Search Results - "Frih Ayed, M."

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  1. 1

    Age- and gender-specific effects on VDR gene polymorphisms and risk of the development of multiple sclerosis in Tunisians: a preliminary study by Ben-Selma, W., Ben-Fredj, N., Chebel, S., Frih-Ayed, M., Aouni, M., Boukadida, J.

    Published in International journal of immunogenetics (01-06-2015)
    “…Summary The vitamin D receptor (VDR) polymorphisms have been reported to be associated with multiple sclerosis (MS); however, evidence remains conflicting. In…”
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    Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family by Messaoud, O., Ben Rekaya, M., Kefi, R., Chebel, S., Boughammoura‐Bouatay, A., Bel Hadj Ali, H., Gouider‐Khouja, N., Zili, J., FrihAyed, M., Mokhtar, I., Abdelhak, S., Zghal, M.

    Published in British journal of dermatology (1951) (01-04-2010)
    “…Summary Xeroderma pigmentosum (XP) is a rare genodermatosis predisposing to skin cancers. The disease is classified into eight groups. Among them, XP group A…”
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    Peripheral blood markers of oxidative stress in Parkinson's disease by Younes-Mhenni, S, Frih-Ayed, M, Kerkeni, A, Bost, M, Chazot, G

    Published in European neurology (01-01-2007)
    “…Oxidative stress and generation of reactive oxygen species are believed to be implicated in Parkinson's disease (PD). Erythrocyte activity of superoxide…”
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    Syndrome de Guillain Barré et atteinte du système nerveux central : rapport de deux cas by Nagazi, M., Aissi, M., Daoussi, N., Frih Ayed, M.

    Published in Neurophysiologie clinique (01-09-2019)
    “…Bien que le syndrome de Guillain-Barré (SGB) soit généralement considéré comme une neuropathie périphérique, il existe une possibilité d’atteinte centrale…”
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  7. 7

    Crises focales cognitives symptomatiques d’un cavernome temporal droit by Haddad, S., Nagazi, M., Brahmi, L., Aissi, M., Frih Ayed, M.

    Published in Neurophysiologie clinique (01-09-2019)
    “…L’épilepsie est une maladie chronique qui affecte 1 % de la population générale. Les crises focales cognitives avec idées forcées (CFCIF) sont rares. Elles…”
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  8. 8

    Biballism due to non-ketotic hyperglycaemia by Boughammoura-Bouatay, A, Chebel, S, Younes-Mhenni, S, Frih-Ayed, M

    Published in Diabetes & metabolism (01-12-2008)
    “…Abstract We describe the case of a 70-year-old woman, with type 1 diabetes mellitus, who suddenly developed a movement disorder on the left side of her body…”
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    Hypothyroïdie et manifestation neurologique inhabituelle : quelle relation ? by Aissi, M, Machraoui, R, Sayadi, H, Frih Ayed, M

    Published in Annales d'endocrinologie (01-10-2014)
    “…Introduction Le diagnostic de l’hypothyroïdie se fait habituellement sur l’association de manifestations somatiques, le plus souvent au premier plan et de…”
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  10. 10

    La maladie de Fahr: a propos de 4 observations by Aissi, M, Machraoui, R, Younes, S, Frih Ayed, M

    Published in Annales d'endocrinologie (01-10-2014)
    “…Introduction La maladie de de Fahr défini par des calcifications striato-pallido-dentelées, non artériosclérotiques, est une entité rare caractérisée par son…”
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    Surpoids et obésité : facteurs de risque de la sclérose en plaques by Mahmoud, I., Dr, Aissi, M., Dr, Younes, S., Dr, Frih Ayed, M., Dr

    Published in Annales d'endocrinologie (01-09-2015)
    “…Introduction En plus d’être associée au diabète et aux maladies cardiaques, l’obésité pourrait aussi être liée à des maladies auto-immunes comme la sclérose en…”
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    Tuberous sclerosis and intracranial aneurysms: a rare association by Aissi, M, Younes-Mhenni, S, Jerbi-Ommezzine, S, Boughammoura-Bouatay, A, Frih-Ayed, M, Sfar, M H

    Published in Revue neurologique (01-11-2010)
    “…Tuberous sclerosis is an autosomal dominant inherited phakomatosis. It is associated with a wide variety of central nervous system abnormalities, but…”
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    Multiple cranial nerve involvement: consider the diagnosis of cephalic tetanus. A case report and review of the literature by Chebel, S, Letaief, L, Boughammoura-Bouatay, A, Dachraoui, F, Ouanes, I, Ouanes-Besbes, L, Abroug, F, Frih-Ayed, M

    Published in Revue neurologique (01-11-2010)
    “…Cephalic tetanus is the most serious form of localized tetanus. It associates trismus with impairment of one or more cranial nerves. It was a rare condition,…”
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    Crises épileptiques et hyperglycémie sans cétose étude de série by Aissi, M, Rekik, M, Machraoui, R, Younes, S, Sayadi, H, Frih Ayed, M

    Published in Annales d'endocrinologie (01-10-2014)
    “…Introduction Depuis le premier cas décrit en 1965, les cas de crises d’épilepsie secondaire à une hyperglycémie sans cétose sont de plus en plus fréquents,…”
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    Pseudotumoral presentation of multiple sclerosis by Chebel, S, Rekik, O, Boughammoura-Bouatay, A, Frih-Ayed, M

    Published in Neuro-chirurgie (01-11-2007)
    “…Multiple sclerosis is one of the most common diseases of the central nervous system with a variety of clinical and radiological presentations. Several cases…”
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    Lobstein's disease presenting with seizures by Boughammoura-Bouatay, A, Chebel, S, Aissi, M, Koubaa, M, Frih-Ayed, M

    Published in Revue neurologique (01-09-2007)
    “…Osteogenesis imperfecta (OI) is a group of hereditary disorders most often due to an anomaly of collagen biosynthesis. Divers clinical manifestations are…”
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    A clinical and magnetic resonance spectroscopy study of a brain tumor in a patient with segmental neurofibromatosis by Chebel, S, Yahia, S. Ben, Boughammoura-Bouatay, A, Salem, R, Golli, M, Khairallah, M, Frih-Ayed, M

    Published in Neuro-chirurgie (01-08-2010)
    “…Abstract Introduction Segmental neurofibromatosis 1 (segmental NF-1) is a rare genodermatosis caused by somatic mutations in the NF-1 gene. It consists of…”
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    Coeliac disease an spastic paraplegia by Frih-Ayed, M, Boughammoura-Bouatay, A, Fitouri, F, Chebel, S

    Published in Revue neurologique (01-05-2006)
    “…Celiac disease (CD) is an immune-mediated disease triggered by the ingestion of gluten in genetically susceptible individuals. Neurological manifestations are…”
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    Épilepsie temporale symptomatique d’une méningocèle intracrânienne chez une patiente atteinte de neurofibromatose de type 1 by Boughammoura, A, Daoussi, N, Younes, S, Kilani, M, Chebel, S, Hattab, M, Frih-Ayed, M

    Published in Neuro-chirurgie (01-08-2013)
    “…Abstract Epilepsy has been rarely reported in patients with neurofibromatosis type 1 (formally known as von Recklinghausen disease), which may occur in 3 to 6%…”
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