
| The effects of 8 weeks of motor skill training on cardiorespiratory fitness and endurance performance in children with developmental coordination disorder F Farhat, K Masmoudi, I Hsairi, BCM Smits-Engelsman, R Mchirgui, ... Applied Physiology, Nutrition, and Metabolism 40 (12), 1269-1278, 2015 | 43 | 2015 |
| Disruptions of neurological services, its causes and mitigation strategies during COVID-19: a global review D García-Azorín, KM Seeher, CR Newton, NU Okubadejo, A Pilotto, ... Journal of neurology 268 (11), 3947-3960, 2021 | 40 | 2021 |
| New mutation c.374C>T and a putative disease‐associated haplotype within SCN1B gene in Tunisian families with febrile seizures N Fendri‐Kriaa, F Kammoun, IH Salem, C Kifagi, E Mkaouar‐Rebai, ... European journal of neurology 18 (5), 695-702, 2011 | 40 | 2011 |
| Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4–KCNQ2 genes loci H Elghezal, H Hannachi, S Mougou, H Kammoun, C Triki, A Saad European journal of medical genetics 50 (6), 441-445, 2007 | 32 | 2007 |
| A convolutional gated recurrent neural network for epileptic seizure prediction A Affes, A Mdhaffar, C Triki, M Jmaiel, B Freisleben How AI Impacts Urban Living and Public Health: 17th International Conference …, 2019 | 29 | 2019 |
| MRI features in 17 patients with l2 hydroxyglutaric aciduria H Fourati, E Ellouze, M Ahmadi, D Chaari, F Kamoun, I Hsairi, C Triki, ... European journal of radiology open 3, 245-250, 2016 | 28 | 2016 |
| Genetic screening of two Tunisian families with generalized epilepsy with febrile seizures plus N Fendri‐Kriaa, F Kammoun, A Rebai, D Kolsi, I Hadj Salem, F Fakhfakh, ... European journal of neurology 16 (6), 697-704, 2009 | 28 | 2009 |
| Treatment of seizures in the neonate: Guidelines and consensus‐based recommendations—Special report from the ILAE Task Force on Neonatal Seizures RM Pressler, NS Abend, S Auvin, G Boylan, F Brigo, MR Cilio, ... Epilepsia 64 (10), 2550-2570, 2023 | 27 | 2023 |
| Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene E Mkaouar-Rebai, E Ellouze, I Chamkha, F Kammoun, C Triki, F Fakhfakh Journal of Child Neurology 26 (1), 12-20, 2011 | 27 | 2011 |
| Mutational analysis of the mitochondrial tRNALeu (UUR) gene in Tunisian patients with mitochondrial diseases E Mkaouar-Rebai, A Tlili, S Masmoudi, N Belguith, I Charfeddine, M Mnif, ... Biochemical and Biophysical Research Communications 355 (4), 1031-1037, 2007 | 26 | 2007 |
| Founder effect confirmation of c. 241A> G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria NK Jellouli, I Hadj Salem, E Ellouz, Z Kamoun, N Kaabachi, C Triki, ... Journal of human genetics 59 (4), 216-222, 2014 | 25 | 2014 |
| A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder E Mkaouar-Rebai, F Kammoun, I Chamkha, N Kammoun, I Hsairi, C Triki, ... Journal of child neurology 25 (6), 770-775, 2010 | 25 | 2010 |
| Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNATrp in patients with Leigh syndrome E Mkaouar-Rebai, I Chamkha, F Kammoun, T Kammoun, H Aloulou, ... Molecular Genetics and Metabolism 97 (3), 179-184, 2009 | 24 | 2009 |
| A Novel Mutation in FGD4/FRABIN Causes Charcot Marie Tooth Disease Type 4H in Patients from a Consanguineous Tunisian Family C Boubaker, I Hsairi‐Guidara, C Castro, I Ayadi, A Boyer, E Kerkeni, ... Annals of Human Genetics 77 (4), 336-343, 2013 | 23 | 2013 |
