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51

Mutation in RAP1 is a rare event in myelodysplastic syndromes

Gyan, E, Frew, M, Bowen, D, Beldjord, C, Preudhomme, C, Lacombe, C, Mayeux, P, Dreyfus, F, Porteu, F, Fontenay, M

Journal:

Year:

2005

Language:

english

File:

PDF, 196 KB

english, 2005

52

IgH/TCR rearrangements are common in MLL translocated adult AML and suggest an early T/myeloid or B/myeloid maturation arrest, which correlates with the MLL partner

Dupret, C, Asnafi, V, Leboeuf, D, Millien, C, Ben Abdelali, R, Preudhomme, C, Beldjord, K, Delabesse, E, Macintyre, E

Journal:

Year:

2005

Language:

english

File:

PDF, 76 KB

english, 2005

53

HOXA cluster deregulation in T-ALL associated with both a TCRD-HOXA and a CALM-AF10 chromosomal translocation

Bergeron, J, Clappier, E, Cauwelier, B, Dastugue, N, Millien, C, Delabesse, E, Beldjord, K, Speleman, F, Soulier, J, Macintyre, E

Journal:

Year:

2006

Language:

english

File:

PDF, 220 KB

english, 2006

54

Deletion of filamin A in two female patients with periventricular nodular heterotopia

Jodi Warman Chardon, Cyril Mignot, Swaroop Aradhya, Boris Keren, Alexandra Afenjar, Anna Kaminska, Cherif Beldjord, Delphine Héron, Kym M. Boycott

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 259 KB

english, 2012

55

Human T-Lymphoid Progenitors Generated in a Feeder-Cell-Free Delta-Like-4 Culture System Promote T-Cell Reconstitution in NOD/SCID/γc−/− Mice

Christian Reimann, Emmanuelle Six, Liliane Dal-Cortivo, Andrea Schiavo, Kevin Appourchaux, Chantal Lagresle-Peyrou, Corinne de Chappedelaine, Brigitte Ternaux, Laure Coulombel, Kheira Beldjord, Marina

Journal:

Year:

2012

Language:

english

File:

PDF, 461 KB

english, 2012

56

Coexistence of LMPP-like and GMP-like Leukemia Stem Cells in Acute Myeloid Leukemia

Nicolas Goardon, Emanuele Marchi, Ann Atzberger, Lynn Quek, Anna Schuh, Shamit Soneji, Petter Woll, Adam Mead, Kate A. Alford, Raj Rout, Salma Chaudhury, Amanda Gilkes, Steve Knapper, Kheira Beldjord,

Journal:

Year:

2011

Language:

english

File:

PDF, 1.84 MB

english, 2011

57

Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation

Pierre Billuart, Jamel Chelly, Alain Carrié, Marie-Claude Vinet, Philippe Couvert, Nathalie McDonell, Ramzi Zemni, Axel Kahn, Claude Moraine, Cherif Beldjord, Thierry Bienvenu

Journal:

Annales de Génétique

Year:

2000

Language:

english

File:

PDF, 58 KB

english, 2000

58

Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies

A. Elbaz, J. Suédois, M. Duquesnoy, C. Beldjord, C. Berchel, G. Mérault

Journal:

Journal of Intellectual Disability Research

Year:

1998

Language:

english

File:

PDF, 289 KB

english, 1998

59

RAPID DETECTION OF A MEDITERRANEAN β° SPLICE JUNCTION MUTATION BY DNA AMPLIFICATION AND BsaB1 MAPPING

C. Bennani, P. Sebillon, R. Krishnamoorthy, D. Labie, C. Beldjord

Journal:

British Journal of Haematology

Year:

1990

Language:

english

File:

PDF, 291 KB

english, 1990

60

The spectrum of β-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy

C. Bennani, R. Tamouza, F. Rouabhi, M. Benabadji, M. Malou, J. Elion, D. Labie, C. Beldjord

Journal:

British Journal of Haematology

Year:

1993

Language:

english

File:

PDF, 268 KB

english, 1993

61

Cloning and characterization of the human V3 pituitary vasopressin receptor

Yves de Keyzer, Colette Auzan, Frédéric Lenne, Chérif Beldjord, Marc Thibonnier, Xavier Bertagna, Eric Clauser

