Search Results - "Psarros, Fotis"
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Mitigating Disparity in Health-care Resources Between Countries for Management of Hereditary Angioedema
Published in Clinical reviews in allergy & immunology (01-08-2021)“…Hereditary angioedema (HAE) is a rare genetic disorder characterized by recurrent episodes of skin and mucosal edema. The main treatment goal is to enable a…”
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Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency
Published in Gene (15-08-2018)“…SERPING1 genotyping of subjects suspicious for hereditary angioedema due to C1-INH deficiency (C1-INH-HAE) is important for clinical practice as well as for…”
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The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency
Published in Clinical reviews in allergy & immunology (01-08-2021)“…Hereditary angioedema (HAE) is a rare condition, mostly due to genetic deficiency of complement C1 inhibitor (C1-INH). The rarity of HAE impedes extensive data…”
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Hereditary angioedema: Molecular and clinical differences among European populations
Published in Journal of allergy and clinical immunology (01-02-2015)“…Extending the bioinformatic analysis to all the 95 amino acid substitutions presented in HAEdb (C1 inhibiTor gene muTATion dATAbAse, available at…”
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A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency
Published in Allergology International (01-07-2020)“…In about 5% of patients with hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) no mutation in the SERPING1 gene is detected. C1-INH-HAE cases…”
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Hereditary angioedema in Greece: the first results of the greek hereditary angioedema registry
Published in International archives of allergy and immunology (01-01-2014)“…No published data presently exist concerning hereditary angioedema (HAE) in Greece. The aim of this study was to present the results from patients recorded by…”
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Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)
Published in Frontiers in allergy (07-07-2022)“…Existing evidence indicates that modifier genes could change the phenotypic outcome of the causal SERPING1 variant and thus explain the expression variability…”
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Efficacy of a Quail Eggs-Based Dietary Supplement for Allergic Rhinitis: Results of a Single-Arm Trial
Published in Journal of dietary supplements (02-01-2021)“…Previous data suggested the potential treatment effect of a proprietary quail eggs-based blend on allergic rhinitis (AR) symptoms, induced by allergen…”
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Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE‐PLG patients
Published in Allergy (Copenhagen) (01-08-2020)Get full text
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Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks
Published in The New England journal of medicine (04-07-2024)“…In this trial involving 264 hereditary angioedema attacks, oral sebetralstat provided faster times to the beginning of symptom relief, reduction in attack…”
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The Rate of Atopy in Patients with Cold-Induced Urticaria
Published in Journal of allergy and clinical immunology (01-02-2017)“…Demographic, clinical and laboratory test results, including age, gender, age at symptoms onset, personal and family history of atopy, total and specific IgE…”
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Levels of IgE sensitization drive symptom thresholds in allergic rhinitis
Published in Annals of allergy, asthma, & immunology (01-08-2024)“…Allergic rhinitis (AR) is a common respiratory disease encompassing a variety of phenotypes. Patients can be sensitized to 1 or more allergens. There are…”
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Heterogeneity of pollen food allergy syndrome in seven Southern European countries: The @IT.2020 multicenter study
Published in Allergy (Copenhagen) (01-10-2021)“…Background Pollen food allergy syndrome (PFAS) is a frequently underdiagnosed disease due to diverse triggers, clinical presentations, and test results. This…”
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“Whole” vs. “fragmented” approach to EAACI pollen season definitions: A multicenter study in six Southern European cities
Published in Allergy (Copenhagen) (01-07-2020)“…Background The adequate definition of pollen seasons is essential to facilitate a correct diagnosis, treatment choice, and outcome assessment in patients with…”
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International Consensus on the Use of Genetics in the Management of Hereditary Angioedema
Published in The journal of allergy and clinical immunology in practice (Cambridge, MA) (01-03-2020)“…Hereditary angioedema (HAE) is becoming much more genetically complex than was initially considered. Thus, the role of HAE genetics is expanding beyond…”
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Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor
Published in Journal of clinical medicine (23-10-2020)“…The genetic alteration underlying the great majority of primary angioedema with normal C1 inhibitor (nl-C1-INH-HAE) cases remains unknown. To search for…”
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Levels of Immunoglobulin E Sensitization Drive Symptom Thresholds in Allergic Rhinitis
Published in Annals of allergy, asthma, & immunology (26-04-2024)“…Allergic rhinitis (AR) is a common respiratory disease encompassing a variety of phenotypes. Patients can be sensitized to one or more allergens. There are…”
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Mobile technology offers novel insights into the control and treatment of allergic rhinitis: The MASK study
Published in Journal of allergy and clinical immunology (01-07-2019)Get full text
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Validity, reliability, and responsiveness of daily monitoring visual analog scales in MASK‐air
Published in Clinical and translational allergy (01-09-2021)“…Abstract Background MASK‐air® is an app that supports allergic rhinitis patients in disease control. Users register daily allergy symptoms and their impact on…”
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322 Preoperative Cardiopulmonary Exercise Testing (CPET) in Severe Asthma Patients
Published in The World Allergy Organization journal (17-02-2012)Get full text
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