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1

Troubles cognitifs dans le Neuro-Behcet : étude cas témoins

Mostefaoui, Farida, Belarbi, Soreya, Kediha, Mohamed Islam, Smail, Nourredine, Tazir, Meriem

Journal:

Revue Neurologique

Year:

2017

Language:

french

File:

PDF, 65 KB

french, 2017

2

The classification of Charcot-Marie-Tooth diseases, a never-ending story: CMT4?

Vallat, Jean-Michel, Tazir, Meriem, Magy, Laurent, Le Masson, Gwendal, Mathis, Stéphane

Journal:

Year:

2018

Language:

english

File:

PDF, 238 KB

english, 2018

3

L’ataxie avec déficit en vitamine E (AVED). Diagnostic moléculaire dans une vingtaine de familles algériennes

Benhassine, Traki, Ferrat, Farida, Ali Pacha, Lamia, Chaouch, Malika, Tazir, Meriem, Hamadouche, Tarik

Journal:

Revue Neurologique

Year:

2012

Language:

french

File:

PDF, 78 KB

french, 2012

4

Diagnostic génétique de la forme PARK8 de la maladie de Parkinson en Algérie par recherche de la mutation c 6055G>A (p gly2019ser) dans le gène LRRK2

Hamadouche, T., Belarbi, S., Hecham, N., Lesage, S., Brice, A., Tazir, M., Benhassine, T.

Journal:

Revue Neurologique

Year:

2013

Language:

french

File:

PDF, 195 KB

french, 2013

5

Encéphalites autoimmunes à autoanticorps : diversité clinique et immunologique

Bakhti, Tahar Amine, Nouioua, Sonia, Attal, Nabila, Bouderba, Radia, Pacha, Lamia Ali, Assami, Salima, Tazir, Meriem

Journal:

Revue Neurologique

Year:

2017

Language:

french

File:

PDF, 64 KB

french, 2017

6

Neuropathies périphériques héréditaires

Jean-Michel Vallat, Mériem Tazir, Judith Calvo, Benoît Funalot

Journal:

La Presse Médicale

Year:

2009

File:

PDF, 167 KB

2009

7

Prevalence and characterization of extended-spectrum β-lactamases in Klebsiella pneumoniae in Algiers hospitals (Algeria)

Y. Messai, H. Iabadene, T. Benhassine, S. Alouache, M. Tazir, V. Gautier, G. Arlet, R. Bakour

Journal:

Pathologie Biologie

Year:

2008

File:

PDF, 158 KB

2008

8

Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update

Tazir, Meriem, Hamadouche, Tarik, Nouioua, Sonia, Mathis, Stephane, Vallat, Jean-Michel

Journal:

Journal of the Neurological Sciences

Year:

2014

Language:

english

File:

PDF, 1.03 MB

english, 2014

9

[IEEE 2015 International Conference on Advanced Robotics (ICAR) - Istanbul, Turkey (2015.7.27-2015.7.31)] 2015 International Conference on Advanced Robotics (ICAR) - Mobile robot path planning for complex dynamic environments

Tazir, Mohamed Lamine, Azouaoui, Ouahiba, Hazerchi, Mohamed, Brahimi, Mohamed

Year:

2015

Language:

english

File:

PDF, 665 KB

english, 2015

10

CICP: Cluster Iterative Closest Point for sparse-dense point cloud registration

Tazir, Mohammed Lamine, Gokhool, Tawsif, Checchin, Paul, Malaterre, Laurent, Trassoudaine, Laurent

Journal:

Robotics and Autonomous Systems

Year:

2018

Language:

english

File:

PDF, 7.58 MB

english, 2018

11

Serotypes and Antibiotic Susceptibility of Streptococcus pneumoniae Isolates from Invasive Pneumococcal Disease and Asymptomatic Carriage in a Pre-vaccination Period, in Algeria

Ziane, Hanifa, Manageiro, Vera, Ferreira, Eugénia, Moura, Inês B., Bektache, Soumia, Tazir, Mohamed, Caniça, Manuela

Journal:

Frontiers in Microbiology

Year:

2016

Language:

english

File:

PDF, 2.46 MB

english, 2016

12

Facilitators to Accessibility of HIV/AIDS-Related Health Services among Transgender Women Living with HIV in Yogyakarta, Indonesia

Fauk, Nelsensius Klau, Merry, Maria Silvia, Siri, Theodorus Asa, Tazir, Fabiola Tazrina, Sigilipoe, Mitra Andhini, Tarigan, Kristin Oktanita, Mwanri, Lillian

Journal:

AIDS Research and Treatment

Year:

2019

Language:

english

File:

