Acute aortic dissection presenting as painless paraplegia: a case report

Por Hdiji, Olfa, Bouzidi, Nouha, Damak, Mariem, Mhiri, Chokri
Publicado no J Med Case Rep (2016)

Detection Methods of COVID-19

Por Echtioui, Amira, Zouch, Wassim, Ghorbel, Mohamed, Mhiri, Chokri, Hamam, Habib
Publicado no SLAS Technol (2020)

Myelopathy after zoster virus infection in immunocompetent patients: A case series

Por Farhat, Nouha, Daoud, Sawsan, Hdiji, Olfa, Sakka, Salma, Damak, Mariem, Mhiri, Chokri
Publicado no J Spinal Cord Med (2019)

Cerebral rheumatoid vasculitis: a case report

Por Akrout, Rim, Bendjemaa, Samar, Fourati, Hela, Ezzeddine, Mariem, Hachicha, Imène, Mhiri, Chokri, Baklouti, Soufiene
Publicado em 2012

Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy

Por Rekik, Imen, Boukhris, Amir, Ketata, Sourour, Amri, Mohamed, Essid, Nourhene, Feki, Imed, Mhiri, Chokri
Publicado em 2013

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation

Por Hdiji, Olfa, Turki, Emna, Bouzidi, Nouha, Bouchhima, Imen, Damak, Mariem, Bohlega, Saeed, Mhiri, Chokri
Publicado no J Mov Disord (2016)

Étalonnage du test des cinq mots dans une population tunisienne de sujets sains

Por Bouattour, Nadia, Farhat, Nouha, Hadjkacem, Hanen, Hdiji, Olfa, Sakka, Salma, Dammak, Mariem, Mhiri, Chokri
Publicado no Pan Afr Med J (2019)

Efficacy of botulinum toxin A for the treatment of hemiparesis in adults with chronic upper limb spasticity

Por Ghroubi, Sameh, Alila, Samar, Elleuch, Wafa, Ayed, Houda Ben, Mhiri, Chokri, Elleuch, Mohamed Habib
Publicado no Pan Afr Med J (2020)

Denoising and contrast-enhancement approach of magnetic resonance imaging glioblastoma brain tumors

Por Mzoughi, Hiba, Njeh, Ines, Ben Slima, Mohamed, Ben Hamida, Ahmed, Mhiri, Chokri, Ben Mahfoudh, Kheireddine
Publicado no J Med Imaging (Bellingham) (2019)

Smoldering multiple myeloma revealed by superior ophthalmic vein thrombosis

Por Bouattour, Nadia, Farhat, Nouha, Hamza, Nouha, Hadjkacem, Hanen, Hdiji, Olfa, Sakka, Salma, Dammak, Mariem, Mhiri, Chokri
Publicado no Saudi J Ophthalmol (2020)

Deep Multi-Scale 3D Convolutional Neural Network (CNN) for MRI Gliomas Brain Tumor Classification

Por Mzoughi, Hiba, Njeh, Ines, Wali, Ali, Slima, Mohamed Ben, BenHamida, Ahmed, Mhiri, Chokri, Mahfoudhe, Kharedine Ben
Publicado no J Digit Imaging (2020)

Rank-Two NMF Clustering for Glioblastoma Characterization

Por Bougacha, Aymen, Njeh, Ines, Boughariou, Jihene, Kammoun, Omar, Ben Mahfoudh, Kheireddine, Dammak, Mariem, Mhiri, Chokri, Ben Hamida, Ahmed
Publicado no J Healthc Eng (2018)

Prévalence de la fibrillation atriale non valvulaire et de l´accident vasculaire cérébral ischémique et facteurs associés à la fibrillation atriale non valvulaire chez les patients...

