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stephane Blanche
stephane Blanche
professeur de pediatrie , Paris
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Year
Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1
S Hacein-Bey-Abina, A Garrigue, GP Wang, J Soulier, A Lim, E Morillon, ...
The Journal of clinical investigation 118 (9), 3132-3142, 2008
21672008
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), 818-823, 2009
17412009
Interferon-γ–receptor deficiency in an infant with fatal bacille Calmette–Guérin infection
E Jouanguy, F Altare, S Lamhamedi, P Revy, JF Emile, M Newport, ...
New England Journal of Medicine 335 (26), 1956-1962, 1996
11261996
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3)
J Feldmann, I Callebaut, G Raposo, S Certain, D Bacq, C Dumont, ...
Cell 115 (4), 461-473, 2003
10692003
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
R Döffinger, A Smahi, C Bessia, F Geissmann, J Feinberg, A Durandy, ...
Nature genetics 27 (3), 277-285, 2001
9432001
Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
L Liu, S Okada, XF Kong, AY Kreins, S Cypowyj, A Abhyankar, J Toubiana, ...
Journal of Experimental Medicine 208 (8), 1635-1648, 2011
8832011
Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
A Puel, R Döffinger, A Natividad, M Chrabieh, G Barcenas-Morales, ...
Journal of Experimental Medicine 207 (2), 291-297, 2010
8122010
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues
S Blanche, M Tardieu, P Rustin, A Slama, B Barret, G Firtion, ...
The Lancet 354 (9184), 1084-1089, 1999
7941999
Efficacy of gene therapy for X-linked severe combined immunodeficiency
S Hacein-Bey-Abina, J Hauer, A Lim, C Picard, GP Wang, CC Berry, ...
New England Journal of Medicine 363 (4), 355-364, 2010
7622010
Gene therapy in a patient with sickle cell disease
JA Ribeil, S Hacein-Bey-Abina, E Payen, A Magnani, M Semeraro, ...
New England Journal of Medicine 376 (9), 848-855, 2017
7482017
A prospective study of infants born to women seropositive for human immunodeficiency virus type 1
S Blanche, C Rouzioux, MLG Moscato, F Veber, MJ Mayaux, C Jacomet, ...
New England Journal of Medicine 320 (25), 1643-1648, 1989
7251989
Gene therapy in patients with transfusion-dependent β-thalassemia
AA Thompson, MC Walters, J Kwiatkowski, JEJ Rasko, JA Ribeil, ...
New England Journal of Medicine 378 (16), 1479-1493, 2018
7032018
Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99
C Antoine, S Müller, A Cant, M Cavazzana-Calvo, P Veys, J Vossen, ...
The Lancet 361 (9357), 553-560, 2003
6322003
Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte Society.
M Arico, G Janka, A Fischer, JI Henter, S Blanche, G Elinder, M Martinetti, ...
Leukemia 10 (2), 197-203, 1996
5801996
Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.
A Rötig, V Cormier, S Blanche, JP Bonnefont, F Ledeist, N Romero, ...
The Journal of clinical investigation 86 (5), 1601-1608, 1990
5441990
Lamivudine-zidovudine combination for prevention of maternal-infant transmission of HIV-1
L Mandelbrot, A Landreau-Mascaro, C Rekacewicz, A Berrebi, JL Bénifla, ...
Jama 285 (16), 2083-2093, 2001
5122001
Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations
N Jeremiah, B Neven, M Gentili, I Callebaut, S Maschalidi, ...
The Journal of clinical investigation 124 (12), 5516-5520, 2014
5062014
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
J Toubiana, S Okada, J Hiller, M Oleastro, M Lagos Gomez, ...
Blood, The Journal of the American Society of Hematology 127 (25), 3154-3164, 2016
4962016
Partial interferon-gamma receptor 1 deficiency in a child with tuberculoid bacillus Calmette-Guérin infection and a sibling with clinical tuberculosis.
E Jouanguy, S Lamhamedi-Cherradi, F Altare, MC Fondanèche, ...
The Journal of clinical investigation 100 (11), 2658-2664, 1997
4801997
A modified γ-retrovirus vector for X-linked severe combined immunodeficiency
S Hacein-Bey-Abina, SY Pai, HB Gaspar, M Armant, CC Berry, S Blanche, ...
New England Journal of Medicine 371 (15), 1407-1417, 2014
4622014
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