» Authors » Wojciech Dyga

Wojciech Dyga

Explore the profile of Wojciech Dyga including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 30
Citations 67
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Czarnobilska M, Bulanda M, Czarnobilska E, Dyga W, Mazur M
Diagnostics (Basel) . 2024 Sep; 14(18). PMID: 39335714
The diagnosis of drug-induced anaphylaxis (DIA) is a serious health problem. The Basophil activation test (BAT) is considered a specific in vitro provocation, and compared to in vivo provocation, it...
2.
Korosec P, Sturm G, Lyons J, Marolt T, Svetina M, Kosnik M, et al.
Allergy . 2024 Mar; 79(9):2458-2469. PMID: 38477502
Background: In patients who require venom immunotherapy (VIT), there is a need to identify underlying mast cell (MC) disorders since these may affect the risk and severity of future sting...
3.
Mazur M, Dyga W, Czarnobilska E
J Clin Med . 2023 Sep; 12(18). PMID: 37762923
Atopic dermatitis (AD) prevalence in Poland is more frequent in individuals who live in a city. There are more studies demonstrating that long-term exposure to air pollutants is an independent...
4.
Dyga W, Obtulowicz A, Mikolajczyk T, Bogdali A, Dubiela P, Obtulowicz K
Int J Mol Sci . 2022 Sep; 23(18). PMID: 36142237
Background: Hereditary angioedema (HAE) is a rare, genetic disease caused by the decreased level or function of the C1 inhibitor. The primary mediator of symptoms in HAE is bradykinin acting...
5.
Obtulowicz P, Stobiecki M, Dyga W, Juchacz A, Popiela T, Obtulowicz K
Postepy Dermatol Alergol . 2022 Sep; 39(4):749-756. PMID: 36090726
Introduction: Hereditary angioedema (HAE) is a rare inherited autosomal dominant disease caused by deficiency or dysfunction of C1 inhibitor (C1INH). Clinical symptoms include recurrent subcutaneous and submucosal angioedema of the...
6.
Mazur M, Czarnobilska M, Dyga W, Czarnobilska E
J Clin Med . 2022 Apr; 11(8). PMID: 35456279
The prevalence of asthma and allergies among children has become an increasing problem in the last few decades. Data on the population of children and adolescents, especially living in polluted...
7.
Obtulowicz A, Dubiela P, Dyga W, Migacz-Gruszka K, Mikolajczyk T, Wojas-Pelc A, et al.
Medicina (Kaunas) . 2021 Oct; 57(10). PMID: 34684170
Chronic spontaneous urticaria (CSU) is a distressing skin condition, which manifests as red, swollen, itchy, and sometimes painful hives or wheals appearing on skin. Recently, CSU has been associated with...
8.
Obtulowicz K, Ksiazek T, Bogdali A, Dyga W, Czarnobilska E, Juchacz A
Cent Eur J Immunol . 2021 Jan; 45(3):301-309. PMID: 33437182
Hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) type I and II is a rare and life-threatening disease caused by SERPING1 gene mutations. Previous genetic studies indicated a wide spectrum of...
9.
Obtulowicz K, Goralska J, Bogdali A, Dyga W, Obtulowicz A, Myszkowska D, et al.
Pol Arch Intern Med . 2020 Jan; 130(2):79-88. PMID: 31933486
Introduction: Hereditary angioedema (HAE) is a rare autosomal dominant disease caused by genetic dysfunction of C1 inhibitor (C1-INH) due to mutations in the SERPING1 gene. The disorder is mediated mainly...
10.
Obtulowicz K, Dyga W, Natorska J, Zabczyk M, Undas A
Pol Arch Intern Med . 2019 Dec; 129(12):936-938. PMID: 31814604
No abstract available.