Search Results - "Zotter, Zsuzsanna"

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  1. 1

    The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency by Zotter, Zsuzsanna, Csuka, Dorottya, Szabó, Erika, Czaller, Ibolya, Nébenführer, Zsuzsanna, Temesszentandrási, György, Fust, George, Varga, Lilian, Farkas, Henriette

    Published in Orphanet journal of rare diseases (28-03-2014)
    “…Hereditary angioedema (HAE) resulting from C1-inhibitor deficiency is characterized by attacks of subcutaneous and submucosal edema. Many factors have been…”
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    Journal Article
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    Activation of the ficolin-lectin pathway during attacks of hereditary angioedema by Csuka, Dorottya, PhD, Munthe-Fog, Lea, PhD, Hein, Estrid, MSc, Zotter, Zsuzsanna, MD, Prohászka, Zoltán, MD, PhD, DSc, Farkas, Henriette, MD, PhD, DSc, Varga, Lilian, PhD, Garred, Peter, MD, PhD, DSc

    Published in Journal of allergy and clinical immunology (01-12-2014)
    “…Background The activation of plasma enzyme systems is insufficiently controlled in hereditary angioedema due to the deficiency of C1-inhibitor (C1-INH)…”
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    Prophylactic therapy in children with hereditary angioedema by Farkas, Henriette, MD, PhD, DSc, Csuka, Dorottya, MSc, Zotter, Zsuzsanna, MD, Varga, Lilian, PhD, Füst, George, MD, PhD, DSc

    Published in Journal of allergy and clinical immunology (01-02-2013)
    “…According to the guidelines, antifibrinolytics are the agents of choice for prophylaxis in pediatric patients.6 Their use is seldom contraindicated;…”
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    Lack of increased prevalence of immunoregulatory disorders in hereditary angioedema due to C1-inhibitor deficiency by Farkas, Henriette, Csuka, Dorottya, Gács, Judit, Czaller, Ibolya, Zotter, Zsuzsanna, Füst, George, Varga, Lilian, Gergely, Péter

    Published in Clinical immunology (Orlando, Fla.) (01-10-2011)
    “…Abstract Hereditary angioedema due to deficiency of C1-INH (HAE-C1-INH) is associated with enhanced consumption of the early complement components, which may…”
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    Thyroid hormones and complement parameters in hereditary angioedema with C1-inhibitor deficiency by Czaller, Ibolya, MD, Csuka, Dorottya, PhD, Zotter, Zsuzsanna, MD, Veszeli, Nóra, MSc, Takács, Edit, MD, Imreh, Éva, MD, Varga, Lilian, PhD, Farkas, Henriette, MD, PhD, DSc

    Published in Annals of allergy, asthma, & immunology (01-08-2016)
    “…Abstract Background Thyroid hormones control and up-regulate the synthesis of many plasma proteins. Objective To explore possible associations between thyroid…”
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    Short-term prophylaxis in a patient with acquired C1-INH deficiency by Farkas, Henriette, MD, PhD, DSc, Kőhalmi, Kinga Viktória, Zotter, Zsuzsanna, MD, Csuka, Dorottya, PhD, Molnár, Katalin, MD, Benedek, Szabolcs, MD, Varga, Lilian, PhD

    Published in Journal of allergy and clinical immunology (01-08-2014)
    “…AAE-C1-INH was diagnosed from the clinical symptoms, the complement screen (Table I), and the negative family history. Because the known trigger factors of…”
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    The role of ficolins and MASPs in hereditary angioedema due to C1-inhibitor deficiency by Csuka, Dorottya, Munthe-Fog, Lea, Skjoedt, Mikkel-Ole, Kocsis, Andrea, Zotter, Zsuzsanna, Gál, Péter, Varga, Lilian, Farkas, Henriette, Füst, George, Garred, Peter

    Published in Molecular immunology (01-07-2013)
    “…► The lectin pathway parameters were different between HAE patients and controls. ► Severe hereditary angioedema is associated with lower ficolin-2 and…”
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    Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency by Csuka, Dorottya, Veszeli, Nóra, Imreh, Éva, Zotter, Zsuzsanna, Skopál, Judit, Prohászka, Zoltán, Varga, Lilian, Farkas, Henriette

    Published in Orphanet journal of rare diseases (09-10-2015)
    “…The activation of plasma enzyme systems contributes to hereditary angioedema attacks. We aimed to study the activation markers of the fibrinolytic,…”
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    Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema by Zotter, Zsuzsanna, Veszeli, Nóra, Csuka, Dorottya, Varga, Lilian, Farkas, Henriette

    Published in Orphanet journal of rare diseases (05-12-2014)
    “…Danazol, a drug extensively used in the management of hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE), has various side effects. This study…”
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    Neutrophil activation during attacks in patients with hereditary angioedema due to C1-inhibitor deficiency by Veszeli, Nóra, Csuka, Dorottya, Zotter, Zsuzsanna, Imreh, Éva, Józsi, Mihály, Benedek, Szabolcs, Varga, Lilian, Farkas, Henriette

    Published in Orphanet journal of rare diseases (10-12-2015)
    “…Earlier studies have shown that the absolute number of neutrophil granulocytes (NGs) may increase during attack of hereditary angioedema due to C1-inhibitor…”
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    Risk of thromboembolism in patients with hereditary angioedema treated with plasma-derived C1-inhibitor by Farkas, Henriette, Kőhalmi, Kinga V, Veszeli, Nóra, Zotter, Zsuzsanna, Várnai, Katalin, Varga, Lilian

    Published in Allergy and asthma proceedings (01-03-2016)
    “…Plasma-derived C1-inhibitor (C1-INH) concentrates (pdC1-INH) have been used as safe and effective treatments for hereditary angioedema with C1-INH deficiency…”
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    Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency by Zotter, Zsuzsanna, Nagy, Zsolt, Patócs, Attila, Csuka, Dorottya, Veszeli, Nóra, Kőhalmi, Kinga Viktória, Farkas, Henriette

    Published in Orphanet journal of rare diseases (10-01-2017)
    “…Hereditary angioedema caused by C1-inhibitor deficiency (C1-INH-HAE) is a rare, autosomal dominant disorder. C1-INH-HAE is characterized by edema-formation,…”
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    The effect of long-term danazol treatment on haematological parameters in hereditary angioedema by Kőhalmi, Kinga Viktória, Veszeli, Nóra, Zotter, Zsuzsanna, Csuka, Dorottya, Benedek, Szabolcs, Imreh, Éva, Varga, Lilian, Farkas, Henriette

    Published in Orphanet journal of rare diseases (25-02-2016)
    “…The 17-alpha-alkylated derivatives of testosterone are often used for the prevention of oedematous episodes in hereditary angioedema with C1-inhibitor…”
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    Home treatment of attacks with conestat alfa in hereditary angioedema due to C1-inhibitor deficiency by Farkas, Henriette, Csuka, Dorottya, Veszeli, Nóra, Zotter, Zsuzsanna, Szabó, Erika, Varga, Lilian

    Published in Allergy and asthma proceedings (01-05-2014)
    “…Conestat alfa, a recombinant human C1 inhibitor (rhC1-INH) is a novel therapeutic option for the acute treatment of hereditary angioedema due to C1-INH…”
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