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NIZAR MAHLAOUI
NIZAR MAHLAOUI
Necker, CEREDIH, Unité ImmunoHematologie Pediatrique, Institut Imagine
Email verificata su nck.aphp.fr - Home page
Titolo
Citata da
Citata da
Anno
Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy
N Cartier, S Hacein-Bey-Abina, CC Bartholomae, G Veres, M Schmidt, ...
Science 326 (5954), 818-23, 2009
17542009
B cell–helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen
I Puga, M Cols, CM Barra, B He, L Cassis, M Gentile, L Comerma, ...
Nature immunology 13 (2), 170-180, 2012
8272012
Clinical picture and treatment of 2212 patients with common variable immunodeficiency
B Gathmann, N Mahlaoui, L Gérard, E Oksenhendler, K Warnatz, ...
Journal of Allergy and Clinical Immunology 134 (1), 116-126. e11, 2014
6262014
The European Society for Immunodeficiencies (ESID) registry working definitions for the clinical diagnosis of inborn errors of immunity
MG Seidel, G Kindle, B Gathmann, I Quinti, M Buckland, J van Montfrans, ...
The Journal of Allergy and Clinical Immunology: In Practice 7 (6), 1763-1770, 2019
4552019
Primary immunodeficiency diseases worldwide: more common than generally thought
AA Bousfiha, L Jeddane, F Ailal, I Benhsaien, N Mahlaoui, JL Casanova, ...
Journal of clinical immunology 33, 1-7, 2013
4272013
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells
M Côte, MM Ménager, A Burgess, N Mahlaoui, C Picard, C Schaffner, ...
The Journal of clinical investigation 119 (12), 3765-3773, 2009
3972009
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)
JP Schmid, D Canioni, D Moshous, F Touzot, N Mahlaoui, F Hauck, ...
Blood, The Journal of the American Society of Hematology 117 (5), 1522-1529, 2011
3802011
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
C Booth, KC Gilmour, P Veys, AR Gennery, MA Slatter, H Chapel, ...
Blood, The Journal of the American Society of Hematology 117 (1), 53-62, 2011
3482011
Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase δ …
ME Maccari, H Abolhassani, A Aghamohammadi, A Aiuti, O Aleinikova, ...
Frontiers in immunology 9, 543, 2018
3452018
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ...
Nature genetics 48 (9), 1071-1076, 2016
3432016
Coronavirus disease 2019 in patients with inborn errors of immunity: an international study
I Meyts, G Bucciol, I Quinti, B Neven, A Fischer, E Seoane, ...
Journal of Allergy and Clinical Immunology 147 (2), 520-531, 2021
3402021
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey
MO Chandesris, I Melki, A Natividad, A Puel, C Fieschi, L Yun, ...
Medicine 91 (4), e1-e19, 2012
3302012
Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an …
D Moratto, S Giliani, C Bonfim, E Mazzolari, A Fischer, HD Ochs, AJ Cant, ...
Blood, The Journal of the American Society of Hematology 118 (6), 1675-1684, 2011
3292011
Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis: a single-center report of 48 patients
M Ouachee-Chardin, C Elie, G de Saint Basile, F Le Deist, N Mahlaoui, ...
Pediatrics 117 (4), e743-e750, 2006
3252006
Evidence of innate lymphoid cell redundancy in humans
F Vély, V Barlogis, B Vallentin, B Neven, C Piperoglou, M Ebbo, T Perchet, ...
Nature immunology 17 (11), 1291-1299, 2016
3182016
Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies
A Fischer, J Provot, JP Jais, A Alcais, N Mahlaoui, D Adoue, N Aladjidi, ...
Journal of Allergy and Clinical Immunology 140 (5), 1388-1393. e8, 2017
3002017
Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: a single-center retrospective report of 38 patients
N Mahlaoui, M Ouachée-Chardin, G de Saint Basile, B Neven, C Picard, ...
Pediatrics 120 (3), e622-e628, 2007
2862007
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival
NT Nehme, JP Schmid, F Debeurme, I André-Schmutz, A Lim, P Nitschke, ...
Blood, The Journal of the American Society of Hematology 119 (15), 3458-3468, 2012
2842012
Neutrophil depletion impairs natural killer cell maturation, function, and homeostasis
BN Jaeger, J Donadieu, C Cognet, C Bernat, D Ordoñez-Rueda, ...
Journal of Experimental Medicine 209 (3), 565-580, 2012
2832012
Congenital neutropenia: diagnosis, molecular bases and patient management
J Donadieu, O Fenneteau, B Beaupain, N Mahlaoui, CB Chantelot
Orphanet journal of rare diseases 6, 1-28, 2011
2812011
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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