Search Results - "Hamri, A"

Giant, Voltage Tuned, Quality Factors of Single Wall Carbon Nanotubes and Graphene at Room Temperature by Descombin, A, Poncharal, P, Pascale-Hamri, A, Choueib, M, Diehl, R, Vincent, P, Purcell, S. T, Ayari, A, Perisanu, S

“…Mastering dissipation in graphene-based nanostructures is still the major challenge in most fundamental and technological exploitations of these ultimate…”
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Ultrashort single-wall carbon nanotubes reveal field-emission coulomb blockade and highest electron-source brightness by Pascale-Hamri, A, Perisanu, S, Derouet, A, Journet, C, Vincent, P, Ayari, A, Purcell, S T

“…We present here well-defined Coulomb staircases using an original field-emission experiment on several individual in situ-grown single-wall carbon nanotubes. A…”
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Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients by Anheim, M., Monga, B., Fleury, M., Charles, P., Barbot, C., Salih, M., Delaunoy, J. P., Fritsch, M., Arning, L., Synofzik, M., Schöls, L., Sequeiros, J., Goizet, C., Marelli, C., Le Ber, I., Koht, J., Gazulla, J., De Bleecker, J., Mukhtar, M., Drouot, N., Ali-Pacha, L., Benhassine, T., Chbicheb, M., M’Zahem, A., Hamri, A., Chabrol, B., Pouget, J., Murphy, R., Watanabe, M., Coutinho, P., Tazir, M., Durr, A., Brice, A., Tranchant, C., Koenig, M.

“…Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disease due to mutations in the senataxin gene, causing progressive cerebellar ataxia…”
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Wear rate control of peek surfaces modified by femtosecond laser by Hammouti, S., Pascale-Hamri, A., Faure, N., Beaugiraud, B., Guibert, M., Mauclair, C., Benayoun, S., Valette, S.

“…•Tribological properties of a laser surface texturing on PEEK was investigated.•Dimpled surfaces exhibited the highest friction coefficients.•Wear rates of…”
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Magnetic ordering in RPtBi topological insulators from DFT+U calculations by Hallouche, A., Hamri, A., Kacimi, S., Zaoui, A.

“…We report on the detailed electronic properties of half Heusler compounds RPtBi (R=La, Gd, Lu). LDA+U predict an anti-ferromagnetic GdPtBi and nonmagnetic…”
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Elaboration of submicron structures on PEEK polymer by femtosecond laser by Hammouti, S., Beaugiraud, B., Salvia, M., Mauclair, C., Pascale-Hamri, A., Benayoun, S., Valette, S.

“…•We compare PEEK polymer under two crystalline forms: semi-crystalline and amorphous.•We assess topographical modifications of surface morphologies after…”
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Comparison of four technics of surface roughness assessment of corneal lamellar cuts by Gain, P., Jumelle, C., Hamri, A., Egaud, G., Mauclair, C., Reynaud, S., Dumas, S., Pereira, S., Thuret, G.

“…Purpose Surface roughness of corneal lamellar cuts is a crucial quality criterion, because smother is the cutting plan, better will be the visual recovery…”
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Limbic encephalitis associated with glutamic acid decarboxylase antibodies in a young adolescent by M’zahem, A., Meziani, A., Taghane, N., Boulefkhad, A., Khellaf, S., Hamri, A.

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Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients by Tazir, M, Ali-Pacha, L, M'Zahem, A, Delaunoy, J.P, Fritsch, M, Nouioua, S, Benhassine, T, Assami, S, Grid, D, Vallat, J.M, Hamri, A, Koenig, M

“…Abstract Ataxia with oculo-motor apraxia type 2 (AOA2) is a recently described autosomal recessive cerebellar ataxia (ARCA) caused by mutations in the…”
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The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa by RICHARD, P, GAUDON, K, HAMRI, A, NOUIOUA, S, TAZIR, M, MAYER, M, DESNUELLE, C, BAROIS, A, CHABROL, B, POUGET, J, KOENIG, J, GOUIDER-KHOUJA, N, HADDAD, H, HENTATI, F, EYMARD, B, HANTAÏ, D, BEN AMMAR, A, GENIN, E, BAUCHE, S, PATURNEAU-JOUAS, M, MÜLLER, J. S, LOCHMÜLLER, H, GRID, D