Journal:

Year:

1994

Language:

english

File:

PDF, 707 KB

english, 1994

62

Consistency of routine measurements of CD4+, CD8+ peripheral blood lymphocytes

J.P. Aboulker, B. Autran, K. Beldjord, F. Touraine, P. Debre

Journal:

Journal of Immunological Methods

Year:

1992

Language:

english

File:

PDF, 403 KB

english, 1992

63

Hétérogénéité génétique des retards mentaux non spécifiques liés au chromosome X: étude clinique et génétique de deux familles

V. des Portes, N. Soufir, L. Bachner, C. Beldjord, P. Billuart, T. Bienvenu, M.C. Vinet, T. Brüls, L. Telvi, G. Ponsot, J. Boué, J. Chelly

Journal:

Archives de Pédiatrie

Year:

1996

File:

PDF, 148 KB

1996

64

Localisation en Xp22.33-pter d'un syndrome neurodégénératif familial récessif lié au chromosome X, caractérisé par une ataxie congénitale, une épilepsie myoclonique progressive et une rétinopathie maculaire

V. des Portes, P. Billuart, T. Bienvenu, L. Bachner, C. Beldjord, N. Soufir, M.C. Vinet, T. Brüls, E. Malaspina, V. Marchiani, E. Bertini, A. Kahn, E. Franzoni, J. Chelly

Journal:

Archives de Pédiatrie

Year:

1996

File:

PDF, 141 KB

1996

65

804 Epstein-Barr virus and Hodgkin's disease: Comparison between Algerian and French patients

F. Zerhouni, M.I. Belkaïd, K. Beldjord, J. Brière, M. Andrieu, P. Colonna

Journal:

European Journal of Cancer

Year:

1995

Language:

english

File:

PDF, 165 KB

english, 1995

66

Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan)

J.-C. Kaplan, F. Piccolo, K. Azibi, A. Carrié, F. Leturcq, C. de Toma, C. Beldjord, M. Chaouch, A. Sefiani, L. Merlini, T. Voit, C. Sewry, Y. Sunada, J.S. Beckmann, N. Rornero, F.M.S. Tomé, M. Fardeau

Journal:

Neuromuscular Disorders

Year:

1996

Language:

english

File:

PDF, 101 KB

english, 1996

67

Cytokines and culture medium have a major impact on human in vitro T-cell differentiation

Emmanuelle M. Six, Fatine Benjelloun, Alexandrine Garrigue, Delphine Bonhomme, Estelle Morillon, Julien Rouiller, Laure Cacavelli, Johanna Blondeau, Kheira Beldjord, Salima Hacein-Bey-Abina, Marina Ca

Journal:

Blood Cells, Molecules, and Diseases

Year:

2011

Language:

english

File:

PDF, 1.06 MB

english, 2011

68

Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons

Karine Poirier, Hilde Van Esch, Gaëlle Friocourt, Yoann Saillour, Nadia Bahi, Stéphanie Backer, Evelyne Souil, Laetitia Castelnau-Ptakhine, Cherif Beldjord, Fiona Francis, Thierry Bienvenu, Jamel Chel

Journal:

Molecular Brain Research

Year:

2004

Language:

english

File:

PDF, 1.01 MB

english, 2004

69

Detection of polymorphism in the Trypanosoma cruzi TcP2β gene family by single strand conformational analysis (SSCA)

Martín P. Vázquez, Cherif Beldjord, Hernán Lorenzi, Thierry Bienvenu, Mariano J. Levin

Journal:

Year:

1996

Language:

english

File:

PDF, 621 KB

english, 1996

70

Retard mental et troubles de la corticogenèse

V. Des Portes, J.M. Pinard, F. Francis, C. Beldjord, G. Ponsot, J. Chelly

Journal:

Archives de Pédiatrie

Year:

2000

File:

PDF, 300 KB

2000

71

Identification du gène XLIS, codant pour la doublecortine et impliqué dans les hétérotopies laminaires sous-corticales et les lissencéphalies liées à l'X

V Des Portes, JM Pinard, F Francis, MC Vinet, A Koulakoff, J Motte, M Catala, C Beldjord, J Chelly

Journal:

Archives de Pédiatrie

Year:

