Peter Arkwright
Peter Arkwright
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Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type IAutoantibodies in patients with …
A Puel, R Döffinger, A Natividad, M Chrabieh, G Barcenas-Morales, ...
The Journal of experimental medicine 207 (2), 291-297, 2010
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency
C Picard, H Von Bernuth, P Ghandil, M Chrabieh, O Levy, PD Arkwright, ...
Medicine 89 (6), 403, 2010
V(D)J recombination defects in lymphocytes due toRAG mutations: severe immunodeficiency with a spectrum of clinical presentations
A Villa, C Sobacchi, LD Notarangelo, F Bozzi, M Abinun, TG Abrahamsen, ...
Blood, The Journal of the American Society of Hematology 97 (1), 81-88, 2001
Effects of alcohol use and other aspects of lifestyle on blood pressure levels and prevalence of hypertension in a working population
PD Arkwright, LJ Beilin, I Rouse, BK Armstrong, R Vandongen
Circulation 60 (1), 60-66, 1982
B cell–intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans
DT Avery, EK Deenick, CS Ma, S Suryani, N Simpson, GY Chew, ...
Journal of Experimental Medicine 207 (1), 155-171, 2010
Autoimmune lymphoproliferative syndrome with somatic Fas mutations
E Holzelova, C Vonarbourg, MC Stolzenberg, PD Arkwright, F Selz, ...
New England Journal of Medicine 351 (14), 1409-1418, 2004
TGF-β1 genotype and accelerated decline in lung function of patients with cystic fibrosis
PD Arkwright, S Laurie, M Super, V Pravica, MJ Schwarz, AK Webb, ...
Thorax 55 (6), 459-462, 2000
Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations
S Okada, JG Markle, EK Deenick, F Mele, D Averbuch, M Lagos, ...
Science 349 (6248), 606-613, 2015
Functional STAT3 deficiency compromises the generation of human T follicular helper cells
CS Ma, DT Avery, A Chan, M Batten, J Bustamante, S Boisson-Dupuis, ...
Blood, The Journal of the American Society of Hematology 119 (17), 3997-4008, 2012
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 117 (1), 53-62, 2011
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome
C Woellner, EM Gertz, AA Schäffer, M Lagos, M Perro, EO Glocker, ...
Journal of Allergy and Clinical Immunology 125 (2), 424-432. e8, 2010
Intradermal administration of a killed Mycobacterium vaccae suspension (SRL 172) is associated with improvement in atopic dermatitis in children with moderate-to-severe disease
PD Arkwright, TJ David
Journal of allergy and clinical immunology 107 (3), 531-534, 2001
Autoimmunity in human primary immunodeficiency diseases
PD Arkwright, M Abinun, AJ Cant
Blood, The Journal of the American Society of Hematology 99 (8), 2694-2702, 2002
Clinical outcome in IL-10–and IL-10 receptor–deficient patients with or without hematopoietic stem cell transplantation
KR Engelhardt, N Shah, I Faizura-Yeop, DFK Uygun, N Frede, AM Muise, ...
Journal of Allergy and Clinical Immunology 131 (3), 825-830. e9, 2013
Human complete Stat-1 deficiency is associated with defective type I and II IFN responses in vitro but immunity to some low virulence viruses in vivo
A Chapgier, RF Wynn, E Jouanguy, O Filipe-Santos, S Zhang, J Feinberg, ...
The Journal of Immunology 176 (8), 5078-5083, 2006
Factors predicting anaphylaxis to peanuts and tree nuts in patients referred to a specialist center
CW Summers, RS Pumphrey, CN Woods, G McDowell, PW Pemberton, ...
Journal of Allergy and Clinical Immunology 121 (3), 632-638. e2, 2008
Clinical features that identify children with primary immunodeficiency diseases
A Subbarayan, G Colarusso, SM Hughes, AR Gennery, M Slatter, AJ Cant, ...
Pediatrics 127 (5), 810-816, 2011
Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease
A Chapgier, S Boisson-Dupuis, E Jouanguy, G Vogt, J Feinberg, ...
PLoS genetics 2 (8), e131, 2006
Lymphoproliferative syndrome with autoimmunity: a possible genetic basis for dominant expression of the clinical manifestations
F Rieux-Laucat, S Blachère, S Danielan, JP De Villartay, M Oleastro, ...
Blood, The Journal of the American Society of Hematology 94 (8), 2575-2582, 1999
Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type I
A Meloni, M Furcas, F Cetani, C Marcocci, A Falorni, R Perniola, M Pura, ...
The Journal of Clinical Endocrinology & Metabolism 93 (11), 4389-4397, 2008
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