PDF, 1.52 MB

english, 2019

13

Survival probabilities of stomach and colon cancer patients in Bangladesh

Ahammed, Tanvir, Akter, Mst Farzana, Suchana, Afroza Jannat, Chowdhury, Anisa Ahmed, Shah, Md Rafil Tazir, Rahman, Md Siddkur, Akter, Ayesha, Ullah, Mohammad Ohid

Journal:

Asian Journal of Medical and Biological Research

Year:

2020

File:

PDF, 254 KB

2020

14

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

Suzanne Lesage, Pablo Ibanez, Ebba Lohmann, Pierre Pollak, François Tison, Myriem Tazir, Anne-Louise Leutenegger, Joao Guimaraes, Anne-Marie Bonnet, Yves Agid, Alexandra Dürr, Alexis Brice

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 79 KB

english, 2005

15

Identification of seven novel mutations in the GAN gene

P. Bomont, C. Ioos, C. Yalcinkaya, R. Korinthenberg, JM. Vallat, S. Assami, A. Munnich, B. Chabrol, G. Kurlemann, M. Tazir, M. Koenig

Journal:

Year:

2003

Language:

english

File:

PDF, 31 KB

english, 2003

16

Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations

Salima Assami, Hamid Azzedine, Sonia Nouioua, Emeline Mundwiller, Soulaiman Mahoui, Samira Makri, Meriam Djemai, Djamel Grid, Alexis Brice, Tarik Hamadouche, Giovanni Stevanin, Meriem Tazir

Journal:

Movement Disorders

Year:

2011

Language:

english

File:

PDF, 486 KB

english, 2011

17

Homozygous Defects In Lmna, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy In Human (Charcot-Marie-Tooth Disorder Type 2) And Mouse

A De Sandre-Giovannoli, M Chaouch, S Kozlov, JM Vallat, M Tazir, N Kassouri, P Szepetowski, T Hammadouche, A Vandenberghe, CL Stewart, D Grid, N. Levy

Journal:

Journal of the Peripheral Nervous System

Year:

2002

Language:

english

File:

PDF, 74 KB

english, 2002

18

Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance

Jean-Michel Vallat, Laurent Magy, Emmeline Lagrange, Franck Sturtz, Corinne Magdelaine, Djamel Grid, Mériem Tazir

Journal:

Acta Neuropathologica

Year:

2007

Language:

english

File:

PDF, 552 KB

english, 2007

19

Refinement of theSPG15candidate interval and phenotypic heterogeneity in three large Arab families

Nizar Elleuch, Naima Bouslam, Sylvain Hanein, Alexander Lossos, Abdelmadjid Hamri, Stephan Klebe, Vardiella Meiner, Nezha Birouk, Israela Lerer, Djamel Grid, Delphine Bacq, Meriem Tazir, Diana Zelenik

Journal:

Year:

2007

Language:

english

File:

PDF, 223 KB

english, 2007

20

Autosomal recessive forms of Charcot-Marie-Tooth disease

J. M. Vallat, D. Grid, C. Magdelaine, F. Sturtz, M. Tazir

Journal:

Current Neurology and Neuroscience Reports

Year:

2004

Language:

english

File:

PDF, 343 KB

english, 2004

21

High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in Algiers

K. Antri, N. Rouzic, O. Dauwalder, I. Boubekri, M. Bes, G. Lina, F. Vandenesch, M. Tazir, N. Ramdani-Bouguessa, J. Etienne

Journal:

Clinical Microbiology and Infection

Year:

2011

Language:

english

File:

PDF, 115 KB

english, 2011

22

Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot-Marie-Tooth Subtype CMT2B1 in Families from North Western Africa

T. Hamadouche, Y. Poitelon, E. Genin, M. Chaouch, M. Tazir, N. Kassouri, S. Nouioua, A. Chaouch, I. Boccaccio, T. Benhassine, A. De Sandre-Giovannoli, D. Grid, N. Lévy, V. Delague

Journal:

Annals of Human Genetics

Year:

2008

Language:

english

File:

PDF, 487 KB

english, 2008

23

10.1038/81701

Koenig, Michel, Bomont, Pascale, Cavalier, Laurent, Blondeau, François, Hamida, Christiane Ben, Belal, Samir, Tazir, Meriem, Demir, Ercan, Topaloglu, Haluk, Korinthenberg, Rudolf, Tüysüz, Beyhan, Land

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 290 KB

english, 2000

24

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

Tranchant, Christine, Aubourg, Patrick, Tazir, Meriem, Schöls, Lüdger, Moreira, Maria-Céu, Klur, Sandra, Watanabe, Mitsunori, Németh, Andrea H, Ber, Isabelle Le, Moniz, José-Carlos