1998

Language:

french

File:

PDF, 323 KB

french, 1998

72

Implication du gène Rab-GDI (Rab gdp-dissociation-inhibitor) dans deux familles atteintes de retard mental non spécifique lié au chromosome X

A de Saint Martin, V des Portes, T Bienvenu, A Danion, M Fischbach, C Beldjord, J Chelly

Journal:

Archives de Pédiatrie

Year:

1998

File:

PDF, 146 KB

1998

73

Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene

Christophe Béroud, Alain Carrié, Chérif Beldjord, Nathalie Deburgrave, Stéphane Llense, Nadège Carelle, Cécile Peccate, Jean-Marie Cuisset, Florence Pandit, Frédérique Carré-Pigeon, Michèle Mayer, Rém

Journal:

Neuromuscular Disorders

Year:

2004

Language:

english

File:

PDF, 301 KB

english, 2004

74

From adhalinopathies to alpha-sarcoglycanopathies: An overview

M. Jeanpierre, A. Carrié, F. Piccolo, F. Leturcq, K. Azibi, C. De Toma, C. Beldjord, L. Merlini, T. Voit, N. Romero, Y. Sunada, F.M.S. Tomé, M. Fardeau, K.P. Campbell, J.-C. Kaplan

Journal:

Neuromuscular Disorders

Year:

1996

Language:

english

File:

PDF, 273 KB

english, 1996

75

Genetic and allelic heterogeneity of LGMD in North Africa

K. Azibi, M. Chaouch, A. Reghis, F. El Kerch, A. Sbiti, A. Sefiani, F. Leturcq, M. Jeanpierre, A. Carrié, F. Piccolo, C. Beldjord, J.-C. Kaplan

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 128 KB

english, 1997

76

Flow cytometry and IG/TCR quantitative PCR for minimal residual disease quantitation in acute lymphoblastic leukemia: a French multicenter prospective study on behalf of the FRALLE, EORTC and GRAALL

Garand, R, Beldjord, K, Cavé, H, Fossat, C, Arnoux, I, Asnafi, V, Bertrand, Y, Boulland, M-L, Brouzes, C, Clappier, E, Delabesse, E, Fest, T, Garnache-Ottou, F, Huguet, F, Jacob, M-C, Kuhlein, E, Mart

Journal:

Year:

2013

Language:

english

File:

PDF, 528 KB

english, 2013

77

Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia

Zanni, G., Saillour, Y., Nagara, M., Billuart, P., Castelnau, L., Moraine, C., Faivre, L., Bertini, E., Durr, A., Guichet, A., Rodriguez, D., des Portes, V., Beldjord, C., Chelly, J.

Journal:

Year:

2005

Language:

english

File:

PDF, 759 KB

english, 2005

78

Effects of cyclosporin on T-cell subsets in human immunodeficiency virus disease

Jean-Marie Andrieu, Philippe Even, Alain Venet, Jean-Marc Tourani, Marc Stern, William Lowenstein, Christine Audroin, Denise Eme, Dominique Masson, Herve Sors, Dominique Israel-Biet, Kheira Beldjord

Journal:

Clinical Immunology and Immunopathology

Year:

1988

Language:

english

File:

PDF, 1.10 MB

english, 1988

79

Budd-Chiari syndrome and factor V Leiden mutation

M-H. Denninger, K. Beldjord, F. Durand, C. Denie, D. Valla, M-C. Guillin, A.E.A. Mahmoud, J.T. Wilde, E. Elias

Journal:

Year:

1995

Language:

english

File:

PDF, 332 KB

english, 1995

80

Detection of parasite DNA in Chagas' heart disease

Silvia Brandariz, Alejandro Schijman, Carlos Vigliano, Pablo Arteman, Rodolfo Viotti, Cherif Beldjord, Mariano Jorge Levin

Journal:

Year:

1995

Language:

english

File:

PDF, 443 KB

english, 1995

81

LHX2 deregulation by juxtaposition with the IGH locus in a pediatric case of chronic myeloid leukemia in B-cell lymphoid blast crisis

Nathalie Nadal, Elise Chapiro, Pascale Flandrin-Gresta, Sandrine Thouvenin, Christian Vasselon, Kheira Beldjord, Odile Fenneteau, Olivier Bernard, Lydia Campos, Florence Nguyen-Khac

