Utility of EEG on attention deficit–hyperactivity disorder (ADHD) von Mahmoud, Mariem Ben, Ali, Nadia Ben, Fray, Saloua, jamoussi, Hela, Chebbi, Slim, Fredj, Mohamed

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Gastrointestinal Dysfunction and Neuropathologic Correlations in Parkinson Disease von Mrabet, Saloua, Ben Ali, Nadia, Achouri, Afef, Dabbeche, Radhouene, Najjar, Taoufik, Haouet, Slim, Belal, Samir

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Cognitive impairment in multiple sclerosis: Utility of electroencephalography von Jamoussi, Hela, Ali, Nadia Ben, Missaoui, Yasmine, Cherif, Aroua, Oudia, Nouria, Anane, Nadya, Ftouhi, Lamia, Mahmoud, Mariem Ben, Fray, Saloua, Fredj, Mohamed

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Adult-onset Rasmussen encephalitis and Parry Romberg syndrome overlap von Jamoussi, Maha, Jamoussi, Hela, Fray, Saloua, Echebbi, Slim, Ben Ali, Nadia, Fredj, Mohamed

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Parkinsonism and Sjögren's Syndrome: A Fortuitous Association or a Shared Immunopathogenesis? von Belal, Samir, Achouri, Afef, Jalleli, Mohamed, Jamoussi, Hela, Fray, Saloua, Hmida, Intissar, Ben Ali, Nadia, Kchaou, Mariem, Echebbi, Slim

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Causality relationship between CO2 emissions, GDP and energy intensity in Tunisia von Ben Mbarek, Mounir, Ben Ali, Nadia, Feki, Rochdi

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Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease von Achouri-Rassas, Afef, Ali, Nadia Ben, Cherif, Aroua, Fray, Saloua, Siala, Hajer, Zakraoui, Nouria Oudiaa, Hadj-Fredj, Sondes, Kechaou, Mariem, Anane, Nadia, Echebi, Slim, Messaoud, Taieb, Belal, Samir

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Epileptic seizures and occupational exposure to solvents: a cases series von Mechergui, Najla, Youssef, Imen, Ben Charrada, Nejla, Ben Ali, Nadia, Fredj, Mohamed, Ladhari, Nizar

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Early psychiatrics symptoms in familial Alzheimer’s disease with presenilin 1 mutation (I83T) von Fray, Saloua, Ali, Nadia Ben, Rassas, Afef Achouri, Kechaou, Meriem, Oudiaa, Nouria, Cherif, Aroua, Echebbi, Slim, Messaoud, Taieb, Belal, Samir

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Improved design of advanced controller for a step up converter used in photovoltaic system von Ben Si Ali, Nadia, Benalia, Nadia, Zerzouri, Nora

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Identification of RS2234253 T96K polymorphism of TREM2 gene in Tunisian Alzheimer's disease population von Fray, Saloua, Achouri, Afef, Jamoussi, Hela, Mahmoud, Mariem Ben, Ali, Nadia Ben, Messaoud, Taieb, Fradj, Mohamed

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The presentation of headache in Neuro-Behçet's disease: Tunisian case-series von Mahbouli, Hela, Azzouz, Majdeddine, Jamoussi, Hela, Fray, Saloua, Mahmoud, Mariem Ben, Ali, Nadia Ben, Fradj, Mohamed

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Quality of sleep in stroke survivors: A cross-sectional study in a Tunisian cohort von Majoul, Mohamed Slim, Bouchendira, Mariem, Jamoussi, Hela, Ben Mahmoud, Mariem, Fray, Saloua, Ali, Nadia Ben, Fradj, Mohamed

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Knowledge and attitudes toward epilepsy among teachers in Tunisia von Sansa, Emna, Fray, Saloua, Jamoussi, Hela, Chebbi, Slim, Ben Mahmoud, Mariem, Ben Ali, Nadia, Fredj, Mohamed

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Paraneoplastic neurological syndromes: A tunisian case series von Jamoussi, Maha, Jamoussi, Hela, Mahmoud, Mariem Ben, Fray, Saloua, Ali, Nadia Ben, Fradj, Mohamed

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Role of vitamin D receptor polymorphism in multiple sclerosis disease course von Jamoussi, Maha, Alaya, Faten, Jamoussi, Hela, Baraket, Ghada, Achouri, Afef, Mahmoud, Mariem Ben, Fray, Saloua, Ali, Nadia Ben, Messaoud, Taieb, Hannachi, Amal, Fradj, Mohamed

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Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlations von Jamoussi, Maha, Alaya, Faten, Jamoussi, Hela, Baraket, Ghada, Achouri, Afef, Mahmoud, Mariem Ben, Fray, Saloua, Ben Ali, Nadia, Messaoud, Taieb, Hannachi Salhi, Amel, Fredj, Mohamed

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Daytime sleepiness in myotonic dystrophy type 1 in Tunisian population von Kacem, Emna, Sakka, Salma, Laaroussi, Syrine, Ali, Nadia Ben, Farhat, Nouha, Hdiji, Olfa, Hajkacem, Hanene, Daoud, Sawsan, Moalla, Khadija Sonda, Damak, Mariem, Mhiri, Chokri

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IL6 and IL17 as inflammatory response in a case of Neurobrucellosis presenting as Leucoencephalopathy (P5.117) von Kchaou, Mariem, Belguith, Mariem, Bahrini, khadija, jalleli, Mohamed, echebbi, slim, jamoussi, hela, ben ali, nadia, Fredj, Mohamed, barbouche, ridha

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TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy? von Daghsni, Marwa, Lahbib, Saida, Fradj, Mohamed, Sayeb, Marwa, Kelmemi, Wided, Kraoua, Lilia, Kchaou, Mariem, Maazoul, Faouzi, Echebbi, Slim, Ben Ali, Nadia, Abdelhak, Sonia, M'rad, Ridha

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