These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 26895475)

  • 1. Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain.
    Jaradat SA; Caccia S; Rawashdeh R; Melhem M; Al-Hawamdeh A; Carzaniga T; Haddad H
    Mol Immunol; 2016 Mar; 71():123-130. PubMed ID: 26895475
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. 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]  

  • 5. Hereditary angioedema nationwide study in Slovenia reveals four novel mutations in SERPING1 gene.
    Rijavec M; Korošec P; Šilar M; Zidarn M; Miljković J; Košnik M
    PLoS One; 2013; 8(2):e56712. PubMed ID: 23437219
    [TBL] [Abstract][Full Text] [Related]  

  • 6. F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.
    Speletas M; Szilágyi Á; Csuka D; Koutsostathis N; Psarros F; Moldovan D; Magerl M; Kompoti M; Varga L; Maurer M; Farkas H; Germenis AE
    Allergy; 2015 Dec; 70(12):1661-4. PubMed ID: 26248961
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Paternal mosaicism and hereditary angioedema in a Taiwanese family.
    Yu TC; Shyur SD; Huang LH; Wen DC; Li JS
    Ann Allergy Asthma Immunol; 2007 Oct; 99(4):375-9. PubMed ID: 17941288
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 114(3):638-44. PubMed ID: 15356570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Normal C1 inhibitor mRNA expression level in type I hereditary angioedema patients: newly found C1 inhibitor gene mutations.
    Kang HR; Yim EY; Oh SY; Chang YS; Kim YK; Cho SH; Min KU; Kim YY
    Allergy; 2006 Feb; 61(2):260-4. PubMed ID: 16409206
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of SERPING1 expression on hereditary angioedema patients: quantitative analysis of full-length and exon 3 splicing variants.
    de la Cruz RM; López-Lera A; López-Trascasa M
    Immunol Lett; 2012 Jan; 141(2):158-64. PubMed ID: 22001489
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema.
    Cagini N; Veronez CL; Constantino-Silva RN; Buzolin M; Martin RP; Grumach AS; Velloso LA; Mansour E; Pesquero JB
    Biol Chem; 2016 Apr; 397(4):337-44. PubMed ID: 26812872
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel and recurrent mutations in the C1NH gene of Arab patients affected with hereditary angioedema.
    Faiyaz-Ul-Haque M; Al-Gazlan S; Abalkhail HA; Al-Abdulatif A; Toulimat M; Peltekova I; Khaliq AM; Al-Dayel F; Zaidi SH
    Int Arch Allergy Immunol; 2010; 151(2):149-54. PubMed ID: 19752569
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor.
    Dewald G
    Biochem Biophys Res Commun; 2018 Mar; 498(1):193-198. PubMed ID: 29548426
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a novel and recurrent mutation in the SERPING1 gene in patients with hereditary angioedema.
    Firinu D; Colomba P; Manconi PE; Barca MP; Fenu L; Piseddu G; Zizzo C; Del Giacco SR; Duro G
    Clin Immunol; 2013 May; 147(2):129-32. PubMed ID: 23583915
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family.
    Ferraro MF; Moreno AS; Castelli EC; Donadi EA; Palma MS; Arcuri HA; Lange AP; Bork K; Sarti W; Arruda LK
    Allergy; 2011 Oct; 66(10):1384-90. PubMed ID: 21623829
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema.
    Szabó E; Csuka D; Andrási N; Varga L; Farkas H; Szilágyi Á
    Front Allergy; 2022; 3():836465. PubMed ID: 35386643
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.
    Moreno AS; Valle SO; Levy S; França AT; Serpa FS; Arcuri HA; Palma MS; Campos WN; Dias MM; Ponard D; Monnier N; Lunardi J; Bork K; Silva WA; Arruda LK
    Int Arch Allergy Immunol; 2015; 166(2):114-20. PubMed ID: 25790805
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation.
    Hujová P; Souček P; Grodecká L; Grombiříková H; Ravčuková B; Kuklínek P; Hakl R; Litzman J; Freiberger T
    J Clin Immunol; 2020 Apr; 40(3):435-446. PubMed ID: 31982983
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.