Journal:

Leukemia Research

Year:

2012

Language:

english

File:

PDF, 451 KB

english, 2012

82

A novel, rapid, and accurate method for detecting microdeletion involving the DAZ gene in infertile men

Hervé Lucas, Catherine Patrat, Pierre Jouannet, Cherif Beldjord, Thierry Bienvenu

Journal:

Fertility and Sterility

Year:

2000

Language:

english

File:

PDF, 286 KB

english, 2000

83

So-called ‘cryptogenic’ partial seizures resulting from a subtle cortical dysgenesis due to adoublecortin gene mutation

V.des Portes, I Souville, F Francis, J.M Pinard, J Chelly, C Beldjord, P.S Jouk, L Abaoub, A Joannard

Journal:

Year:

2002

Language:

english

File:

PDF, 396 KB

english, 2002

84

β-Thalassemia in Algeria

D. LABIE, C. BENNANI, C. BELDJORD

Journal:

Annals of the New York Academy of Sciences

Year:

1990

Language:

english

File:

PDF, 727 KB

english, 1990

85

Toward a NOTCH1/FBXW7/RAS/PTEN-Based Oncogenetic Risk Classification of Adult T-Cell Acute Lymphoblastic Leukemia: A Group for Research in Adult Acute Lymphoblastic Leukemia Study

Trinquand, A., Tanguy-Schmidt, A., Ben Abdelali, R., Lambert, J., Beldjord, K., Lengline, E., De Gunzburg, N., Payet-Bornet, D., Lhermitte, L., Mossafa, H., Lheritier, V., Bond, J., Huguet, F., Buzyn,

Journal:

Journal of Clinical Oncology

Year:

2013

Language:

english

File:

PDF, 338 KB

english, 2013

86

Novel activating JAK2 mutation in a patient with Down syndrome and B-cell precursor acute lymphoblastic leukemia

Malinge, S., Ben-Abdelali, R., Settegrana, C., Radford-Weiss, I., Debre, M., Beldjord, K., Macintyre, E. A., Villeval, J.-L., Vainchenker, W., Berger, R., Bernard, O. A., Delabesse, E., Penard-Lacroni

Journal:

Year:

2007

Language:

english

File:

PDF, 219 KB

english, 2007

87

Oncogenetics and minimal residual disease are independent outcome predictors in adult patients with acute lymphoblastic leukemia

Beldjord, K., Chevret, S., Asnafi, V., Huguet, F., Boulland, M.-L., Leguay, T., Thomas, X., Cayuela, J.-M., Grardel, N., Chalandon, Y., Boissel, N., Schaefer, B., Delabesse, E., Cave, H., Chevallier,

Journal:

Year:

2014

Language:

english

File:

PDF, 941 KB

english, 2014

88

The wide spectrum of tubulinopathies: what are the key features for the diagnosis?

Bahi-Buisson, N., Poirier, K., Fourniol, F., Saillour, Y., Valence, S., Lebrun, N., Hully, M., Fallet Bianco, C., Boddaert, N., Elie, C., Lascelles, K., Souville, I., Beldjord, C., Chelly, J.

Journal:

Year:

2014

Language:

english

File:

PDF, 1.80 MB

english, 2014

89

Éfficacité et tolérance de l’alemtuzumab dans les lymphomes T épidermotropes de stade avancé : étude rétrospective de 39 cas en pratique clinique

De Masson, A., Guitera, P., Michel, L., Bouaziz, J.-D., Brice, P., Moulonguet, I., Mouly, F., Roux, J., Ram-Wolff, C., Beldjord, K., Cayuela, J.-M., Bachelez, H., Bensussan, A., Bagot, M.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2013

Language:

french

File:

PDF, 64 KB

french, 2013

90

Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1

Wahbi, Karim, Algalarrondo, Vincent, Bécane, Henri Marc, Fressart, Véronique, Beldjord, Chérif, Azibi, Kamel, Lazarus, Arnaud, Berber, Nawal, Radvanyi-Hoffman, Hélène, Stojkovic, Tanya, Béhin, Anthony

Journal:

Archives of Cardiovascular Diseases

Year:

2013

File:

PDF, 1.64 MB

2013

91

Lissencéphalies : étude moléculaire de deux familles algériennes

Boudrahem Addour, Nassima, Mekki, Azzedine, Makri, Salima, Benhassine, Traki, Beldjord, Cherif

Journal:

Revue Neurologique

Year:

2012

Language:

french

File:

PDF, 68 KB

french, 2012

92

Exploration moléculaire des lissencéphalies : à propos de quatre cas

Boudrahem-Addour, N., Carion, N., Moualek, D., Mekki, A., Benhassine, T., Beldjord, C.