Journal:

Nature Genetics

Year:

2004

Language:

english

File:

PDF, 158 KB

english, 2004

25

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

O. Dubourg, H. Azzedine, C. Verny, G. Durosier, N. Birouk, R. Gouider, M. Salih, A. Bouhouche, A. Thiam, D. Grid, M. Mayer, M. Ruberg, M. Tazir, A. Brice, E. LeGuern

Journal:

NeuroMolecular Medicine

Year:

2006

Language:

english

File:

PDF, 166 KB

english, 2006

26

Evaluation of the chloride and bromide salts of cetylpyridium for the transportation of sputum in tuberculosis bacteriology

M. Tazir, Hugo L. David, Fadila Boulahbal

Journal:

Year:

1979

Language:

english

File:

PDF, 387 KB

english, 1979

27

ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency

Clotilde Lagier-Tourenne, Meriem Tazir, Luis Carlos López, Catarina M. Quinzii, Mirna Assoum, Nathalie Drouot, Cleverson Busso, Samira Makri, Lamia Ali-Pacha, Traki Benhassine, Mathieu Anheim, David R

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 1.74 MB

english, 2008

28

Molecular and functional characterisation of the heat shock protein 10 of Strongyloides ratti

Yasmina Tazir, Vera Steisslinger, Hanns Soblik, Abuelhassan Elshazly Younis, Svenja Beckmann, Christoph G. Grevelding, Hanno Steen, Norbert W. Brattig, Klaus D. Erttmann

Journal:

Molecular and Biochemical Parasitology

Year:

2009

Language:

english

File:

PDF, 772 KB

english, 2009

29

Use of two methods of analysis to estimate the annual rate of tuberculosis infection in Southern Algeria

R. Liard, M. Tazir, F. Boulahba, S. Perdrizet

Journal:

Tubercle and Lung Disease

Year:

1996

Language:

english

File:

PDF, 846 KB

english, 1996

30

P070 IL-17 and nitric oxide pathways are involved in inflammatory response during Alzheimer’s disease: A study in Algerian patients

M. Belkhelfa, H. Rafa, O. Medjeber, N. Behairi, M. Abada-Bendib, M. Makrelouf, S. Belarbi, A.N. Masmoudi, M. Tazir, C. Touil-Boukoffa

Journal:

Year:

2012

Language:

english

File:

PDF, 133 KB

english, 2012

31

P.P.1 03 A clinical, morphological and genetic study of congenital muscular dystrophies in Algeria

S. Makri, N. Terki, S. Belarbi, S. Assami, S. Maugenre, C. Gartioux, V. Allamand, P. Richard, N.B. Romero, M. Ait Kaci-Ahmed, D. Grid, P. Guicheney, M. Tazir

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 61 KB

english, 2006

32

G.P.4.02 Pathophysiological mechanisms of lamin A/C associated Charcot-Marie-Tooth disease (CMT2B1/ARCMT2)

Y. Poitelon, T. Hamadouche, A. De Sandre-Giovannoli, S. Kozlov, N. Serradj, M. Tazir, M. Chaouch, D. Grid, C. Stewart, M. Jamon, V. Delague, N. Lévy

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 46 KB

english, 2006

33

G.P.18.01 Giant axonal neuropathy: Phenotype–genotype correlations in two cases with two novel mutations in the Gigaxonin gene

M. Tazir, K. Hühne, S. Nouioua, D. Grid, T. Hamadouche, B. Rautenstrauss, M. Vallat

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 48 KB

english, 2007

34

Phenotypic variability in giant axonal neuropathy

Meriem Tazir, Sonia Nouioua, Laurent Magy, Kathrin Huehne, Salima Assami, Andoni Urtizberea, Djamel Grid, Tarik Hamadouche, Bernd Rautenstrauss, Jean-Michel Vallat

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 443 KB

english, 2009

35

G.P.4.04 A new MTMR2 mutation is responsible for a congenital form of Charcot-Marie-Tooth disease (CMT4B1) and vocal cord paresis

M. Tazir, S. Nouioua, T. Hamadouche, R. Bernard, D. Grid, N. Levy, J.M. Vallat

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 42 KB

english, 2009

36

G.P.10.09 Description of a family associating a calpainopathy and a Duchenne myopathy

S. Nouioua, A.M. Cobo, T. Benhassine, A. Urtizberea, S. Slimani, N. Terki, S. Assami, M. Tazir

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 41 KB

english, 2009

37

G.P.10.01 DMD and SGCG molecular analysis in 200 Algerian patients affected with progressive muscular dystrophies

