BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 30267321)

  • 41. Recombinant human C1 esterase inhibitor in the management of hereditary angioedema.
    Riedl M
    Clin Drug Investig; 2015 Jul; 35(7):407-17. PubMed ID: 26091744
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Factor VII activating protease (FSAP) is not essential in the pathophysiology of angioedema in patients with C1 inhibitor deficiency.
    Gramstad OR; Kandanur SPS; Etscheid M; Nielsen EW; Kanse SM
    Mol Immunol; 2022 Feb; 142():95-104. PubMed ID: 34973499
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Efficacy of lanadelumab in acquired angioedema with C1-inhibitor deficiency.
    Belbézier A; Boccon-Gibod I; Bouillet L
    J Allergy Clin Immunol Pract; 2021 Jun; 9(6):2490-2491. PubMed ID: 33556593
    [No Abstract]   [Full Text] [Related]  

  • 44. Pathogenic variant in
    Kron K; Joshi S
    BMJ Case Rep; 2023 Nov; 16(11):. PubMed ID: 37923334
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.
    Zeerleder S; Levi M
    Ann Med; 2016; 48(4):256-67. PubMed ID: 27018196
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Lanadelumab in Patients 2 to Less Than 12 Years Old With Hereditary Angioedema: Results From the Phase 3 SPRING Study.
    Maurer M; Lumry WR; Li HH; Aygören-Pürsün E; Busse PJ; Jacobs J; Nurse C; Ahmed MA; Watt M; Yu M;
    J Allergy Clin Immunol Pract; 2024 Jan; 12(1):201-211.e6. PubMed ID: 37730089
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Gene therapy for C1 esterase inhibitor deficiency in a Murine Model of Hereditary angioedema.
    Qiu T; Chiuchiolo MJ; Whaley AS; Russo AR; Sondhi D; Kaminsky SM; Crystal RG; Pagovich OE
    Allergy; 2019 Jun; 74(6):1081-1089. PubMed ID: 30059156
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Biological therapy in hereditary angioedema: transformation of a rare disease.
    Longhurst H; Farkas H
    Expert Opin Biol Ther; 2020 May; 20(5):493-501. PubMed ID: 31994957
    [No Abstract]   [Full Text] [Related]  

  • 49. Oral plasma kallikrein inhibitor BCX7353 for treatment of hereditary angioedema.
    Hwang JR; Hwang G; Johri A; Craig T
    Immunotherapy; 2019 Dec; 11(17):1439-1444. PubMed ID: 31635497
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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]  

  • 51. 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]  

  • 52. Berotralstat: First Approval.
    Lee A
    Drugs; 2021 Feb; 81(3):405-409. PubMed ID: 33646555
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Bradykinin-mediated diseases.
    Kaplan AP
    Chem Immunol Allergy; 2014; 100():140-7. PubMed ID: 24925394
    [TBL] [Abstract][Full Text] [Related]  

  • 54. C1-esterase inhibitor (Cinryze
    Gupta R; Balduzzi J; Davis-Lorton M
    Immunotherapy; 2018 Jun; 10(8):635-642. PubMed ID: 29569504
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Real-world changes in costs over time among patients in the United States with hereditary angioedema on long-term prophylaxis with lanadelumab.
    Shah CH; Princic N; Evans KA; Schultz BG
    J Med Econ; 2023; 26(1):871-877. PubMed ID: 37395381
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The real life experience goes on: update after 4 years on the first cohort treated with lanadelumab at our center.
    Buttgereit T; Vera Ayala C; Aykanat S; Weller K; Gutsche A; Maurer M; Magerl M
    Front Immunol; 2024; 15():1405317. PubMed ID: 38799421
    [TBL] [Abstract][Full Text] [Related]  

  • 57. C1-inhibitor polymers activate the FXII-dependent kallikrein-kinin system: Implication for a role in hereditary angioedema.
    Madsen DE; Sidelmann JJ; Biltoft D; Gram J; Hansen S
    Biochim Biophys Acta; 2015 Jun; 1850(6):1336-42. PubMed ID: 25800206
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Recent advances in the management of hereditary angioedema.
    Hemperly SE; Agarwal NS; Xu YY; Zhi YX; Craig TJ
    J Am Osteopath Assoc; 2013 Jul; 113(7):546-55. PubMed ID: 23843378
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Hereditary angiodema: a current state-of-the-art review, VI: novel therapies for hereditary angioedema.
    Frank MM
    Ann Allergy Asthma Immunol; 2008 Jan; 100(1 Suppl 2):S23-9. PubMed ID: 18220149
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 14.