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Journal Abstract Search

175 related items for PubMed ID: 31616213

  • 1. A hereditary angioedema screening in two villages, based on an index case, and identification of a novel mutation, "1033G>T", at the SERPING1 gene.
    Ozkars MY, Keskın O, Bayram N, Onay H, Keskın M, Bayram H, Sahın Y, Küçükosmanoğlu E, Kırık S.
    Postepy Dermatol Alergol; 2019 Aug; 36(4):403-411. PubMed ID: 31616213
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  • 3. A hereditary angioedema screening on an index case: Turkey.
    Ozkars MY, Keskin O, Bayram N, Keskin M, Bayram H, Sahin Y, Kucukosmanoglu E, Attila N, Kirik SK.
    Asian Pac J Allergy Immunol; 2019 Sep; 37(3):154-161. PubMed ID: 30118244
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  • 5. Case Report: Early presentation of hereditary angioedema symptoms in a 2-year-old boy.
    Staikuniene-Kozonis J, Staikunaite J, Gasiuniene E, Sematonyte J.
    Front Pediatr; 2024 Sep; 12():1408110. PubMed ID: 38978843
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  • 8. Recessive SERPING1 Variant Leads to Kinin-Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary Angioedema.
    Maia LSM, Burger B, Ghannam A, Nunes FL, Ferriani MPL, Dias MM, Arruda LK, Drouet C, Cichon S.
    J Clin Med; 2023 Nov 24; 12(23):. PubMed ID: 38068351
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  • 10. Genetic variants of SERPING1 gene in Polish patients with hereditary angioedema due to C1 inhibitor deficiency.
    Obtulowicz K, KsiĄŻek T, Bogdali A, Dyga W, Czarnobilska E, Juchacz A.
    Cent Eur J Immunol; 2020 Nov 24; 45(3):301-309. PubMed ID: 33437182
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  • 14. Complex analysis of the national Hereditary angioedema cohort in Slovakia - Identification of 12 novel variants in SERPING1 gene.
    Markocsy A, Hrubiskova K, Hrubisko M, Freiberger T, Grombirikova H, Dolesova L, Slivka Vavrova L, Lohajova Behulova R, Ondrusova M, Banovcin P, Vorcakova K, Jesenak M.
    World Allergy Organ J; 2024 Mar 24; 17(3):100885. PubMed ID: 38486718
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  • 17. Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.
    Loules G, Zamanakou M, Parsopoulou F, Vatsiou S, Psarros F, Csuka D, Porebski G, Obtulowicz K, Valerieva A, Staevska M, López-Lera A, López-Trascasa M, Moldovan D, Magerl M, Maurer M, Speletas M, Farkas H, Germenis AE.
    Gene; 2018 Aug 15; 667():76-82. PubMed ID: 29753808
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  • 18. Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE).
    Parsopoulou F, Loules G, Zamanakou M, Csuka D, Szilagyi A, Kompoti M, Porebski G, Psarros F, Magerl M, Valerieva A, Staevska M, Obtulowicz K, Maurer M, Speletas M, Farkas H, Germenis AE.
    Front Allergy; 2022 Aug 15; 3():868185. PubMed ID: 35873600
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  • 19. C1 inhibitor gene expression in patients with hereditary angioedema: quantitative evaluation by means of real-time RT-PCR.
    Pappalardo E, Zingale LC, Cicardi M.
    J Allergy Clin Immunol; 2004 Sep 15; 114(3):638-44. PubMed ID: 15356570
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  • 20. Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort.
    Grombirikova H, Bily V, Soucek P, Kramarek M, Hakl R, Ballonova L, Ravcukova B, Ricna D, Kozena K, Kratochvilova L, Sobotkova M, Zachova R, Kuklinek P, Kralickova P, Krcmova I, Hanzlikova J, Vachova M, Krystufkova O, Dankova E, Jesenak M, Novackova M, Svoboda M, Litzman J, Freiberger T.
    J Clin Immunol; 2023 Nov 15; 43(8):1974-1991. PubMed ID: 37620742
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