Search Results - "Hamida, C"

Safety and efficacy of colistin compared with imipenem in the treatment of ventilator-associated pneumonia : a matched case-control study by KALLEL, H, HERGAFI, L, BAHLOUL, M, HAKIM, A, DAMMAK, H, CHELLY, H, BEN HAMIDA, C, CHAARI, A, REKIK, N, BOUAZIZ, M

“…Our study aimed to determine the efficacy and safety of colistin in the treatment of ventilator-associated pneumonia (VAP) caused by pan-drug-resistant…”
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Safety and efficacy of colistin compared with imipenem in the treatmentof ventilator-associated pneumonia: a matched case–control study by Kallel, H., Hergafi, L., Bahloul, M., Hakim, A., Dammak, H., Chelly, H., Hamida, C. Ben, Chaari, A., Rekik, N., Bouaziz, M.

“…Our study aimed to determine the efficacy and safety of colistin in the treatment of ventilator-associated pneumonia (VAP) caused by pan-drug-resistant…”
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Replicative potential and telomere length in human skeletal muscle: implications for satellite cell-mediated gene therapy by Decary, S, Mouly, V, Hamida, C B, Sautet, A, Barbet, J P, Butler-Browne, G S

“…In this study, we have evaluated the ability of human satellite cells isolated from subjects aged from 5 days to 86 years to proliferate in culture. Cells were…”
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Prevalence of hospital-acquired infection in a Tunisian hospital by Kallel, H., Bahoul, M., Ksibi, H., Dammak, H., Chelly, H., Hamida, C.B., Chaari, A., Rekik, N., Bouaziz, M.

“…In order to estimate the prevalence of hospital-acquired infection (HAI) and research factors associated with its occurrence, a one-day prevalence survey was…”
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Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) by Hammouda, Hadi, Nicole, Sophie, Topaloglu, Haluk, Weissenbach, Jean, Lehmann-Horn, Franck, Samson, Delphine, Cruaud, Corinne, Hentati, Faycal, Davoine, Claire-Sophie, Beighton, Peter, Barral, Duarte, Fontaine, Bertrand, Urtizberea, J. Andoni, White, Peter S, Cattolico, Laurence, Hamida, Christiane Ben

“…Schwartz-Jampel syndrome (SJS1) is a rare autosomal recessive disorder characterized by permanent myotonia (prolonged failure of muscle relaxation) and…”
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Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children by Decary, S, Hamida, C B, Mouly, V, Barbet, J P, Hentati, F, Butler-Browne, G S

“…Muscular dystrophies are characterised by continuous cycles of degeneration and regeneration resulting in an eventual diminution of the muscle mass and…”
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Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family by MRISSA, N, BELAL, S, BEN HAMIDA, C, AMOURI, R, TURKI, I, MRISSA, R, BEN HAMIDA, M, HENTATI, F

“…To report the clinical findings and the genetic linkage mapping of an autosomal recessive cerebellar ataxia associated to peripheral neuropathy, showing an…”
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A good death: another break in the wall by Kallel, H, Dammak, H, Bahloul, M, Ben Hamida, C, Chelly, H, Rekik, N, Bouaziz, M

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Evaluation of the pesticide Oberon on a model organism Drosophila melanogaster via topical toxicity test on biochemical and reproductive parameters by Kissoum, N., Bensafi-Gheraibia, H., Hamida, Z.C., Soltani, N.

“…Spiromesifen (Oberon® 240 SC), a pesticide widely used to control pests like mites and whiteflies, was investigated using Drosophila melanogaster Meigen, 1830…”
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Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping by Dib, C, Belal, S, Cohen, D, Novelli, G, Reutenauer, L, Ben Hamida, C, Mandel, J.-L, Linder, C, Vignal, A, Gyapay, G, Doerflinger, N, Hentati, F, Mokini, V, Kœnig, M, Le Paslier, D, Ben Hamida, M, Pandolfo, M

“…Friedreich ataxia and ataxia with selective vitamin E deficiency (AVED) share very similar clinical phenotypes. We have mapped the AVED locus to proximal 8q…”
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The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy by 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

“…Disorganization of the neurofilament network is a prominent feature of several neurodegenerative disorders including amyotrophic lateral sclerosis (ALS),…”
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Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q by Ben Othmane, K, Hentati, F, Lennon, F, Ben Hamida, C, Blel, S, Roses, A D, Pericak-Vance, M A, Ben Hamida, M, Vance, J M

“…Autosomal recessive Charcot-Marie-Tooth (CMT) disease (CMT4) is a complex group of severe childhood motor and sensory neuropathies, characterized by an early…”
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Pre-imaginal exposure to Oberon® disrupts fatty acid composition, cuticular hydrocarbon profile and sexual behavior in Drosophila melanogaster adults by Hamida, Z.C., Farine, J.P., Ferveur, J.F., Soltani, N.

“…Oberon® is a commercial formulation of spiromesifen, a pesticide inhibitor of lipid biosynthesis via acetyl CoA carboxylase, widely used in agricultural crop…”
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Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation by Kefi, M, Amouri, R, Driss, A, Ben Hamida, C, Ben Hamida a, M, Kunkel, L.M, Hentati, F

“…Limb-girdle muscular dystrophy type 2C is an autosomal recessive muscular disorder caused by mutations in the gene encoding the γ-sarcoglycan subunit. This…”
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Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14 by BEJAOUI, K, HIRABAYASHI, K, GRIGGS, R. C, MUNSAT, T. L, BEN HAMIDA, M, ARAHATA, K, BROWN, R. H, HENTATI, F, HAINES, J. L, BEN HAMIDA, C, BELAL, S, MILLER, R. G, MCKENNA-YASEK, D, WEISSENBACH, J, ROWLAND, L. P

“…Miyoshi myopathy (MM) is a young-adult-onset, autosomal recessive distal muscular dystrophy initially affecting the plantar flexors. We analyzed 12 MM…”
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Friedreich's ataxia with isolated vitamin E deficiency : a neuropathological study of a Tunisian patient by LARNAOUT, A, BELAL, S, ZOUARI, M, FKI, M, HAMIDA, C. B, GOEBEL, H. H, BEN HAMIDA, M, HENTATI, F

“…The neuropathological findings in a Tunisian patient with Friedreich's ataxia with vitamin E deficiency are reported. The main histological changes are: (1)…”
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A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3 by Driss, A., Amouri, R., Ben Hamida, C., Souilem, S., Gouider-Khouja, N., Ben Hamida, M., Hentati, F.

“…Autosomal recessive limb-girdle muscular dystrophies represent a genetically heterogeneous group of diseases characterized by a progressive involvement of…”
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Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3 by Barhoumi, C, Amouri, R, Ben Hamida, C, Ben Hamida, M, Machghoul, S, Gueddiche, M, Hentati, F

“…We report the clinical and genetic linkage analysis of a large Tunisian family with thirteen affected patients suffering from Charcot–Marie–Tooth disease with…”
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Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families by Ben Hamida, M, Belal, S, Sirugo, G, Ben Hamida, C, Panayides, K, Ionannou, P, Beckmann, J, Mandel, J L, Hentati, F, Koenig, M

“…Friedreich's ataxia (FA) is an autosomal recessive neurodegenerative disorder, the disease locus (FRDA) of which has been assigned to 9q13-q21.1 by genetic…”
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Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency by Zouari, M, Feki, M, Ben Hamida, C, Larnaout, A, Turki, I, Belal, S, Mebazaa, A, Ben Hamida, M, Hentati, F

“…The authors report a comparative study of peripheral nerve conductions and nerve biopsy and somatosensory evoked potentials between 15 patients with…”
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