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au.\*:("CHAPGIER, Ariane")

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THE CLINICAL SPECTRUM OF PATIENTS WITH DEFICIENCY OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION-1AVERBUCH, Diana; CHAPGIER, Ariane; BOISSON-DUPUIS, Stéphanie et al.The Pediatric infectious disease journal. 2011, Vol 30, Num 4, pp 352-355, issn 0891-3668, 4 p.Article

BCG-osis and tuberculosis in a child with chronic granulomatous diseaseBUSTAMANTE, Jacinta; AKSU, Guzide; CASANOVA, Jean-Laurent et al.Journal of allergy and clinical immunology. 2007, Vol 120, Num 1, pp 32-38, issn 0091-6749, 7 p.Article

Disseminated Mycobacterium avium infection in a 20-year-old female with partial recessive IFNγR1 deficiencyKUMARARATNE, Dinakantha S; REMISZEWSKI, Paweł; CASANOVA, Jean-Laurent et al.Respiration (Basel). 2006, Vol 73, Num 3, issn 0025-7931, 280-282,375-378 [7 p.]Article

Impaired response to interferon-α/β and lethal viral disease in human STAT1 deficiencyDUPUIS, Stéphanie; JOUANGUY, Emmanuelle; AL GHONAIUM, Abdulaziz et al.Nature genetics. 2003, Vol 33, Num 3, pp 388-391, issn 1061-4036, 4 p.Article

Paternal Uniparental Isodisomy of Chromosome 6 Causing a Complex Syndrome Including Complete IFN-γ Receptor 1 DeficiencyPRANDO, Carolina; BOISSON-DUPUIS, Stéphanie; QIUPING ZHANG et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 3, pp 622-629, issn 1552-4825, 8 p.Article

Les mutations gain de glycosylation = Gains of glycosylation mutationsVOGT, Guillaume; CHAPGIER, Ariane; CHUZHANOVA, Nadia et al.MS. Médecine sciences. 2006, Vol 22, Num 5, pp 480-482, issn 0767-0974, 3 p.Article

Gains of glycosylation comprise an unexpectedly large group of pathogenic mutationsVOGT, Guillaume; CHAPGIER, Ariane; DE BEAUCOUDREY, Ludovic et al.Nature genetics. 2005, Vol 37, Num 7, pp 692-700, issn 1061-4036, 9 p.Article

A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codonKONG, Xiao-Fei; VOGT, Guillaume; GONNORD, Pauline et al.Human molecular genetics (Print). 2010, Vol 19, Num 3, pp 434-444, issn 0964-6906, 11 p.Article

TLR3 deficiency in patients with herpes simplex encephalitisZHANG, Shen-Ying; JOUANGUY, Emmanuelle; PICARD, Capucine et al.Science (Washington, D.C.). 2007, Vol 317, Num 5844, pp 1522-1527, issn 0036-8075, 6 p.Article

Inherited disorders of the IL-12-IFN-γ axis in patients with disseminated BCG infectionMANSOURI, Davood; ADIMI, Parisa; VOGT, Guillaume et al.European journal of pediatrics. 2005, Vol 164, Num 12, pp 753-757, issn 0340-6199, 5 p.Article

Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindredsSOLOGUREN, Ithaisa; BOISSON-DUPUIS, Stéphanie; SANTIAGO, Esther et al.Human molecular genetics (Print). 2011, Vol 20, Num 8, pp 1509-1523, issn 0964-6906, 15 p.Article

SUCCESSFUL HEMATOPOIETIC STEM CELL TRANSPLANTATION FROM AN UNRELATED DONOR IN A CHILD WITH INTERFERON GAMMA RECEPTOR DEFICIENCYMOILANEN, Petra; KORPPI, Matti; HOVI, Liisa et al.The Pediatric infectious disease journal. 2009, Vol 28, Num 7, pp 658-660, issn 0891-3668, 3 p.Article

Inborn errors of interferon (IFN)-mediated immunity in humans : insights into the respective roles of IFN-α/β, IFN-y, and IFN-λ in host defenseZHANG, Shen-Ying; BOISSON-DUPUIS, Stéphanie; CHAPGIER, Ariane et al.Immunological reviews. 2008, Vol 226, pp 29-40, issn 0105-2896, 12 p.Article

Disseminated nontuberculous mycobacterial infection in a child with interferon-γ receptor 1 deficiencyTSOLIA, Maria N; CHAPGIER, Ariane; TAPRANTZI, Polyxeni et al.European journal of pediatrics. 2006, Vol 165, Num 7, pp 458-461, issn 0340-6199, 4 p.Article

Autosomal-dominant primary immunodeficiencies : Myeloid biologyLAWRENCE, Tatiana; PUEL, Anne; REICHENBACH, Janine et al.Current opinion in hematology. 2005, Vol 12, Num 1, pp 22-30, issn 1065-6251, 9 p.Article

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