Por Bahloul, Amine, Bouattour, Nadia, Triki, Faten, Hammami, Rania, Charfeddine, Selma, Ellouze, Tarek, Mhiri, Chokri, Abid, Leila, Kammoun, Samir
Publicado no Pan Afr Med J (2021)

Facteurs pronostiques de mortalité par accident vasculaire cérébral artériel à la phase aiguë dans une population nord-africaine

Por Moalla, Khadija Sonda, Damak, Mariem, Chakroun, Olfa, Farhat, Nouha, Sakka, Salma, Hdiji, Olfa, Kacem, Hanen Haj, Rekik, Noureddine, Mhiri, Chokri
Publicado no Pan Afr Med J (2020)

Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort

Por Landoulsi, Zied, Benromdhan, Sawssan, Ben Djebara, Mouna, Damak, Mariem, Dallali, Hamza, Kefi, Rym, Abdelhak, Sonia, Gargouri-Berrechid, Amina, Mhiri, Chokri, Gouider, Riadh
Publicado no BMC Med Genet (2017)

Vertebral solitary bone plasmacytoma in a young adult with Trisomy 21: A case report

Por Bouattour, Nadia, Hdiji, Olfa, Hachicha, Anis, Kammoun, Brahim, Sakka, Salma, Farhat, Nouha, Hajkacem, Hanen, Kolsi, Fatma, Charfi, Slim, Dammak, Mariem, Boudawara, Zaher, Boudawara, Tahya, Mhiri, Chokri
Publicado no J Spinal Cord Med (2018)

A Prospective Multicenter Study for Assessing MusiQoL Validity among Arabic-Speaking MS Patients Treated with Subcutaneous Interferon β-1a

Por Al Jumah, Mohammed, Kojan, Suleiman, Alroughani, Raed, Cupler, Edward, Bohlega, Saeed, Daif, Abdulkader, Al Mujalli, Mousa, Al Harbi, Talal, El Tamawy, Mohamed, Ashour, Samia, Mhiri, Chokri, Gouider, Riadh, Jawhary, Ayah, El Boghdady, Ahmed, Hussein, Mohamed
Publicado no Mult Scler Int (2021)

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

Por Hanein, Sylvain, Martin, Elodie, Boukhris, Amir, Byrne, Paula, Goizet, Cyril, Hamri, Abdelmadjid, Benomar, Ali, Lossos, Alexander, Denora, Paola, Fernandez, José, Elleuch, Nizar, Forlani, Sylvie, Durr, Alexandra, Feki, Imed, Hutchinson, Michael, Santorelli, Filippo M., Mhiri, Chokri, Brice, Alexis, Stevanin, Giovanni
Publicado em 2008

Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

Por Martin, Elodie, Schüle, Rebecca, Smets, Katrien, Rastetter, Agnès, Boukhris, Amir, Loureiro, José L., Gonzalez, Michael A., Mundwiller, Emeline, Deconinck, Tine, Wessner, Marc, Jornea, Ludmila, Oteyza, Andrés Caballero, Durr, Alexandra, Martin, Jean-Jacques, Schöls, Ludger, Mhiri, Chokri, Lamari, Foudil, Züchner, Stephan, De Jonghe, Peter, Kabashi, Edor, Brice, Alexis, Stevanin, Giovanni
Publicado em 2013

Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia

Por Boukhris, Amir, Schule, Rebecca, Loureiro, José L., Lourenço, Charles Marques, Mundwiller, Emeline, Gonzalez, Michael A., Charles, Perrine, Gauthier, Julie, Rekik, Imen, Acosta Lebrigio, Rafael F., Gaussen, Marion, Speziani, Fiorella, Ferbert, Andreas, Feki, Imed, Caballero-Oteyza, Andrés, Dionne-Laporte, Alexandre, Amri, Mohamed, Noreau, Anne, Forlani, Sylvie, Cruz, Vitor T., Mochel, Fanny, Coutinho, Paula, Dion, Patrick, Mhiri, Chokri, Schols, Ludger, Pouget, Jean, Darios, Frédéric, Rouleau, Guy A., Marques, Wilson, Brice, Alexis, Durr, Alexandra, Zuchner, Stephan, Stevanin, Giovanni
Publicado em 2013