Leber optic hereditary neuropathy plus dystonia by Mahoui, S., Belkhamsa, O., Ait Kaci, I., Abada Bendib, M., Castelnovo, G.

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Atypical pantothenate kinase-associated neurodegeneration: Clinical description of two brothers and a review of the literature by Mahoui, S., Benhaddadi, A., Ameur El Khedoud, W., Abada Bendib, M., Chaouch, M.

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Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families by Cancel, Géraldine, Dürr, Alexandra, Didierjean, Olivier, Imbert, Georges, Bürk, Katrin, Lezin, Agnès, Belal, Samir, Benomar, Ali, Abada-Bendib, Myriem, Vial, Christophe, Guimarães, João, Chneiweiss, Hervé, Stevanin, Giovanni, Yvert, Gael, Abbas, Nacer, Saudou, Frédéric, Lebre, Anne-Sophie, Yahyaoui, Mohamed, Hentati, Fayçal, Vernant, Jean-Claude, Klockgether, Thomas, Mandel, Jean-Louis, Agid, Yves, Brice, Alexis

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P070 IL-17 and nitric oxide pathways are involved in inflammatory response during Alzheimer’s disease: A study in Algerian patients by Belkhelfa, M., Rafa, H., Medjeber, O., Behairi, N., Abada-Bendib, M., Makrelouf, M., Belarbi, S., Masmoudi, A.N., Tazir, M., Touil-Boukoffa, C.

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Molecular and Clinical Correlations in Autosomal Dominant Cerebellar Ataxia with Progressive Macular Dystrophy (SCA7) by David, Gilles, Dürr, Alexandra, Stevanin, Giovanni, Cancel, Géraldine, Abbas, Nacer, Benomar, Ali, Belal, Samir, Lebre, Anne-Sophie, Abada-Bendib, Myriem, Grid, Djamel, Holmberg, Monica, Yahyaoui, Mohamed, Hentati, Fayçal, Chkili, Taïeb, Agid, Yves, Brice, Alexis

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Femme conductrice symptomatique de la dystrophie musculaire de Duchenne : à propos d’une observation by Abdelbaki, T., Abdelhak, S., Abada-Bendib, M., Masmoudi, A.N., Chekiri, A., Baba Ahmed, R.

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Myasthénie et anomalies thymiques (Étude rétrospective de 22 cas) by Kharchi, S., Belkada, S., Laiche, A., Abada-Bendib, M., Abdannaceur, M.

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Un syndrome confusionnel révélant une neurosyphilis by Saib, L., Si Ahmed, H., Bouchachi, S., Chabour, M., Abada Bendib, M., Nacer Masmoudi, A.

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Syndrome de Wolfram : à propos d’une famille by Agchariou, S., Ghecham, S., Kalafate, N., Abada Bendib, M., Masmoudi, A.N.

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Hypertension intra crânienne aiguë compliquant une sarcoïdose by Hakem, D., Médaoud, S., Lafer, A., Abada-Bendib, M., Morsli, M., Kessaci, F., Berrah, A.

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AVC du péripartum : expérience d’un service de médecine interne by Hakem, D., Abada-Bendib, M., Boudjelida, A., Boucelma, M., Kessaci, F., Berrah, A.

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Troubles psychiatriques révélant des tuberculoses leptoméningées chez des patients immunocompétents : revue de 2 observations by Hakem, D., Haddad, T., Ouadahi, N., Abada-Bendib, M., Laraba, N., Bouzifi, S., Mansouri, B., Berrah, A., Amrane, A.

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M - 5 Syndrome d’Allgrove : revue de 3 familles by Djemai, M., Abada-Bendib, M., Masmoudi, A.-N., Azzôug, M., Chentli, M.

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O - 12 Les manifestations neuro-ophtalmologiques révélatrices de maladies de système by Hakem, D., Berrah, A., Boucelma, M., Bendib-Abada, M., Ouadahi, N., Tiar, M.

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Screening for Proteins with Polyglutamine Expansions in Autosomal Dominant Cerebellar Ataxias by Stevanin, Giovanni, Trottier, Yvon, Cancel, Géraldine, Dürr, Alexandra, David, Gilles, Didierjean, Olivier, Bürk, Katrin, Imbert, Georges, Saudou, Frederic, Abada-Bendib, Myriem, Gourfinkel-An, Isabelle, Benomar, Ali, Abbas, Nacer, Klockgether, Thomas, Grid, Djamel, Agid, Yves, Mandel, Jean-Louis, Brice, Alexis

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Syndrome d'Allgrove : revue de trois familles by Djemai, M., Bendib-Abada, M., Matti, M., Ahmed, N. Baba, Masmoudi, A.-N.

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Encéphalopthie gravidique : penser à un hyperemesis gravidarum by Hakem, D., Lafer, H., Bendib-Abada, M., Boucelma, M., Derbal, F.-Z., Médaoud, S., Ouadahi, N., Berrah, A.

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P255 - L’encephalopathie de hashimoto by Ali, L.A., Azzoug, S., Bouhedda, R., Meziani, N., Abada-Bendib, M., Masmoudi, A., Chentli, F.

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Etiologies des lésions démyélinisantes cérébrales non liées à une sclérose en plaque : expérience d'un service de médecine interne by Lafer, H., Hakem, D., Boucelma, M., Bessas, S., Abada-Bendib, M., Bensalah, D., Djemai, M., Chouikrat, N., Kessaci, F., Ouadahi, N., Mansouri, B., Berrah, A.

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Leber optic hereditary neuropathy plus dystonia by Mahoui, S, Belkhamsa, O, Ait Kaci, I, Abada Bendib, M, Castelnovo, G

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