May home cardiorespiratory polygraphy be considered a realistic alternative to polysomnography for catathrenia screening? von Msaad, Sameh, Abid, Sourour, Wadhane, Issraa, Gargouri, Rahma, Kallel, Nesrine, Triki, Fatma, Moussa, Nadia, Kammoun, Samy

Volltext

Impact de l’audit externe sur la qualité du résultat comptable : cas des entreprises tunisiennes cotées von Omri, Abdelwahed, Ghorbel, Faten Hakim, Baklouti, Fatma Triki

Volltext

Narcolepsy von Msaad, Sameh, Ayadi, Hajer, Triki, Fatma, Kawas, Hamida, Yangui, Ilhem, Ayoub, Abdelkader

Volltext

La narcolepsie von MSAAD, Sameh, AYADI, Hajer, TRIKI, Fatma, KAWAS, Hamida, YANGUI, Ilhem, AYOUB, Abdelkader

Volltext

Development of an in-house quantitative ELISA for the evaluation of different Covid-19 vaccines in humans von Gdoura, Mariem, Ghaloum, Fatma Ben, Hamida, Meriem Ben, Chamsa, Wafa, Triki, Henda, Bahloul, Chokri

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Elevated Interleukin-21 expression is correlated with systemic sclerosis’ severity in Tunisian patients von Dlala, Akram, Gabsi, Amira, Ben Salem, Khalil, Boutabba, Alya, Nacer, Ines, Missaoui, Fadoua, Neili, Bilel, Saïd, Fatma, Smiti-Khanfir, Monia, Triki-Marrakchi, Raja

Volltext

First description of novel compound heterozygous mutations in HYCC1: clinical evaluations and molecular analysis in patient with hypomyelinating leukodystrophy-5 with retrospective... von Ben Issa, Abir, Kamoun, Fatma, Khabou, Boudour, Bouchaala, Wafa, Fakhfakh, Faiza, Triki, Chahnez

Volltext

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

Volltext

Molecular Epidemiology of SARS-CoV-2 in Tunisia (North Africa) through Several Successive Waves of COVID-19 von Chouikha, Anissa, Fares, Wasfi, Laamari, Asma, Haddad-Boubaker, Sondes, Belaiba, Zeineb, Ghedira, Kais, Kammoun Rebai, Wafa, Ayouni, Kaouther, Khedhiri, Marwa, Ben Halima, Samar, Krichen, Henda, Touzi, Henda, Ben Dhifallah, Imen, Guerfali, Fatma Z, Atri, Chiraz, Azouz, Saifeddine, Khamessi, Oussema, Ardhaoui, Monia, Safer, Mouna, Ben Alaya, Nissaf, Guizani, Ikram, Kefi, Rym, Gdoura, Mariem, Triki, Henda

Volltext

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

Volltext

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

Volltext

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

Volltext

Mitochondrial leucoencephalopathies: An under-diagnosed form of mitochondrial disease von Zouari, Rania, Triki, Chahnez, Bouchaala, Wafa, Nsir, Sihem Ben, Kamoun, Fatma

Volltext

Peripheral neuropathy due to mitochondrial disorders in pediatric patients von Zouari, Rania, Triki, Chahnez, Bouchaala, Wafa, Nsir, Sihem Ben, Kamoun, Fatma

Volltext

Synergistic effect of polysaccharides, betalain pigment and phenolic compounds of red prickly pear (Opuntia stricta) in the stabilization of salami von Kharrat, Nadia, Salem, Hedia, Mrabet, Aicha, Aloui, Fatma, Triki, Soumaya, Fendri, Ahmed, Gargouri, Youssef

Volltext

Mutation in the β-tubulin gene TUBB4A results in epileptic encephalopathy associated with hypomyelinated leucodystrophy: Unexpected findings reveal genetic mosaicism von Ben Jdila, Marwa, Kammoun, Fatma, Abdelmaksoud-Dammak, Rania, Triki, Chahnez, Fakhfakh, Faiza

Volltext