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 *

360 related articles for article (PubMed ID: 28069032)

  • 21. 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]  

  • 22. 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]  

  • 23. Treatment response after repeated administration of C1 esterase inhibitor for successive acute hereditary angioedema attacks.
    Craig TJ; Bewtra AK; Hurewitz D; Levy R; Janss G; Jacobson KW; Packer F; Bernstein JA; Rojavin MA; Machnig T; Keinecke HO; Wasserman RL
    Allergy Asthma Proc; 2012; 33(4):354-61. PubMed ID: 22856636
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Type I hereditary angioedema in Taiwan -- clinical, biological features and genetic study.
    Lei WT; Shyur SD; Huang LH; Kao YH; Lo CY
    Asian Pac J Allergy Immunol; 2011 Dec; 29(4):327-31. PubMed ID: 22299312
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: a multicenter, prospective study.
    Savarese L; Bova M; De Falco R; Guarino MD; De Luca Picione R; Petraroli A; Senter R; Traverso C; Zabotto M; Zanichelli A; Zito E; Alessio M; Cancian M; Cicardi M; Franzese A; Perricone R; Marone G; Valerio P; Freda MF
    Orphanet J Rare Dis; 2018 Jul; 13(1):115. PubMed ID: 30005674
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Serum fetuin-A, tumor necrosis factor alpha and C-reactive protein concentrations in patients with hereditary angioedema with C1-inhibitor deficiency.
    Márkus B; Veszeli N; Temesszentandrási G; Farkas H; Kalabay L
    Orphanet J Rare Dis; 2019 Mar; 14(1):67. PubMed ID: 30885236
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Activation of the ficolin-lectin pathway during attacks of hereditary angioedema.
    Csuka D; Munthe-Fog L; Hein E; Zotter Z; Prohászka Z; Farkas H; Varga L; Garred P
    J Allergy Clin Immunol; 2014 Dec; 134(6):1388-1393.e1. PubMed ID: 25042985
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Management of dental-oral procedures in patients with hereditary angioedema due to C1 inhibitor deficiency.
    Jurado-Palomo J; Muñoz-Caro JM; López-Serrano MC; Prior N; Cabañas R; Pedrosa M; Burgueño M; Caballero T
    J Investig Allergol Clin Immunol; 2013; 23(1):1-6. PubMed ID: 23653967
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hereditary Angioedema Due to C1-Inhibitor Deficiency in Romania: First National Study, Diagnostic and Treatment Challenges.
    Gabos G; Nadasan V; Mihaly E; Dobru D
    Iran J Immunol; 2020 Sep; 17(3):226-235. PubMed ID: 32996899
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy.
    Farkas H; Jakab L; Temesszentandrási G; Visy B; Harmat G; Füst G; Széplaki G; Fekete B; Karádi I; Varga L
    J Allergy Clin Immunol; 2007 Oct; 120(4):941-7. PubMed ID: 17761272
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Treatment with C1-esterase inhibitor concentrate in type I or II hereditary angioedema: a systematic literature review.
    Bork K; Steffensen I; Machnig T
    Allergy Asthma Proc; 2013; 34(4):312-327. PubMed ID: 23710659
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII).
    Bork K; Wulff K; Witzke G; Hardt J
    Allergy; 2017 Feb; 72(2):320-324. PubMed ID: 27905115
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Elevated D-dimers in attacks of hereditary angioedema are not associated with increased thrombotic risk.
    Reshef A; Zanichelli A; Longhurst H; Relan A; Hack CE
    Allergy; 2015 May; 70(5):506-13. PubMed ID: 25640891
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Flow-mediated vasodilation assay indicates no endothelial dysfunction in hereditary angioedema patients with C1-inhibitor deficiency.
    Nebenführer Z; Szabó E; Kajdácsi E; Kőhalmi KV; Karádi I; Zsáry A; Farkas H; Cervenak L
    Ann Allergy Asthma Immunol; 2019 Jan; 122(1):86-92. PubMed ID: 30312677
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Efficacy and safety of recombinant human C1-inhibitor for the treatment of attacks of hereditary angioedema: European open-label extension study.
    Moldovan D; Reshef A; Fabiani J; Kivity S; Toubi E; Shlesinger M; Triggiani M; Montinaro V; Cillari E; Realdi G; Cancian M; Visscher S; Zanichelli A; Relan A; Cicardi M
    Clin Exp Allergy; 2012 Jun; 42(6):929-35. PubMed ID: 22909164
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.