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Beata Derfalvi
Beata Derfalvi
Verified email at iwk.nshealth.ca
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Cited by
Cited by
Year
Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU
B Neven, I Callebaut, AM Prieur, J Feldmann, C Bodemer, L Lepore, ...
Blood 103 (7), 2809-2815, 2004
3692004
Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update
European Society for Immunodeficiencies (ESID) members de Vries E esid ...
Clinical & Experimental Immunology 167 (1), 108-119, 2012
1872012
Improved flow cytometric assessment reveals distinct microvesicle (cell-derived microparticle) signatures in joint diseases
B György, TG Szabó, L Turiák, M Wright, P Herczeg, Z Lédeczi, Á Kittel, ...
PloS one 7 (11), e49726, 2012
1862012
Similarities and differences between pediatric and adult patients with systemic lupus erythematosus
T Tarr, B Dérfalvi, N Győri, A Szántó, Z Siminszky, A Malik, AJ Szabó, ...
Lupus 24 (8), 796-803, 2015
1422015
X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world
ZA El-Sayed, I Abramova, JC Aldave, W Al-Herz, L Bezrodnik, R Boukari, ...
World Allergy Organization Journal 12 (3), 100018, 2019
1112019
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups
H Jiao, B Tóth, M Erdős, I Fransson, É Rákóczi, I Balogh, Z Magyarics, ...
Molecular immunology 46 (1), 202-206, 2008
1012008
Therapeutic options for CTLA-4 insufficiency
D Egg, IC Rump, N Mitsuiki, J Rojas-Restrepo, ME Maccari, C Schwab, ...
Journal of Allergy and Clinical Immunology 149 (2), 736-746, 2022
772022
Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study
B Tóth, A Volokha, A Mihas, M Pac, E Bernatowska, I Kondratenko, ...
Molecular immunology 46 (10), 2140-2146, 2009
702009
National registry of patients with juvenile idiopathic inflammatory myopathies in Hungary—clinical characteristics and disease course of 44 patients with juvenile dermatomyositis
T Constantin, T Constantin, A Ponyi, T Constantin, A Ponyi, I Orbán, ...
Autoimmunity 39 (3), 223-232, 2006
612006
Efficacy, safety, tolerability and pharmacokinetics of a novel human immune globulin subcutaneous, 20%: a Phase 2/3 study in Europe in patients with primary immunodeficiencies
M Borte, G Kriván, B Dérfalvi, L Marodi, T Harrer, S Jolles, C Bourgeois, ...
Clinical & Experimental Immunology 187 (1), 146-159, 2017
492017
Rheumatic symptoms in childhood leukaemia and lymphoma-a ten-year retrospective study
L Zombori, G Kovacs, M Csoka, B Derfalvi
Pediatric Rheumatology 11, 1-5, 2013
492013
Genetic variants of the interleukin-18 promoter region (-607) influence the course of necrotising enterocolitis in very low birth weight neonates
E Héninger, A Treszl, I Kocsis, B Dérfalvi, T Tulassay, B Vá sá rhelyi
European journal of pediatrics 161, 410-411, 2002
492002
Interleukin-6-induced production of type II acute phase proteins and expression of junB gene are downregulated by human recombinant growth hormone in vitro
B Derfalvi, P Igaz, KA Fulop, C Szalai, A Falus
Cell Biology International 24 (2), 109-114, 2000
372000
COVID-19 vaccine testing & administration guidance for allergists/immunologists from the Canadian Society of Allergy and Clinical Immunology (CSACI)
TK Vander Leek, ES Chan, L Connors, B Derfalvi, AK Ellis, JEM Upton, ...
Allergy, Asthma & Clinical Immunology 17, 1-6, 2021
342021
B cell development in chromosome 22q11. 2 deletion syndrome
B Derfalvi, K Maurer, DMMD McGinn, E Zackai, W Meng, ETL Prak, ...
Clinical Immunology 163, 1-9, 2016
302016
Rituximab-induced hypogammaglobulinemia and infection risk in pediatric patients
R Labrosse, S Barmettler, B Derfalvi, A Blincoe, G Cros, ...
Journal of Allergy and Clinical Immunology 148 (2), 523-532. e8, 2021
292021
Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity
M Haimel, J Pazmandi, RJ Heredia, J Dmytrus, SK Bal, S Zoghi, ...
Journal of Allergy and Clinical Immunology 149 (1), 369-378, 2022
262022
Molecular genetic analysis of Hungarian patients with the hyper-immunoglobulin M syndrome
M Erdős, G Lakos, B Dérfalvi, LD Notarangelo, A Durandy, L Maródi
Molecular immunology 45 (1), 278-282, 2008
152008
Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins
N Alrumayyan, D Slauenwhite, SM McAlpine, S Roberts, TB Issekutz, ...
Allergy, Asthma & Clinical Immunology 18 (1), 17, 2022
142022
High dose intravenous IgG therapy modulates multiple NK cell and T cell functions in patients with immune dysregulation
SM McAlpine, SE Roberts, JJ Heath, F Käsermann, AC Issekutz, ...
Frontiers in Immunology 12, 660506, 2021
142021
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