Search Results - "HAMIDA, C. B"

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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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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Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy by Hamida, C B, Soussi-Yanicostas, N, Bejaoui, K, Butler-Browne, G S, Hentati, F, Ben Hamida, M

“…Morphological, morphometrical, histoenzymological, immunocytochemical and biochemical analysis were performed on muscle biopsies taken from patients suffering…”
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Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C) by Ben Othmane, K, Speer, M C, Stauffer, J, Blel, S, Middleton, L, Ben Hamida, C, Etribi, A, Loeb, D, Hentati, F, Roses, A D

“…Duchenne-like muscular dystrophy (DLMD) is an autosomal recessive Limb Girdle muscular dystrophy (LGMD2C) whose phenotype closely resembles X-linked Duchenne…”
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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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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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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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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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Factors Associated with Pulmonary Edema in Severe Scorpion Sting Patients - A Multivariate Analysis of 428 Cases by Bouaziz, Mounir, Bahloul, Mabrouk, Hergafi, Leila, Kallel, Hatem, Chaari, Leila, Ben Hamida, Chokri, Chaari, Adel, Chelly, Hedi, Rekik, Noureddine

“…Objective. To determine clinical and routine laboratory factors associated with pulmonary edema secondary to scorpion envenomation. Design and Setting…”
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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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Colistin as a salvage therapy for nosocomial infections caused by multidrug-resistant bacteria in the ICU by Kallel, Hatem, Bahloul, Mabrouk, Hergafi, Leila, Akrout, Malek, Ketata, Wajdi, Chelly, Hedi, Hamida, Chokri Ben, Rekik, Noureddine, Hammami, Adnane, Bouaziz, Mounir

“…The objective of this study was to determine the efficacy of systemic colistin therapy in the treatment of nosocomial infections caused by multidrug-resistant…”
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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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Structural and ultrastructural quantitative study of skin and nerve biopsies in the diagnosis of congenital indifference to pain by Hamida, C B, Samouda, F

“…The muscolo-cutaneous nerve, and skin biopsies from 3rd and 5th finger-tips and the back were studied in a 8-year-old girl with congenital indifference to…”
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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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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q by Ben Othmane, Kamel, Ben Hamida, Mongi, Pericak-Vance, Margaret A, Ben Hamida, Christiane, Blel, Samir, Carter, Susan C, Bowcock, Anne M, Petruhkin, Konstantin, Conrad Gilliam, T, Roses, Allen D, Hentati, Faycal, Vance, Jeffery M

“…Autosomal recessive Duchenne-like muscular dystrophy (DLMD) is a severe dystrophic myopathy. The incidence is unknown because of its clinical similarity to…”
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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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Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping by Nicole, S, Ben Hamida, C, Beighton, P, Bakouri, S, Belal, S, Romero, N, Viljoen, D, Ponsot, G, Sammoud, A, Weissenbach, J

“…Schwartz-Jampel syndrome (SJS, MIM 255800), also known as chondrodystrophic myotonia, is a rare autosomal recessive disorder characterized by generalized…”
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Adhalin deficiency by Hamida, Christiane Ben

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Ataxia with vitamin E deficiency : refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families by DOERFLINGER, N, LINDER, C, MONGI BEN HAMIDA, PANDOLFO, M, DIDONATO, S, SOKOL, R, KAYDEN, H, LANDRIEU, P, DURR, A, BRICE, A, GOUTIERES, F, KOHLSCHÜTTER, A, OUAHCHI, K, SABOURAUD, P, ALI BENOMAR, MOHAMED YAHYAOUI, MANDEL, J.-L, KOENIG, M, GYAPAY, G, WEISSENBACH, J, LE PASLIER, D, RIGAULT, P, SAMIR BELAL, BEN HAMIDA, C, HENTATI, F

“…Ataxia with vitamin E deficiency (AVED) is an autosomal recessive disease characterized clinically by neurological symptoms with often striking resemblance to…”
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Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1 by Ben Hamida, C, Cavalier, L, Belal, S, Sanhaji, H, Nadal, N, Barhoumi, C, M'Rissa, N, Marzouki, N, Mandel, J L, Ben Hamida, M, Koenig, M, Hentati, F

“…Giant axonal neuropathy (GAN) is a rare autosomal recessive disorder described as a symmetrical distal neuropathy, with peripheral axons dilated by…”
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