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Journal Abstract Search

487 related items for PubMed ID: 33442779

  • 1. Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene.
    Sharma J, Jindal AK, Banday AZ, Kaur A, Rawat A, Singh S, Longhurst H.
    Clin Rev Allergy Immunol; 2021 Jun; 60(3):305-315. PubMed ID: 33442779
    [Abstract] [Full Text] [Related]

  • 2. Definition and classification of hereditary angioedema.
    Proper SP, Lavery WJ, Bernstein JA.
    Allergy Asthma Proc; 2020 Nov 01; 41(Suppl 1):S03-S07. PubMed ID: 33109317
    [Abstract] [Full Text] [Related]

  • 3. 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 01; 40(3):814-827. PubMed ID: 36609679
    [Abstract] [Full Text] [Related]

  • 4. Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.
    Bork K, Machnig T, Wulff K, Witzke G, Prusty S, Hardt J.
    Orphanet J Rare Dis; 2020 Oct 15; 15(1):289. PubMed ID: 33059692
    [Abstract] [Full Text] [Related]

  • 5. Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.
    Bork K, Wulff K, Witzke G, Hardt J.
    Allergy; 2015 Aug 15; 70(8):1004-12. PubMed ID: 25952149
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 50(3):269-276. PubMed ID: 29513108
    [Abstract] [Full Text] [Related]

  • 7. Screening for Plasminogen Mutations in Hereditary Angioedema Patients.
    Farkas H, Dóczy A, Szabó E, Varga L, Csuka D.
    Genes (Basel); 2021 Mar 11; 12(3):. PubMed ID: 33799813
    [Abstract] [Full Text] [Related]

  • 8. The Expanding Spectrum of Mutations in Hereditary Angioedema.
    Veronez CL, Csuka D, Sheikh FR, Zuraw BL, Farkas H, Bork K.
    J Allergy Clin Immunol Pract; 2021 Jun 11; 9(6):2229-2234. PubMed ID: 33746090
    [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 11; 75(6):1394-1403. PubMed ID: 31860755
    [Abstract] [Full Text] [Related]

  • 10. The Genetics of Hereditary Angioedema: A Review.
    Santacroce R, D'Andrea G, Maffione AB, Margaglione M, d'Apolito M.
    J Clin Med; 2021 May 09; 10(9):. PubMed ID: 34065094
    [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 09; 72(3):375-384. PubMed ID: 37169642
    [Abstract] [Full Text] [Related]

  • 12. 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 Jul 09; 166(2):114-20. PubMed ID: 25790805
    [Abstract] [Full Text] [Related]

  • 13. Genetics of Hereditary Angioedema Revisited.
    Germenis AE, Speletas M.
    Clin Rev Allergy Immunol; 2016 Oct 09; 51(2):170-82. PubMed ID: 27116602
    [Abstract] [Full Text] [Related]

  • 14. Hereditary angioedema with normal C1-inhibitor: Clinical and genetic characterization of 15 Portuguese unrelated families.
    Dias de Castro E, Pinhal AL, Bragança M, Parente Freixo J, Martinho A.
    Ann Allergy Asthma Immunol; 2024 Jun 09; 132(6):730-736. PubMed ID: 38342132
    [Abstract] [Full Text] [Related]

  • 15. 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 09; 277(5):585-93. PubMed ID: 25196353
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 919():148496. PubMed ID: 38679185
    [Abstract] [Full Text] [Related]

  • 17. Hereditary and acquired angioedema.
    Patel G, Pongracic JA.
    Allergy Asthma Proc; 2019 Nov 01; 40(6):441-445. PubMed ID: 31690390
    [Abstract] [Full Text] [Related]

  • 18. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.
    Zeerleder S, Levi M.
    Ann Med; 2016 Nov 01; 48(4):256-67. PubMed ID: 27018196
    [Abstract] [Full Text] [Related]

  • 19. A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.
    Vatsiou S, Zamanakou M, Loules G, Psarros F, Parsopoulou F, Csuka D, Valerieva A, Staevska M, Porebski G, Obtulowicz K, Magerl M, Maurer M, Speletas M, Farkas H, Germenis AE.
    Allergol Int; 2020 Jul 01; 69(3):443-449. PubMed ID: 31959500
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 18(3):215-223. PubMed ID: 32065705
    [Abstract] [Full Text] [Related]

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