Prevalence of hospital-acquired infection in a Tunisian hospital
Kallel, H., Bahoul, M., Ksibi, H., Dammak, H., Chelly, H., Hamida, C.B., Chaari, A., Rekik, N., Bouaziz, M.
Published in The Journal of hospital infection (01.04.2005)
Published in The Journal of hospital infection (01.04.2005)
Get full text
Journal Article
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
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
Published in Human molecular genetics (01.10.1993)
Published in Human molecular genetics (01.10.1993)
Get more information
Journal Article
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy
Ben Hamida, C., Soussi-Yanicostas, N., Bejaoui, K., Butler-Browne, G.S., Hentati, F., Ben Hamida, M.
Published in Journal of the neurological sciences (01.05.1994)
Published in Journal of the neurological sciences (01.05.1994)
Get full text
Journal Article
Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)
Ben Othmane, K, Speer, M C, Stauffer, J, Blel, S, Middleton, L, Ben Hamida, C, Etribi, A, Loeb, D, Hentati, F, Roses, A D
Published in American journal of human genetics (01.09.1995)
Get full text
Published in American journal of human genetics (01.09.1995)
Journal Article
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)
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
Published in Nature genetics (01.12.2000)
Published in Nature genetics (01.12.2000)
Get full text
Journal Article
Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children
Decary, S, Hamida, C B, Mouly, V, Barbet, J P, Hentati, F, Butler-Browne, G S
Published in Neuromuscular disorders : NMD (01.02.2000)
Published in Neuromuscular disorders : NMD (01.02.2000)
Get full text
Journal Article
Safety and efficacy of colistin compared with imipenem in the treatmentof ventilator-associated pneumonia: a matched case–control study
Kallel, H., Hergafi, L., Bahloul, M., Hakim, A., Dammak, H., Chelly, H., Hamida, C. Ben, Chaari, A., Rekik, N., Bouaziz, M.
Published in Intensive care medicine (01.07.2007)
Published in Intensive care medicine (01.07.2007)
Get full text
Journal Article
Factors Associated with Pulmonary Edema in Severe Scorpion Sting Patients - A Multivariate Analysis of 428 Cases
Bouaziz, Mounir, Bahloul, Mabrouk, Hergafi, Leila, Kallel, Hatem, Chaari, Leila, Ben Hamida, Chokri, Chaari, Adel, Chelly, Hedi, Rekik, Noureddine
Published in Clinical toxicology (Philadelphia, Pa.) (01.01.2006)
Published in Clinical toxicology (Philadelphia, Pa.) (01.01.2006)
Get full text
Journal Article
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
Mrissa, N, Belal, S, Hamida, C B, Amouri, R, Turki, I, Mrissa, R, Hamida, M B, Hentati, F
Published in Neurology (11.04.2000)
Published in Neurology (11.04.2000)
Get more information
Journal Article
Colistin as a salvage therapy for nosocomial infections caused by multidrug-resistant bacteria in the ICU
Kallel, Hatem, Bahloul, Mabrouk, Hergafi, Leila, Akrout, Malek, Ketata, Wajdi, Chelly, Hedi, Hamida, Chokri Ben, Rekik, Noureddine, Hammami, Adnane, Bouaziz, Mounir
Published in International journal of antimicrobial agents (01.10.2006)
Published in International journal of antimicrobial agents (01.10.2006)
Get full text
Journal Article
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
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
Published in Nature genetics (01.11.2000)
Published in Nature genetics (01.11.2000)
Get full text
Journal Article
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
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
Published in Nature genetics (01.10.1993)
Published in Nature genetics (01.10.1993)
Get full text
Journal Article
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q
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
Published in Nature genetics (01.12.1992)
Published in Nature genetics (01.12.1992)
Get full text
Journal Article
Friedreich's ataxia with isolated vitamin E deficiency : a neuropathological study of a Tunisian patient
LARNAOUT, A, BELAL, S, ZOUARI, M, FKI, M, HAMIDA, C. B, GOEBEL, H. H, BEN HAMIDA, M, HENTATI, F
Published in Acta neuropathologica (01.06.1997)
Published in Acta neuropathologica (01.06.1997)
Get full text
Journal Article
Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping
Nicole, S, Ben Hamida, C, Beighton, P, Bakouri, S, Belal, S, Romero, N, Viljoen, D, Ponsot, G, Sammoud, A, Weissenbach, J
Published in Human molecular genetics (01.09.1995)
Published in Human molecular genetics (01.09.1995)
Get more information
Journal Article
Ataxia with vitamin E deficiency : refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families
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
Published in American journal of human genetics (01.05.1995)
Get full text
Published in American journal of human genetics (01.05.1995)
Journal Article
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
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
Published in Neurogenetics (01.11.1997)
Published in Neurogenetics (01.11.1997)
Get full text
Journal Article