Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("VARGA, Lilian")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 31

  • Page / 2
Export

Selection :

  • and

The use of 'real-time' complement analysis to differentiate atypical haemolytic uraemic syndrome from other forms of thrombotic microangiopathiesPROHASZKA, Zoltán; VARGA, Lilian; FÜST, George et al.British journal of haematology. 2012, Vol 158, Num 3, pp 424-425, issn 0007-1048, 2 p.Article

Parameters of the classical complement pathway predict disease severity in hereditary angioedemaCSUKA, Dorottya; FÜST, George; FARKAS, Henriette et al.Clinical immunology (Orlando, Fla. Print). 2011, Vol 139, Num 1, pp 85-93, issn 1521-6616, 9 p.Article

Prophylactic therapy in children with hereditary angioedemaFARKAS, Henriette; CSUKA, Dorottya; ZOTTER, Zsuzsanna et al.Journal of allergy and clinical immunology. 2013, Vol 131, Num 2, pp 579-582, issn 0091-6749, 4 p.Article

Complement activation in the nasal mucosa following nasal ragweed-allergen challengeMEZEI, Györgyi; VARGA, Lilian; VERES, Amarilla et al.Pediatric allergy and immunology. 2001, Vol 12, Num 4, pp 201-207, issn 0905-6157Article

Clinical management of hereditary angio-oedema in childrenFARKAS, Henriette; HARMAT, George; FÜST, George et al.Pediatric allergy and immunology. 2002, Vol 13, Num 3, pp 153-161, issn 0905-6157Article

Long-term efficacy of danazol treatment in hereditary angioedemaFÜST, George; FARKAS, Henriette; CSUKA, Dorottya et al.European journal of clinical investigation. 2011, Vol 41, Num 3, pp 256-262, issn 0014-2972, 7 p.Article

Monitoring the level of complement components during autologous blood stem cell transplantation in patients with malignant lymphomasBANYAI, Aniko; VARGA, Lilian; BARTA, Aniko et al.Cancer immunology and immunotherapy. 2004, Vol 53, Num 9, pp 835-839, issn 0340-7004, 5 p.Article

Eradication of Helicobacter pylori and improvement of hereditary angioneurotic oedemaFARKAS, Henriette; FÜST, George; FEKETE, Béla et al.Lancet (British edition). 2001, Vol 358, Num 9294, pp 1695-1696, issn 0140-6736Article

Lack of increased prevalence of immunoregulatory disorders in hereditary angioedema due to C1-inhibitor deficiencyFARKAS, Henriette; CSUKA, Dorottya; GACS, Judit et al.Clinical immunology (Orlando, Fla. Print). 2011, Vol 141, Num 1, pp 58-66, issn 1521-6616, 9 p.Article

Elevated complement C3 is associated with early restenosis after eversion carotid endarterectomySZEPLAKI, Gabor; VARGA, Lilian; FÜST, George et al.Thrombosis and haemostasis. 2006, Vol 96, Num 4, pp 529-534, issn 0340-6245, 6 p.Article

Activation of the ficolin-lectin pathway during attacks of hereditary angioedemaCSUKA, Dorottya; MUNTHE-FOG, Lea; HEIN, Estrid et al.Journal of allergy and clinical immunology. 2014, Vol 134, Num 6, pp 1388-1393, issn 0091-6749, 6 p.Article

Functional Cl-Inhibitor diagnostics in hereditary angioedema : Assay evaluation and recommendationsWAGENAAR-BOS, Ineke G. A; DROUET, Christian; HICKEY, Alaco et al.Journal of immunological methods. 2008, Vol 338, Num 1-2, pp 14-20, issn 0022-1759, 7 p.Article

Adverse effects of danazol prophylaxis on the lipid profiles of patients with hereditary angioedemaSZEPLAKI, Gabor; VARGA, Lilian; VALENTIN, Szilvia et al.Journal of allergy and clinical immunology. 2005, Vol 115, Num 4, pp 864-869, issn 0091-6749, 6 p.Article

