Search Results - "Benhamida, M."

Structural and elastic properties of ternary metal nitrides TixTa1−xN alloys: First-principles calculations versus experiments by Djemia, P., Benhamida, M., Bouamama, Kh, Belliard, L., Faurie, D., Abadias, G.

“…First-principles pseudopotential calculations of the lattice constants and of the single-crystal elastic constants for TixTa1−xN (0≤x≤1) alloys with…”
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Locked posterior dislocation of the shoulder: A report of three cases by Benhamida, M.K., Ouertatani, M., Hasayri, I., Benhassine, A., Meherzi, M., Bouhdiba, S., Mestiri, M.

“…Posterior shoulder dislocations account for 4% of all shoulder dislocations. In two-thirds of the cases, the diagnosis is made only once the shoulder is…”
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L’otite externe nécrosante chez le diabétique : quelles particularités ? by Benhamida, M., Ben Mabrouk, A., Hasnaoui, M., Elomma Mrabet, H., Chebil, E., Bougossa, R., Chelli, J., Larbi, F.

“…L’otite externe nécrosante est une infection progressive du canal auditif externe et de la base du crâne. Elle s’observe principalement chez les sujets…”
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International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome by TROUILLAS, P, TAKAYANAGI, T, COUTINHO, P, HAMIDA, M. B, CAMPANELLA, G, FILLA, A, SCHUT, L, TIMANN, D, HONNORAT, J, NIGHOGHOSSIAN, N, MANYAM, B, HALLETT, M, CURRIER, R. D, SUBRAMONY, S. H, WESSEL, K, BRYER, A, DIENER, H. C, MASSAQUOI, S, GOMEZ, C. M

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Bronchiolite : faire aussi bien en prescrivant moins by Benhamida, M., Verstraete, M., Bihouee, T., Launay, E., Gras le Guen, C.

“…Paru en 2012, le consensus sur la prise en charge de la bronchiolite des enfants de moins de 1 an des CHU du Grand-Ouest propose une limitation des examens…”
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Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein by Mandel, Jean-Louis, Inoue, Keizo, Arai, Hiroyuki, Arita, Makoto, Hentati, Fayçal, Hamida, Mongi Ben, Koenig, Michel, Ouahchi, Karim, Sokol, Ronald, Kayden, Herbert

“…Ataxia with isolated vitamin E deficiency (AVED) is an autosomal recessive neurodegenerative disease which maps to chromosome 8q13. AVED patients have an…”
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Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy by Noguchi, Satoru, McNally, Elizabeth M., Ben Othmane, Kamel, Hagiwara, Yasuko, Mizuno, Yuji, Yoshida, Mikiharu, Yamamoto, Hideko, Bönnemann, Carsten G., Gussoni, Emanuela, Denton, Peter H., Kyriakides, Theodoros, Middleton, Lefkos, Hentati, Faycal, Ben Hamida, Mongi, Nanoka, Ikuya, Vance, Jeffery M., Kunkel, Louis M., Ozawa, Eijiro

“…Severe childhood autosomal recessive muscular dystrophy (SCARMD) is a progressive muscle-wasting disorder common in North Africa that segregates with…”
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Large wind turbine generators: State-of-the-art review by Bensalah, A., Benhamida, M. A., Barakat, G., Amara, Y.

“…This paper presents a broad overview of wind energy conversion generators in muti-megawatts wind turbines. Both technological and economic advantages and…”
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Reluctance network - Lumped mechanical & thermal models for the modeling of concentrated flux synchronous machine by Benhamida, M. A., Ennassiri, H., Amara, Y., Barakat, G.

“…The aim of this paper is the multi-physical modeling of synchronous permanent magnet machines using reluctance network, lumped mechanical & thermal models…”
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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35 by Bejaoui, Khemissa, Pericak-Vance, Margaret A, Hentati, Afif, Brown, Robert H, Hung, Wu-Yen, Siddique, Teepu, Speer, Marcy C, Ben Hamida, Christiane, Ben Hamida, Mongi, Hentati, Faycal, Figlewicz, Denise A, Haines, Jonathan, Rimmler, Jackie

“…Amyotrophic lateral sclerosis (ALS) usually presents as a sporadic disorder of motor neurons. However, familial forms of ALS have been described--autosomal…”
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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 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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Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease by Hamzaoui, K, Hamzaoui, A, Hentati, F, Kahan, A, Ayed, K, Chabbou, A, Ben Hamida, M, Hamza, M

“…Our aim was to investigate the TCR gamma delta+ subset in Behçet's disease (BD) inflammatory sites, which better reflects changes associated with the…”
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Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy by Ben Hamida, M, Hentati, F, Ben Hamida, C

“…Forty-three patients with hereditary motor system diseases belonging to 17 families were studied. The clinical features consisted of a bilateral pyramidal…”
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Vibrational behavior investigation approach and Influence of contact coefficient on stator natural frequencies by Ennassiri, H., Benhamida, M. A., Amara, Y., Barakat, G., Paulides, J. H.

“…This paper presents a summary of a vibrational behavior investigation of a 27 slots / 24 poles combination surface mounted synchronous electric motor. To…”
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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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Prevalence of epilepsy in Kelibia, Tunisia by Attia-Romdhane, N, Mrabet, A, Ben Hamida, M

“…A door-to-door survey was made in Kelibia, Tunisia to determine the prevalence of major neurologic disorders, including epilepsy. The survey was made according…”
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Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers by Hentati, A, Pericak-Vance, M A, Lennon, F, Wasserman, B, Hentati, F, Juneja, T, Angrist, M H, Hung, W Y, Boustany, R M, Bohlega, S

“…'Pure' autosomal dominant familial spastic paraplegia (SPG) is a neurodegenerative disease which clinically manifests as spasticity of the lower limbs…”
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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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