Search Results - "MHIRI, C"

Genetics of recessive ataxia by Mhiri, C

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RELATIONSHIP BETWEEN ALEXITHYMIA AND PARKINSON’S DISEASE IN A TUNISIAN SAMPLE by Messedi, N, Fakhfakh, E, Kolsi, S, Chaari, I, Charfeddine, F, Aribi, L, Farhat, N, Mhiri, C, Aloulou, J

“…IntroductionSeveral psychiatric signs are part of non-motor signs of parkinson’s disease (PD), including alexithymia.ObjectivesThe objective of this study is…”
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Mobilization of retrotransposons in synthetic allotetraploid tobacco by Petit, M, Guidat, C, Daniel, J, Denis, E, Montoriol, E, Bui, Q.T, Lim, K.Y, Kovarik, A, Leitch, A.R, Grandbastien, M-A, Mhiri, C

“…Allopolyploidy is a major driving force in plant evolution and can induce rapid structural changes in the hybrid genome. As major components of plant genomes,…”
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ANXIETY AND DEPRESSION IN TUNISIAN PATIENTS WITH PARKINSON’S DISEASE by Kolsi, S., Fakhfakh, E., Messedi, N., Chaari, I., Charfeddine, F., Aribi, L., Farhat, N., Mhiri, C., Aloulou, J.

“…Introduction Anxiodepressive disorders in Parkinson’s disease (PD) are quite frequent and considered as non-motor signs of the disease. Few studies have…”
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The bidirectional relationship between epilepsy and depression by Belghuith, S., Daoud, S., Smaoui, N., Farhat, N., Sakka, S., Hdiji, O., Moalla, K.S., Damak, M., Bouali, M. Maalej, Mhiri, C.

“…Introduction The relationship between epilepsy and depression has been recognized for a long time. In fact, the presence of depression could worsen the disease…”
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Emotional outcomes in tunisian stroke survivors by Charfi, N., Elleuch, S., Smaoui, N., Bouali, M. Maalej, Zouari, L., Dammak, M., Mhiri, C., Thabet, J. Ben, Maalej, M.

“…Introduction Depression and anxiety are recognized as common psychiatric complications of stroke, yet little is known about their clinical correlates and their…”
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Gayet wernicke encephalopathy: Don’t miss this neuropsychiatric emergency by Laroussi, S., Moalla, K.S., Hdiji, O., Sakka, S., Daoud, S., Hadjkacem, H., Farhat, N., Mhiri, C.

“…Introduction Gayet Wernicke Encephalopathy (GWE) is a diagnostic and therapeutic neuropsychiatric emergency due to thiamin deficiency (vitamin B1). Objectives…”
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Antinuclear antibodies positivity is not rare during multiple sclerosis and is associated with relapsing status and IgG oligoclonal bands positivity by Mejdoub, S., Feki, S., Farhat, N., Dammak, M., Hachicha, H., Sakka, S., Ayedi, A., Ayedi, F., Mhiri, C., Masmoudi, H.

“…•The positivity of ANA, a classic marker of CTD, is not rare during MS.•ANA positivity in MS was not associated with clinical expression of any CTD.•ANA…”
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Stress activation and genomic impact of Tnt1 retrotransposons in Solanaceae by Grandbastien, M-A, Audeon, C, Bonnivard, E, Casacuberta, J M, Chalhoub, B, Costa, A-P P, Le, Q H, Melayah, D, Petit, M, Poncet, C, Tam, S M, Van Sluys, M-A, Mhiri, C

“…Tnt1 elements are a superfamily of LTR-retrotransposons distributed in the Solanaceae plant family and represent good model systems for studying regulatory and…”
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An unusual presentation of secondary central nervous system T cell lymphoma by Mguidich, T., Sakka, S., Saguem, I., Kardoun, N., Farhat, N., Damak, M., Mhiri, C.

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Ritumixab efficacy in Treatment-resistant CIDP with tremor in an Antineurofascin155 seropositive pediatric case by Laroussi, S., Sakka, S., Belghuith, S., Farhat, N., Hdiji, O., Daoud, S., Moalla, K., Devaux, J., Damak, M., Mhiri, C.

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An unusual case of acute myelopathy: Surfer's myelopathy in a teenage gymnast by Bouattour, N., Farhat, N., Sakka, S., Hdiji, O., Daoud, S., Moalla, K., Damak, M., Mhiri, C.

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Neuromyelitis optica spectrum disorders in South of Tunisia: A rare entity with low seroprevalence of anti-aquaporin 4 autoantibodies by Mejdoub, S., Feki, S., Dammak, M., Farhat, N., Hdiji, O., Boukthir, S., Hachicha, H., Mhiri, C., Masmoudi, H.

“…Screening for anti-aquaporin 4 (anti-AQP4) antibodies, a specific marker of neuromyelitis optica spectrum disorders (NMOSD), is part of the immunological…”
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Cinical and ENMG findings in patients with rare variants of Guillain Barré Syndrome by Zouari, S., Haj Kacem, H., Sakka, S., Damak, M., Mhiri, C.

“…Acute inflammatory demyelinating polyradiculoneuropathy (AIDP) is the most recognized form of Guillain Barré Syndrome (GBS), while others variants such as…”
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Developmental venous anomalies and seizures: Coincidence or causation? by Zouari, R., Sakka, S., Ketata, S., Farhat, N., Hdiji, O., Hajkacem, H., Dammak, M., Mhiri, C.

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Antiphospholipid syndrome and polymyositis: a rare multiple autoimmune syndrome by Gargouri, M.A, Damak, M, Bouzidi, N, Bouchhima, I, Turki, E, Mhiri, C

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Cerebrovascular diseases complicating Crohn’s disease by Moalla, K, Turki, E, Bouchhima, I, Bouzidi, N, Damak, M, Mhiri, C

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When celiac disease touches neurons: a report of four patients by Gargouri, M.A, Damak, M, Turki, E, Bouchhima, I, Bouzidi, N, Mhiri, C

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CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5 by Goizet, Cyril, Boukhris, Amir, Durr, Alexandra, Beetz, Christian, Truchetto, Jeremy, Tesson, Christelle, Tsaousidou, Maria, Forlani, Sylvie, Guyant-Maréchal, Lucie, Fontaine, Bertrand, Guimarães, João, Isidor, Bertrand, Chazouillères, Olivier, Wendum, Dominique, Grid, Djamel, Chevy, Françoise, Chinnery, Patrick F., Coutinho, Paula, Azulay, Jean-Philippe, Feki, Imed, Mochel, Fanny, Wolf, Claude, Mhiri, Chokri, Crosby, Andrew, Brice, Alexis, Stevanin, Giovanni

“…Thirty-four different loci for hereditary spastic paraplegias have been mapped, and 16 responsible genes have been identified. Autosomal recessive forms of…”
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Dyke Davidoff Masson syndrome a rare cause of schizoaffective disorder: A case report and review of the literature by Hamza, N, Hdiji, O, Haj Kacem, H, Farhat, N, Sakka, S, Dammak, M, Mhiri, C

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