Acquired Angioedema Associated with Primary Antiphospholipid Syndrome in a Patient with Antithrombin III DeficiencySZEPLAKI, Gabor; VARGA, Lilian; SZEPVÖLGYI, Aniko et al.International archives of allergy and immunology. 2008, Vol 146, Num 2, pp 164-168, issn 1018-2438, 5 p.Article

Recombinant human Cl-inhibitor in the treatment of acute angioedema attacksCHOI, Goda; SOETERS, Maarten R; LEVI, Marcel et al.Transfusion (Philadelphia, PA). 2007, Vol 47, Num 6, pp 1028-1032, issn 0041-1132, 5 p.Article

Deep venous thrombosis associated with acquired angioedema type II in a patient heterozygous for the mutation of factor V Leiden : Effective treatment and follow-up for four yearsSZEPLAKI, Gabor; VARGA, Lilian; OSVITH, Lilla et al.Thrombosis and haemostasis. 2006, Vol 95, Num 5, pp 898-899, issn 0340-6245, 2 p.Article

Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Lanagement of Hereditary AngioedemaBOWEN, Tom; CICARDI, Marco; ZURAW, Bruce et al.Journal of allergy and clinical immunology. 2004, Vol 114, Num 3, pp 629-637, issn 0091-6749, 9 p.Article

Functional analysis of the mannose-binding lectin complement pathway in normal pregnancy and preeclampsiaCSUKA, Dorottya; MOLVAREC, Attila; DERZSY, Zoltán et al.Journal of reproductive immunology. 2010, Vol 87, Num 1-2, pp 90-96, issn 0165-0378, 7 p.Article

High normal serum levels of C3 and C1 inhibitor, two acute-phase proteins belonging to the complement system, occur more frequently in patients with Crohn's disease than ulcerative colitisBENE, Laszlo; FÜST, George; VARGA, Lilian et al.Digestive diseases and sciences. 2003, Vol 48, Num 6, pp 1186-1192, issn 0163-2116, 7 p.Article

Angiooedema due to acquired deficiency of C1-esterase inhibitor associated with leucocytoclastic vasculitisFARKAS, Henriette; SZONGOTH, Mariann; BELY, Miklos et al.Acta dermato-venereologica. 2001, Vol 81, Num 4, pp 298-300, issn 0001-5555Article

Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?CSUKA, Dorottya; KELEMEN, Zsuzsanna; FARKAS, Henriette et al.European journal of gastroenterology & hepatology. 2011, Vol 23, Num 3, pp 238-244, issn 0954-691X, 7 p.Article

Strong complement activation after acute ischemic stroke is associated with unfavorable outcomesSZEPLAKI, Gabor; SZEGEDI, Róbert; FÜST, George et al.Atherosclerosis. 2009, Vol 204, Num 1, pp 315-320, issn 0021-9150, 6 p.Article

Hereditary angiodema : a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary AngioedemaBOWEN, Tom; CICARDI, Marco; WAGNER, Eric et al.Annals of allergy, asthma, & immunology. 2008, Vol 100, Num 1, issn 1081-1206, S30-S40, SUP2Article

Hereditary angioedema : A decade of human C1-inhibitor concentrate therapyFARKAS, Henriette; JAKAB, Laszlo; TEMESSZENTANDRASI, György et al.Journal of allergy and clinical immunology. 2007, Vol 120, Num 4, pp 941-947, issn 0091-6749, 7 p.Article

Ultrasonography in the diagnosis and monitoring of ascites in acute abdominal attacks of hereditary angioneurotic oedemaFARKAS, Henriette; HARMAT, George; KAPOSI, Pal N et al.European journal of gastroenterology & hepatology. 2001, Vol 13, Num 10, pp 1225-1230, issn 0954-691XArticle

  • Page / 2