Journal:

Revue Neurologique

Year:

2014

Language:

french

File:

PDF, 261 KB

french, 2014

93

[Part 1: Biological Sciences] || Evidence for the Multicentric Origin of the Sickle Cell Hemoglobin Gene in Africa

Josee Pagnier, J. Gregory Mears, Olga Dunda-Belkhodja, Kim E. Schaefer-Rego, Cherif Beldjord, Ronald L. Nagel and Dominque Labie

Journal:

Proceedings of the National Academy of Sciences

Year:

1984

Language:

english

File:

PDF, 595 KB

english, 1984

94

Somatic Mutations of the β -catenin Gene are Frequent in Mouse and Human Hepatocellular Carcinomas

Alix De La Coste, Beatrice Romagnolo, Pierre Billuart, Claire-Angelique Renard, Marie-Annick Buendia, Olivier Soubrane, Monique Fabre, Jamel Chelly, Cherif Beldjord, Axel Kahn and Christine Perret

Journal:

Proceedings of the National Academy of Sciences

Year:

1998

Language:

english

File:

PDF, 1.34 MB

english, 1998

95

Anthropological Approach to the Heterogeneity of ß-Thalassemia Mutations in Northern Africa

C. BENNANI, R. BOUHASS, P. PERRIN-PECONTAL, R. TAMOUZA, M. MALOU, J. ELION, G. TRABUCHET, C. BELDJORD, M. BENABADJI and D. LABIE

Journal:

Year:

1994

Language:

english

File:

PDF, 1.13 MB

english, 1994

96

Rapid and Direct Detection of the Most Frequent Mediterranean β-Thalassemic Mutations by Multiplex Allele-Specific Enzymatic Amplification

THIERRY BIENVENU, PASCALE SEBILLON, DOMINIQUE LABIE, JEAN CLAUDE KAPLAN and CHERIF BELDJORD

Journal:

Year:

1992

Language:

english

File:

PDF, 763 KB

english, 1992

97

Malformations cérébrales et épilepsie : présentations radiocliniques et implications pour le diagnostic génétique

Bahi-Buisson, N., Boddaert, N., Saillour, Y., Souville, I., Poirier, K., Léger, P.-L., Castelnau, L., Plouin, P., Carion, N., Beldjord, C., Chelly, J.

Journal:

Revue Neurologique

Year:

2008

File:

PDF, 3.72 MB

2008

98

Detection of Two Rare β-Thalassemia Alleles Found in the Tunisian Population: Codon 47 (+A) and Codons 106/107 (+G)

Bibi, Amina, Messaoud, Taieb, Beldjord, Cherif, Fattoum, Slaheddine

Journal:

Year:

2006

Language:

english

File:

PDF, 151 KB

english, 2006

99

CD158k Is a Reliable Marker for Diagnosis of Sézary Syndrome and Reveals an Unprecedented Heterogeneity of Circulating Malignant Cells

Moins-Teisserenc, Hélène, Daubord, Magali, Clave, Emmanuel, Douay, Corinne, Félix, Joana, Marie-Cardine, Anne, Ram-Wolff, Caroline, Maki, Guitta, Beldjord, Kheira, Homyrda, Laurence, Michel, Laurence,

Journal:

The Journal of Investigative Dermatology

Year:

2015

Language:

english

File:

PDF, 1.44 MB

english, 2015

100

Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem

Boudrahem-Addour, Nassima, Zidani, Nadia, Carion, Nathalie, Labie, Dominique, Belhani, Meriem, Beldjord, Cherif

Journal:

Year:

2009

Language:

english

File:

PDF, 178 KB

english, 2009