Cerebrospinal fluid IL-10 as an early stage discriminative marker between multiple sclerosis and neuro-Behçet disease
Belghith, Meriam, Bahrini, Khadija, Kchaou, Mariem, Maghrebi, Olfa, Belal, Samir, Barbouche, Mohamed Ridha
Published in Cytokine (Philadelphia, Pa.) (01.08.2018)
Published in Cytokine (Philadelphia, Pa.) (01.08.2018)
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Neuromyelitis optica and concomitant pulmonary tuberculosis: a case report
Saied, Zakaria, Nabli, Fatma, Rachdi, Amine, Jeridi, Cyrine, Douma, Bissene, Belal, Samir, Ben Sassi, Samia
Published in Journal of medical case reports (06.08.2021)
Published in Journal of medical case reports (06.08.2021)
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Differential Gene Expression Patterns in Blood and Cerebrospinal Fluid of Multiple Sclerosis and Neuro-Behçet Disease
Maghrebi, Olfa, Hanachi, Mariem, Bahrini, Khadija, Kchaou, Mariem, Jeridi, Cyrine, Belal, Samir, Ben Sassi, Samia, Barbouche, Mohamed-Ridha, Souiai, Oussama, Belghith, Meriam
Published in Frontiers in genetics (26.02.2021)
Published in Frontiers in genetics (26.02.2021)
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Increased T-bet/GATA-3 and ROR-γt /Foxp3 Ratios in Cerebrospinal Fluid as Potential Criteria for Definite Neuro-Behçet’s Disease
Belghith, Meriam, Maghrebi, Olfa, Cherif, Aroua, Bahrini, Khadija, Saied, Zakaria, Belal, Samir, Sassi, Samia Ben, Barbouche, Mohamed-Ridha, Kchaou, Mariem
Published in Journal of clinical medicine (29.07.2022)
Published in Journal of clinical medicine (29.07.2022)
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The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
Koenig, Michel, Belal, Samir, Hentati, Fayçal, Bomont, Pascale, Cavalier, Laurent, Demir, Ercan, Korinthenberg, Rudolf, Tüysüz, Beyhan, Hamida, Christiane Ben, Blondeau, François, Topaloglu, Haluk, Landrieu, Pierre, Tazir, Meriem
Published in Nature genetics (01.11.2000)
Published in Nature genetics (01.11.2000)
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Parkinsonism and Sjögren's Syndrome: A Fortuitous Association or a Shared Immunopathogenesis?
Belal, Samir, Achouri, Afef, Jalleli, Mohamed, Jamoussi, Hela, Fray, Saloua, Hmida, Intissar, Ben Ali, Nadia, Kchaou, Mariem, Echebbi, Slim
Published in Case Reports in Medicine (01.01.2015)
Published in Case Reports in Medicine (01.01.2015)
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Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
Gouider-Khouja, Neziha, Larnaout, Abdelmajid, Amouri, Rim, Sfar, Sana, Belal, Samir, Ben Hamida, Christiane, Ben Hamida, Mongi, Hattori, Nobutaka, Mizuno, Yoshikuni, Hentati, Fayçal
Published in Parkinsonism & related disorders (01.06.2003)
Published in Parkinsonism & related disorders (01.06.2003)
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Missing apolipoprotein E ɛ4 allele associated with nonamnestic Alzheimer’s disease in a Tunisian population
Fray, Saloua, Achouri-Rassas, Afef, Belal, Samir, Messaoud, Taieb
Published in Journal of genetics (06.09.2022)
Published in Journal of genetics (06.09.2022)
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Atypical anti-NMDA receptor encephalitis associated with varicella zoster virus infection
Fatma, Nabli, Zakaria, Saied, Mourad, Zouari, Samir, Belal, Samia, Ben Sassi
Published in Journal of neurovirology (01.06.2022)
Published in Journal of neurovirology (01.06.2022)
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Association between H2 haplotype of microtubule associated protein tau gene (deletion / insertion) with Alzheimer Disease in Tunisian patients
