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 *

244 related articles for article (PubMed ID: 23437219)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Mutation screening of the C1 inhibitor gene among Hungarian patients with hereditary angioedema.
    Kalmár L; Bors A; Farkas H; Vas S; Fandl B; Varga L; Füst G; Tordai A
    Hum Mutat; 2003 Dec; 22(6):498. PubMed ID: 14635117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations.
    Blanch A; Roche O; López-Granados E; Fontán G; López-Trascasa M
    Hum Mutat; 2002 Nov; 20(5):405-6. PubMed ID: 12402344
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema.
    Freiberger T; Kolárová L; Mejstrík P; Vyskocilová M; Kuklínek P; Litzman J
    Hum Mutat; 2002 Apr; 19(4):461. PubMed ID: 11933207
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations analysis of C1 inhibitor coding sequence gene among Portuguese patients with hereditary angioedema.
    Martinho A; Mendes J; Simões O; Nunes R; Gomes J; Dias Castro E; Leiria-Pinto P; Ferreira MB; Pereira C; Castel-Branco MG; Pais L
    Mol Immunol; 2013 Apr; 53(4):431-4. PubMed ID: 23123409
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations).
    Nabilou S; Pak F; Alizadeh Z; Fazlollahi MR; Houshmand M; Ayazi M; Mohammadzadeh I; Bemanian MH; Fayezi A; Nabavi M; Saghafi S; Mohammadian S; Kokhaei P; Moin M; Pourpak Z
    Immunol Invest; 2022 Jan; 51(1):170-181. PubMed ID: 32896191
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary angioedema caused by a premature stop codon mutation in the SERPING1 gene.
    Xu YY; Gu JQ; Zhi YX
    Clin Transl Allergy; 2020 Nov; 10(1):53. PubMed ID: 33292549
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of C1 inhibitor mutations in patients with hereditary angioedema.
    Zuraw BL; Herschbach J
    J Allergy Clin Immunol; 2000 Mar; 105(3):541-6. PubMed ID: 10719305
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.