BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 33469833)

  • 1. In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency.
    Loli-Ausejo D; López-Lera A; Drouet C; Lluncor M; Phillips-Anglés E; Pedrosa M; Cabañas R; Caballero T
    Clin Rev Allergy Immunol; 2021 Aug; 61(1):1-14. PubMed ID: 33469833
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.
    Grivčeva-Panovska V; Košnik M; Korošec P; Andrejević S; Karadža-Lapić L; Rijavec M
    Ann Med; 2018 May; 50(3):269-276. PubMed ID: 29513108
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association.
    Andrejević S; Korošec P; Šilar M; Košnik M; Mijanović R; Bonači-Nikolić B; Rijavec M
    PLoS One; 2015; 10(11):e0142174. PubMed ID: 26535898
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.
    Vatsiou S; Zamanakou M; Loules G; Psarros F; Parsopoulou F; Csuka D; Valerieva A; Staevska M; Porebski G; Obtulowicz K; Magerl M; Maurer M; Speletas M; Farkas H; Germenis AE
    Allergol Int; 2020 Jul; 69(3):443-449. PubMed ID: 31959500
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.
    Ponard D; Gaboriaud C; Charignon D; Ghannam A; Wagenaar-Bos IGA; Roem D; López-Lera A; López-Trascasa M; Tosi M; Drouet C
    Hum Mutat; 2020 Jan; 41(1):38-57. PubMed ID: 31517426
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetics of Hereditary Angioedema Revisited.
    Germenis AE; Speletas M
    Clin Rev Allergy Immunol; 2016 Oct; 51(2):170-82. PubMed ID: 27116602
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology.
    Sinnathamby ES; Issa PP; Roberts L; Norwood H; Malone K; Vemulapalli H; Ahmadzadeh S; Cornett EM; Shekoohi S; Kaye AD
    Adv Ther; 2023 Mar; 40(3):814-827. PubMed ID: 36609679
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletions in SERPING1 Lead to Lower C1 Inhibitor Function: Lower C1 Inhibitor Function Can Predict Disease Severity.
    Mete Gökmen N; Gülbahar O; Onay H; Peker Koc Z; Özgül S; Köse T; Gelincik A; Büyüköztürk S; Sin AZ
    Int Arch Allergy Immunol; 2019; 178(1):50-59. PubMed ID: 30278448
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes.
    Bork K; Zibat A; Ferrari DM; Wollnik B; Schön MP; Wulff K; Lippert U
    J Dtsch Dermatol Ges; 2020 Mar; 18(3):215-223. PubMed ID: 32065705
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.
    Karadža-Lapić L; Korošec P; Šilar M; Košnik M; Cikojević D; Lozić B; Rijavec M
    Ann Med; 2016 Nov; 48(7):485-491. PubMed ID: 27187751
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Definition and classification of hereditary angioedema.
    Proper SP; Lavery WJ; Bernstein JA
    Allergy Asthma Proc; 2020 Nov; 41(Suppl 1):S03-S07. PubMed ID: 33109317
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency.
    Rupar N; Šelb J; Košnik M; Zidarn M; Andrejević S; Čulav L; Grivčeva-Panovska V; Korošec P; Rijavec M
    Gene; 2024 Aug; 919():148496. PubMed ID: 38679185
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.
    Bork K; Wulff K; Witzke G; Hardt J
    Allergy; 2015 Aug; 70(8):1004-12. PubMed ID: 25952149
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 667():76-82. PubMed ID: 29753808
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1.
    Johnsrud I; Kulseth MA; Rødningen OK; Landrø L; Helsing P; Waage Nielsen E; Heimdal K
    PLoS One; 2015; 10(7):e0131637. PubMed ID: 26154504
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 43(8):1974-1991. PubMed ID: 37620742
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene.
    Sharma J; Jindal AK; Banday AZ; Kaur A; Rawat A; Singh S; Longhurst H
    Clin Rev Allergy Immunol; 2021 Jun; 60(3):305-315. PubMed ID: 33442779
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Insights into the pathogenesis of hereditary angioedema using genetic sequencing and recombinant protein expression analyses.
    Ren Z; Zhao S; Li T; Wedner HJ; Atkinson JP
    J Allergy Clin Immunol; 2023 Apr; 151(4):1040-1049.e5. PubMed ID: 36587848
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational spectrum of the SERPING1 gene in Swiss patients with hereditary angioedema.
    Steiner UC; Keller M; Schmid P; Cichon S; Wuillemin WA
    Clin Exp Immunol; 2017 Jun; 188(3):430-436. PubMed ID: 28194776
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset.
    Gianni P; Loules G; Zamanakou M; Kompoti M; Csuka D; Psarros F; Magerl M; Moldovan D; Maurer M; Speletas MG; Farkas H; Germenis AE
    Int Arch Allergy Immunol; 2017; 174(3-4):200-204. PubMed ID: 29130992
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.