BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

488 related articles for article (PubMed ID: 34956216)

  • 1. Angioedema Without Wheals: Challenges in Laboratorial Diagnosis.
    Grumach AS; Veronez CL; Csuka D; Farkas H
    Front Immunol; 2021; 12():785736. PubMed ID: 34956216
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels.
    Joseph K; Tholanikunnel BG; Wolf B; Bork K; Kaplan AP
    J Allergy Clin Immunol; 2016 Jun; 137(6):1822-1829.e1. PubMed ID: 26395818
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients.
    Mansi M; Zanichelli A; Coerezza A; Suffritti C; Wu MA; Vacchini R; Stieber C; Cichon S; Cicardi M
    J Intern Med; 2015 May; 277(5):585-93. PubMed ID: 25196353
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiency.
    Suffritti C; Zanichelli A; Maggioni L; Bonanni E; Cugno M; Cicardi M
    Clin Exp Allergy; 2014 Dec; 44(12):1503-14. PubMed ID: 24552232
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pathogenic mechanisms of bradykinin mediated diseases: dysregulation of an innate inflammatory pathway.
    Kaplan AP; Joseph K
    Adv Immunol; 2014; 121():41-89. PubMed ID: 24388213
    [TBL] [Abstract][Full Text] [Related]  

  • 7. sgp120 and the contact system in hereditary angioedema: A diagnostic tool in HAE with normal C1 inhibitor.
    Larrauri B; Hester CG; Jiang H; Miletic VD; Malbran A; Bork K; Kaplan A; Frank M
    Mol Immunol; 2020 Mar; 119():27-34. PubMed ID: 31955064
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Angioedema without urticaria: novel findings which must be measured in clinical setting.
    Veronez CL; Grumach AS
    Curr Opin Allergy Clin Immunol; 2020 Jun; 20(3):253-260. PubMed ID: 32073435
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Impaired control of the contact system in hereditary angioedema with normal C1-inhibitor.
    Bova M; Suffritti C; Bafunno V; Loffredo S; Cordisco G; Del Giacco S; De Pasquale TMA; Firinu D; Margaglione M; Montinaro V; Petraroli A; Radice A; Brussino L; Zanichelli A; Zoli A; Cicardi M
    Allergy; 2020 Jun; 75(6):1394-1403. PubMed ID: 31860755
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hereditary angioedema biological diagnosis].
    Ponard D
    Presse Med; 2015 Jan; 44(1):57-64. PubMed ID: 25511654
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biochemistry, molecular genetics, and clinical aspects of hereditary angioedema with and without C1 inhibitor deficiency.
    Miyata T; Horiuchi T
    Allergol Int; 2023 Jul; 72(3):375-384. PubMed ID: 37169642
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary and acquired angioedema.
    Patel G; Pongracic JA
    Allergy Asthma Proc; 2019 Nov; 40(6):441-445. PubMed ID: 31690390
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recurrent Angioedema: Occurrence, Features, and Concomitant Diseases in an Italian Single-Center Study.
    Triggianese P; Guarino MD; Pellicano C; Borzi M; Greco E; Modica S; De Carolis C; Perricone R
    Int Arch Allergy Immunol; 2017; 172(1):55-63. PubMed ID: 28222436
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Janus faces of acquired angioedema: C1-inhibitor deficiency, lymphoproliferation and autoimmunity.
    Wu MA; Castelli R
    Clin Chem Lab Med; 2016 Feb; 54(2):207-14. PubMed ID: 26068904
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymes.
    Joseph K; Bains S; Tholanikunnel BG; Bygum A; Aabom A; Koch C; Farkas H; Varga L; Ghebrehiwet B; Kaplan AP
    Allergy; 2015 Jan; 70(1):115-9. PubMed ID: 25186184
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Shortened Activated Partial Thromboplastin Time May Help in Diagnosing Hereditary and Acquired Angioedema.
    Bork K; Witzke G
    Int Arch Allergy Immunol; 2016; 170(2):101-7. PubMed ID: 27463190
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of patients with angioedema without wheals: the importance of F12 gene screening.
    Firinu D; Bafunno V; Vecchione G; Barca MP; Manconi PE; Santacroce R; Margaglione M; Del Giacco SR
    Clin Immunol; 2015 Apr; 157(2):239-48. PubMed ID: 25744496
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The importance of recognizing and managing a rare form of angioedema: hereditary angioedema due to C1-inhibitor deficiency.
    Jacobs J; Neeno T
    Postgrad Med; 2021 Aug; 133(6):639-650. PubMed ID: 33993830
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary angioedema: Pathophysiology (HAE type I, HAE type II, and HAE nC1-INH).
    Wedner HJ
    Allergy Asthma Proc; 2020 Nov; 41(Suppl 1):S14-S17. PubMed ID: 33109319
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.