Fray, Saloua, Achouri-Rassas, Afef Achouri, Hadj Fredj, Sondes, Messaoud, Taieb, Belal, Samir
Published in Neurological research (New York) (02.09.2022)
Published in Neurological research (New York) (02.09.2022)
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Journal Article
Myasthenia gravis and COVID‐19: A case series and comparison with literature
Saied, Zakaria, Rachdi, Amine, Thamlaoui, Saber, Nabli, Fatma, Jeridi, Cyrine, Baffoun, Nader, Kaddour, Chokri, Belal, Samir, Ben Sassi, Samia
Published in Acta Neurologica Scandinavica (01.09.2021)
Published in Acta Neurologica Scandinavica (01.09.2021)
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Increased IL-22 in cerebrospinal fluid of neuro-behçet’s disease patients
Belghith, Meriam, Maghrebi, Olfa, Ben Laamari, Rafika, Hanachi, Mariem, Hrir, Sana, Saied, Zakaria, Belal, Samir, Driss, Adel, Ben Sassi, Samia, Boussoffara, Thouraya, Barbouche, Mohamed-Ridha
Published in Cytokine (Philadelphia, Pa.) (01.07.2024)
Published in Cytokine (Philadelphia, Pa.) (01.07.2024)
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Impacts of Iron Metabolism Dysregulation on Alzheimer's Disease
Jouini, Najla, Saied, Zakaria, Ben Sassi, Samia, Nebli, Fatma, Messaoud, Taieb, Hentati, Faycel, Belal, Samir
Published in Journal of Alzheimer's disease (01.01.2021)
Published in Journal of Alzheimer's disease (01.01.2021)
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Missing apolipoprotein E ε4 allele associated with nonamnestic Alzheimer's disease in a Tunisian population
Fray, Saloua, Achouri-Rassas, Afef, Belal, Samir, Messaoud, Taieb
Published in Journal of genetics (01.01.2022)
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Published in Journal of genetics (01.01.2022)
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Discriminative expression of CD39 and CD73 in Cerebrospinal fluid of patients with Multiple Sclerosis and Neuro-Behçet’s disease
Bahrini, Khadija, Belghith, Meriam, Maghrebi, Olfa, Bekir, Jihène, Kchaou, Mariem, Jeridi, Cyrine, Amouri, Rim, Hentati, Faycel, Belal, Samir, Ben Sassi, Samia, Barbouche, Mohamed-Ridha
Published in Cytokine (Philadelphia, Pa.) (01.06.2020)
Published in Cytokine (Philadelphia, Pa.) (01.06.2020)
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Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping
Nicole, S, Ben Hamida, C, Beighton, P, Bakouri, S, Belal, S, Romero, N, Viljoen, D, Ponsot, G, Sammoud, A, Weissenbach, J
Published in Human molecular genetics (01.09.1995)
Published in Human molecular genetics (01.09.1995)
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Extending brainstem and capsule-thalamic lesions in a patient with parenchymal neuro-Behçet disease
Saied, Zakaria, Cyrine, Jeridi, Fatma, Nabli, Medini, Myriam, Samir, Belal, Ben Sassi, Samia
Published in Imaging (Budapest) (23.12.2022)
Published in Imaging (Budapest) (23.12.2022)
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Journal Article
Ataxia with vitamin E deficiency : refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families
DOERFLINGER, N, LINDER, C, MONGI BEN HAMIDA, PANDOLFO, M, DIDONATO, S, SOKOL, R, KAYDEN, H, LANDRIEU, P, DURR, A, BRICE, A, GOUTIERES, F, KOHLSCHÜTTER, A, OUAHCHI, K, SABOURAUD, P, ALI BENOMAR, MOHAMED YAHYAOUI, MANDEL, J.-L, KOENIG, M, GYAPAY, G, WEISSENBACH, J, LE PASLIER, D, RIGAULT, P, SAMIR BELAL, BEN HAMIDA, C, HENTATI, F
Published in American journal of human genetics (01.05.1995)
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Published in American journal of human genetics (01.05.1995)
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