“…Mutations in various genes of the neuromuscular junction cause congenital myasthenic syndrome (CMS). A single truncating mutation (epsilon1293insG) in the…”
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Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays by H’mida-Ben Brahim, D., M’zahem, A., Assoum, M., Bouhlal, Y., Fattori, F., Anheim, M., Ali-Pacha, L., Ferrat, F., Chaouch, M., Lagier-Tourenne, C., Drouot, N., Thibaut, C., Benhassine, T., Sifi, Y., Stoppa-Lyonnet, D., N’Guyen, K., Poujet, J., Hamri, A., Hentati, F., Amouri, R., Santorelli, F. M., Tazir, M., Koenig, M.

“…The diagnosis of rare inherited diseases is becoming more and more complex as an increasing number of clinical conditions appear to be genetically…”
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Clinical Analysis of Algerian Patients with Pompe Disease by Sifi, Y., Medjroubi, M., Froissart, R., Taghane, N., Sifi, K., Benhabiles, A., Lemai, S., Semra, S., Benmekhebi, H., Bouderda, Z., Abadi, N., Hamri, A.

“…Pompe’s disease is a metabolic myopathy caused by a deficiency of acid alpha-glucosidase (GAA), also called acid maltase, an enzyme that degrades lysosomal…”
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O.21 Genetic characterisation of PHARC – a novel syndrome resembling Refsum’s disease by Bindoff, L.A, Fiskerstrand, T, Brahim, D. H’mida-Ben, Johansson, S, M’zahem, A, Haukanes, B.I, Drouot, N, Zimmermann, J, Cole, A.J, Vedeler, C, Bredrup, C, Assoum, M, Tazir, M, Klockgether, T, Hamri, A, Steen, V.M, Boman, H, Koenig, M, Knappskog, P.M

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Clinical and Genetic Study of Algerian Patients with Spinal Muscular Atrophy by Sifi, Y., Sifi, K., Boulefkhad, A., Abadi, N., Bouderda, Z., Cheriet, R., Magen, M., Bonnefont, J. P., Munnich, A., Benlatreche, C., Hamri, A.

“…Spinal muscular atrophy (SMA) is the second most common lethal autosomal recessive disorder. It is divided into the acute Werdnig-Hoffmann disease (type I),…”
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Influence of pulse repetition rate on morphology and material removal rate of ultrafast laser ablated metallic surfaces by Sedao, X., Lenci, M., Rudenko, A., Faure, N., Pascale-Hamri, A., Colombier, J.P., Mauclair, C.

“…•The removal rate and surface roughness of ultrafast laser machining of metallic materials (Ni, Cu, stainless steel 316L and Ti-based alloy TA6V) are…”
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Ab-initio study of the electronic structure and magnetic properties of ACr2Pn2 (A =Ba, Sr, Ca, Sc, K; Pn=As, P) by Hamri, A.K., Djermouni, M., Zaoui, A., Kacimi, S.

“…We study the electronic structure and magnetic interactions of ten layered chromium tetragonal pnictides ACr2Pn2 (A = Ba, Sr, Ca, Sc, K, and Pn = As, P) using…”
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Stereotactic radiosurgery at St. Bartholomew's hospital: third quinquennial review by El Hamri, A K, Monk, J, Plowman, P N

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Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism by Fiskerstrand, Torunn, H'mida-Ben Brahim, Dorra, Johansson, Stefan, M'zahem, Abderrahim, Haukanes, Bjørn Ivar, Drouot, Nathalie, Zimmermann, Julian, Cole, Andrew J., Vedeler, Christian, Bredrup, Cecilie, Assoum, Mirna, Tazir, Meriem, Klockgether, Thomas, Hamri, Abdelmadjid, Steen, Vidar M., Boman, Helge, Bindoff, Laurence A., Koenig, Michel, Knappskog, Per M.

“…Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract (PHARC) is a neurodegenerative disease marked by early-onset cataract and hearing…”
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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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Influence of initial conditions on the optical and electrical characterisation of sillenite-type crystals by Hamri, A., Secu, M., Topa, V., Briat, B.

“…We compare a set of results concerning our measurement of the optical absorption (OA), photoconductivity (PC), thermally stimulated currents (TSC) and…”
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