Search Results - "Tazir, M"

CICP: Cluster Iterative Closest Point for sparse–dense point cloud registration by Lamine Tazir, M., Gokhool, Tawsif, Checchin, Paul, Malaterre, Laurent, Trassoudaine, Laurent

“…Point cloud registration is an important and fundamental building block of mobile robotics. It forms an integral part of the processes of mapping,…”
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Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families by Kediha, M.I., Tazir, M., Sternberg, D., Eymard, B., Ali Pacha, L.

“…Congenital myasthenic syndromes (CMS) are a heterogeneous group of rare genetic disorders. The acetyl choline receptor contains five subunits, with a…”
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COMPARISON OF UAV LIDAR ODOMETRY OF ROTATING AND FIXED VELODYNE PLATFORMS by Tazir, M. L., Seube, N.

“…Three-dimensional LiDAR rangefinders are increasingly integrated into unmanned aerial vehicles (UAV), due to their direct access to 3D information, their high…”
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Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families by Kediha, M.I., Tazir, M., Magnouche, C., Sternberg, D., Belarbi, S., Eymard, B., Ali Pacha, L.

“…Congenital myasthenic syndromes (CMS) are rare genetic neuromuscular disorders. The COLQ gene encoding the collagenous subunit of the acetyl cholinesterase…”
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High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in Algiers by Antri, K., Rouzic, N., Dauwalder, O., Boubekri, I., Bes, M., Lina, G., Vandenesch, F., Tazir, M., Ramdani-Bouguessa, N., Etienne, J.

“…USA300 is an epidemic community-acquired methicillin-resistant Staphylococcus aureus (C-MRSA) clone in the USA, whereas the European C-MRSA clone ST80-IV has…”
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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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Classifications of neurogenetic diseases: An increasingly complex problem by Vallat, J.-M., Goizet, C., Tazir, M., Couratier, P., Magy, L., Mathis, S.

“…Neurodegenerative disorders represent a wide group of diseases affecting the central and/or peripheral nervous system. Many of these disorders were described…”
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Creatine deficiency syndrome. A treatable myopathy due to arginine–glycine amidinotransferase (AGAT) deficiency by Nouioua, S, Cheillan, D, Zaouidi, S, Salomons, G.S, Amedjout, N, Kessaci, F, Boulahdour, N, Hamadouche, T, Tazir, M

“…Abstract We report two sisters, aged 11 and 6 years, with AGAT deficiency syndrome (OMIM 612718 ) which is the least common creatine deficiency syndrome. They…”
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MUTATIONS IN THE GLUCOCEREBROSIDASE GENE CONFER A RISK FOR PARKINSON DISEASE IN NORTH AFRICA by LESAGE, S, CONDROYER, C, TAZIR, M, BRICE, A, HECHAM, N, ANHEIM, M, BELARBI, S, LOHMAN, E, VIALLET, F, POLLAK, P, ABADA, M, DÜRR, A

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations by AZZEDINE, H, RAVISE, N, HAMADOUCHE, T, BOUHOUCHE, A, GUILBOT, A, STENDEL, C, RUBERG, M, BRICE, A, BIROUK, N, DUBOURG, O, TAZIR, M, LEGUERN, E, VERNY, C, GABRËELS-FESTEN, A, LAMMENS, M, GRID, D, VALLAT, J. M, DUROSIER, G, SENDEREK, J, NOUIOUA, S

“…Charcot-Marie-Tooth (CMT) disease is a heterogeneous group of inherited peripheral motor and sensory neuropathies with several modes of inheritance: autosomal…”
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IS THE COMMON LRRK2 G2019S MUTATION RELATED TO DYSKINESIAS IN NORTH AFRICAN PARKINSON DISEASE? by LESAGE, S, BELARBI, S, TAZIR, M, BRICE, A, TROIANO, A, CONDROYER, C, HECHAM, N, POLLAK, P, LOHMAN, E, BENHASSINE, T, YSMAIL-DAHLOUK, F, DÜRR, 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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Autosomal recessive cerebellar ataxia: A clinical and genetic study by Hamza, W, Nouioua, S, Lagier-Tourenne, C, Assami, S, Benhassine, T, Koenig, M, Tazir, M

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Evolution of antimicrobial resistance and serotype distribution of Streptococcus pneumoniae isolated from children with invasive and noninvasive pneumococcal diseases in Algeria from 2005 to 2012 by Ramdani-Bouguessa, N, Ziane, H, Bekhoucha, S, Guechi, Z, Azzam, A, Touati, D, Naim, M, Azrou, S, Hamidi, M, Mertani, A, Laraba, A, Annane, T, Kermani, S, Tazir, M

“…Abstract Pneumococcal infections are a major cause of morbidity and mortality in developing countries. The introduction of pneumococcal conjugate vaccines…”
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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease by Dubourg, O, Azzedine, H, Verny, C, Durosier, G, Birouk, N, Gouider, R, Salih, M, Bouhouche, A, Thiam, A, Grid, D, Mayer, M, Ruberg, M, Tazir, M, Brice, A, LeGuern, E

“…Autosomal-recessive forms of Charcot-Marie-Tooth (ARCMT) account for less than 10% of the families in the European CMT population but are more frequent in the…”
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Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C by Tazir, M., Azzedine, H., Assami, S., Sindou, P., Nouioua, S., Zemmouri, R., Hamadouche, T., Chaouch, M., Feingold, J., Vallat, J. M., Leguern, E., Grid, D.

“…Autosomal recessive forms of axonal Charcot–Marie–Tooth (ARCMT2) disease are frequent in some areas, such as North Africa and the Middle East, since…”
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Low disease risk in relatives of north african lrrk2 Parkinson disease patients by Troiano, A R, Elbaz, A, Lohmann, E, Belarbi, S, Vidailhet, M, Bonnet, A-M, Lesage, S, Pollak, P, Cazeneuve, C, Borg, M, Feingold, J, Dürr, A, Tazir, M, Brice, A

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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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P070 IL-17 and nitric oxide pathways are involved in inflammatory response during Alzheimer’s disease: A study in Algerian patients by Belkhelfa, M., Rafa, H., Medjeber, O., Behairi, N., Abada-Bendib, M., Makrelouf, M., Belarbi, S., Masmoudi, A.N., Tazir, M., Touil-Boukoffa, C.

“…Alzheimer’s disease (AD) is a neurodegenerative disorder leading to cognitive impairment (amnesia, aphasia, apraxia and agnosia), characterized by three major…”
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