Search Results - "Boukhris, A"

Numerical study of heat and mass transfer in a desalination system by El Baamrani, H., Bammou, L., Aharoune, A., Boukhris, A.

“…In today’s world the demand for freshwater, to meet the needs of human activities is growing exponentially. As a result, manufacturers are continuing to make…”
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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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SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum by Goizet, C, Boukhris, A, Maltete, D, Guyant-Maréchal, L, Truchetto, J, Mundwiller, E, Hanein, S, Jonveaux, P, Roelens, F, Loureiro, J, Godet, E, Forlani, S, Melki, J, Auer-Grumbach, M, Fernandez, J C, Martin-Hardy, P, Sibon, I, Sole, G, Orignac, I, Mhiri, C, Coutinho, P, Durr, A, Brice, A, Stevanin, G

“…Hereditary spastic paraplegias (HSPs) are very heterogeneous inherited neurodegenerative disorders. Our group recently identified ZFYVE26 as the gene…”
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Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity by Boukhris, A, Stevanin, G, Feki, I, Denora, P, Elleuch, N, Miladi, MI, Goizet, C, Truchetto, J, Belal, S, Brice, A, Mhiri, C

“…Hereditary spastic paraplegias (HSP) constitute a clinically and genetically heterogeneous group of neurodegenerative disorders characterized by slowly…”
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Prevalence and distribution of Helicobacter pylori cagA and vacA genotypes in the Moroccan population with gastric disease by Boukhris, S. A., Benajah, D.-a., El Rhazi, K., Ibrahimi, S. A., Nejjari, C., Amarti, A., Mahmoud, M., El Abkari, M., Souleimani, A., Bennani, B.

“…Helicobacter pylori infection is the etiologic agent of various gastric pathologies. The severity of disease outcome has been attributed to some H. pylori…”
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Selective bilateral thalamic necrosis following carbon monoxide poisoning: Case report by Abdelhedi, J, Bouchhima, I, Turki, E, Damak, M, Boukhris, A, Miladi, M.I, Fki, I, Mhiri, C

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Characteristics of motor complications in patients with Parkinson's/INS; disease in southern Tunisia (ST) by Smaoui, S, Boukhris, A, Damak, M, Turki, E, Bouchhima, I, Miladi, M.I, Feki, I, Mhiri, C

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Atypical neurological presentation of GSS: Case report by Daoud, O.H, Hdiji, O, Bouchhima, I, Turki, E, Boukhris, A, Damak, M, Miladi, M.I, Feki, I, Mhiri, C

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Characteristics of Parkinson's disease dementia in Southern Tunisia by Smaoui, S, Boukhris, A, Damak, M, Turki, E, Bouchhima, I, Miladi, M.I, Feki, I, Mhiri, C

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P03-528 - Depression, anxiety and multiple sclerosis: Links with alexithymia by Aloulou, J, Hachicha, C, Masmoudi, R, Boukhris, A, Mhiri, C, Amami, O

“…The aim of our study was to assess the prevalence of depression and anxiety in a population of patients treated for multiple sclerosis (MS) and their link with…”
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PO19-WE-06 New mutation in ATP7B gene associated with severe neurological symptoms by Elleuch, N, Bouchhima, I, Feki, I, Turki, E, Boukhris, A, Damak, M, Miladi, M.I, Chappuis, P, Woimant, F, Mhiri, C

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FP31-WE-04 Complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum: a new locus and further genetic heterogeneity by Boukhris, A, Feki, I, Elleuch, N, Miladi, M.I, Forlani, S, Belal, S, Brice, A, Mhiri, C, Stavanin, G

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Familial spastic paraplegia with severe amyotrophy of the hands. (Silver syndrome?) by Feki, I, Miladi, M I, Elleuch, N, Boukhris, A, Stévanin, G, Brice, A, Mhiri, C

“…Familial spastic paraplegia (FSP) with severe muscular atrophy of hands and feet is exceptional. Autosomal dominant forms were initially described by Silver in…”
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Features of hereditary spastic paraplegias in North African region by Mhiri, C., Boukhris, A., Stevanin, G., Brice, A.

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A novel mutation in ATP7B gene associated with severe neurological impairment in Wilson's disease by Elleuch, N, Feki, I, Turki, E, Miladi, M I, Boukhris, A, Damak, M, Mhiri, C, Chappuis, E, Woimant, F

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Nouvelle mutation du gène ATP7B responsable d’une maladie de Wilson avec atteinte neurologique sévère by Elleuch, N., Feki, I., Turki, E., Miladi, M.I., Boukhris, A., Damak, M., Mhiri, C., Chappuis, E., Woimant, F.

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Electron density in ammonium dihydrogen phosphate: non-uniqueness of the multipolar model in simple inorganic structures by Pérès, N., Boukhris, A., Souhassou, M., Gavoille, G., Lecomte, C.

“…X‐ray and neutron diffraction data of a single crystal of ammonium dihydrogen phosphate have been used for the determination of the electron density using…”
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Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome by 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

“…Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous disorders. Both “uncomplicated” and “complicated” forms have been…”
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Paraplégie spastique familiale avec amyotrophie sévère des mains (syndrome de Silver?) by Feki, I., Miladi, M.I., Elleuch, N., Boukhris, A., Stévanin, G., Brice, A., Mhiri, C.

“…Les paraplégies spastiques familiales (PSF) avec amyotrophie sévère des mains et des pieds sont exceptionnelles. Des formes de transmission autosomique…”
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Mitochondrial Morpho-Functional Dysfunction in SPG31 Patients (IN7-1.007) by Goizet, C., Benard, G., Depienne, C., Boukhris, A., Sole, G., Coupry, I., Pilliod, J., Martin-Negrier, M.-L., Forlani, S., Durr, A., Brice, A., Lacombe, D., Rossignol, R., Stevanin, G.

“…Abstract only…”
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