T. Benhassine, T. Hamadouche, K. Icheboudene, R. Drali, S. Nouioua, S. Makri, M. Chaouch, M. Tazir

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 42 KB

english, 2009

38

O.21 Genetic characterisation of PHARC – a novel syndrome resembling Refsum’s disease

L.A. Bindoff, T. Fiskerstrand, D. H’mida-Ben Brahim, S. Johansson, A. M’zahem, B.I. Haukanes, N. Drouot, J. Zimmermann, A.J. Cole, C. Vedeler, C. Bredrup, M. Assoum, M. Tazir, T. Klockgether, A. Hamri

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 36 KB

english, 2010

39

Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes

Sonia Nouioua, Tarik Hamadouche, Benoit Funalot, Rafaëlle Bernard, Nora Bellatache, Radia Bouderba, Djamel Grid, Salima Assami, Traki Benhassine, Nicolas Levy, Jean-Michel Vallat, Meriem Tazir

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 679 KB

english, 2011

40

Forte prévalence des infections communautaires et nosocomiales à Staphylococus aureus résistant à la méticilline et portant le gène de la leucocidine de Panton-Valentine dans l’Algérois

K. Antri, N. Rouzic, I. Boubekri, O. Dauwalder, A. Beloufa, H. Ziane, F. Djennane, M. Neggazi, B. Benhabyles, M. Bes, M. Tazir, J. Étienne, N. Ramdani-Bouguessa

Journal:

Pathologie Biologie

Year:

2010

File:

PDF, 244 KB

2010

41

B-11 Analyse moléculaire du caractère β-lactamase à spectre étendu des souches cliniques d'entérobactéries

S. Merabtene, T. Benhassine, M. Tazir

Journal:

Médecine et Maladies Infectieuses

Year:

2004

File:

PDF, 164 KB

2004

42

Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy

R. Zemmouri, H. Azzedine, S. Assami, N. Kitouni, J.M. Vallat, T. Maisonobe, T. Hamadouche, M. Kessaci, B. Mansouri, E. Le Guern, D. Grid, M. Tazir

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 1.65 MB

english, 2000

43

Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1

M Tazir, J.M Vallat, P Bomont, R Zemmouri, P Sindou, S Assami, S Nouioua, T Hammadouche, D Grid, M Koenig

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 199 KB

english, 2002

44

The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene

M. Chaouch, Y. Allal, A. De Sandre-Giovannoli, J.M. Vallat, A. Amer-el-Khedoud, N. Kassouri, A. Chaouch, P. Sindou, T. Hammadouche, M. Tazir, N. Lévy, D. Grid

Journal:

Neuromuscular Disorders

Year:

2003

Language:

english

File:

PDF, 176 KB

english, 2003

45

Clinical and pathological study of 80 patients with muscular dystrophy in Algeria

N. Terki, A. Masmoudi, M. Chaouch, M. Tazir, M. Ait-Kaci, D. Grid

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 262 KB

english, 1997

46

P118 Évolution de la flore microbienne et de l’antibiorésistance chez le diabétique

K. Ouerdane, S. Aouiche, M. Azzouz, R. Hannachi, A. Meftah, F. Djennane, M. Tazir, A. Boudiba

Journal:

Diabetes & Metabolism

Year:

2012

Language:

french

File:

PDF, 65 KB

french, 2012

47

Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

Annachiara De Sandre-Giovannoli, Malika Chaouch, Serguei Kozlov, Jean-Michel Vallat, Meriem Tazir, Nadia Kassouri, Pierre Szepetowski, Tarik Hammadouche, Antoon Vandenberghe, Colin L. Stewart, Djamel

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 980 KB

english, 2002

48

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

O. Dubourg, H. Azzedine, C. Verny, G. Durosier, N. Birouk, R. Gouider, M. Salih, A. Bouhouche, A. Thiam, D. Grid, M. Mayer, M. Ruberg, M. Tazir, A. Brice, E. LeGuern

Journal:

NeuroMolecular Medicine

Year:

2006

Language:

english

File:

PDF, 166 KB

english, 2006

49

Chronic childhood spinal muscular atrophies in Algeria: A genetic study

Meriem Tazir, Charles Geronimi

Journal:

Journal of the Neurological Sciences

Year:

1990

Language:

english

File:

PDF, 609 KB

english, 1990

50

A high-fat diet increases l-carnitine synthesis through a differential maturation of the Bbox1 mRNAs

Caroline Rigault, Françoise Le Borgne, Bassim Tazir, Alexandre Benani, Jean Demarquoy

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids

Year:

2013

Language:

english

File:

PDF, 857 KB

english, 2013

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