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Journal Abstract Search

142 related items for PubMed ID: 20864152

  • 1. A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation.
    López-Lera A, Favier B, de la Cruz RM, Garrido S, Drouet C, López-Trascasa M.
    J Allergy Clin Immunol; 2010 Dec; 126(6):1307-10.e3. PubMed ID: 20864152
    [No Abstract] [Full Text] [Related]

  • 2. Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency.
    Bygum A, Fagerberg CR, Ponard D, Monnier N, Lunardi J, Drouet C.
    Allergy; 2011 Jan; 66(1):76-84. PubMed ID: 20804470
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary angioedema--pathophysiology, genetics, symptoms].
    Muszyńska A, Janocha E, Fal AM.
    Pol Merkur Lekarski; 2008 Jul; 25(145):90-3. PubMed ID: 18839624
    [Abstract] [Full Text] [Related]

  • 4. Treatment of episodes of hereditary angioedema with C1 inhibitor: serial assessment of observed abnormalities of the plasma bradykinin-forming pathway and fibrinolysis.
    Joseph K, Tholanikunnel TE, Kaplan AP.
    Ann Allergy Asthma Immunol; 2010 Jan; 104(1):50-4. PubMed ID: 20143645
    [Abstract] [Full Text] [Related]

  • 5. Kinin formation in C1 inhibitor deficiency.
    Kaplan AP, Joseph K.
    J Allergy Clin Immunol; 2010 Jun; 125(6):1411-2; author reply 1412. PubMed ID: 20381848
    [No Abstract] [Full Text] [Related]

  • 6. First case of homozygous C1 inhibitor deficiency.
    Blanch A, Roche O, Urrutia I, Gamboa P, Fontán G, López-Trascasa M.
    J Allergy Clin Immunol; 2006 Dec; 118(6):1330-5. PubMed ID: 17137866
    [Abstract] [Full Text] [Related]

  • 7. [Bradykinin angioedemas].
    Du-Thanh A, Raison-Peyron N, Guillot B.
    Ann Dermatol Venereol; 2011 Dec; 138(4):328-35; quiz 327, 336. PubMed ID: 21497264
    [No Abstract] [Full Text] [Related]

  • 8. Evidence of impaired sense of smell in hereditary angioedema.
    Perricone C, Agmon-Levin N, Shoenfeld N, de Carolis C, Guarino MD, Gigliucci G, Milana I, Novelli L, Valesini G, Perricone R, Shoenfeld Y.
    Allergy; 2011 Jan; 66(1):149-54. PubMed ID: 20649895
    [Abstract] [Full Text] [Related]

  • 9. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor.
    Bork K, Wulff K, Meinke P, Wagner N, Hardt J, Witzke G.
    Clin Immunol; 2011 Oct; 141(1):31-5. PubMed ID: 21849258
    [Abstract] [Full Text] [Related]

  • 10. Hereditary angioedema and chronic urticaria: is there a possible association?
    Jorge AS, Dortas SD, Valle SO, França AT.
    J Investig Allergol Clin Immunol; 2009 Oct; 19(4):327-8. PubMed ID: 19639735
    [No Abstract] [Full Text] [Related]

  • 11. 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 Oct; 178(1):50-59. PubMed ID: 30278448
    [Abstract] [Full Text] [Related]

  • 12. Enzymatic pathways in the pathogenesis of hereditary angioedema: the role of C1 inhibitor therapy.
    Kaplan AP.
    J Allergy Clin Immunol; 2010 Nov; 126(5):918-25. PubMed ID: 20889195
    [Abstract] [Full Text] [Related]

  • 13. Disseminated tuberculosis in a patient with hereditary C1-inhibitor deficiency.
    Kallel-Sellami M, Blouin J, Abdelmalek R, Laadhar L, Zerzeri Y, Barbouche MR, Tiouiri H, Chaabène T, Fremeaux-Bacchi V, Zitouni M, Makni S.
    Infection; 2008 Mar; 36(2):181-3. PubMed ID: 18165858
    [No Abstract] [Full Text] [Related]

  • 14. Hereditary angioedema with normal C1 inhibitor.
    Bork K.
    Immunol Allergy Clin North Am; 2013 Nov; 33(4):457-70. PubMed ID: 24176211
    [Abstract] [Full Text] [Related]

  • 15. New hope for those with hereditary angioedema.
    Pepe J, Bielory L.
    Nursing; 2012 Apr; 42(4):43-6. PubMed ID: 22456213
    [No Abstract] [Full Text] [Related]

  • 16. The bradykinin-forming cascade and its role in hereditary angioedema.
    Kaplan AP, Joseph K.
    Ann Allergy Asthma Immunol; 2010 Mar; 104(3):193-204. PubMed ID: 20377108
    [Abstract] [Full Text] [Related]

  • 17. A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene.
    Büyüköztürk S, Eroğlu BK, Gelincik A, Uzümcü A, Ozşeker F, Colakoğlu B, Dal M, Uyguner ZO.
    J Allergy Clin Immunol; 2009 Apr; 123(4):962-4. PubMed ID: 19201015
    [No Abstract] [Full Text] [Related]

  • 18. Home treatment of hereditary angioedema with icatibant administered by health care professionals.
    Farkas H, Csuka D, Zotter Z, Varga L, Böröcz Z, Temesszentandrási G, Jakab L, Karádi I.
    J Allergy Clin Immunol; 2012 Mar; 129(3):851-852.e2. PubMed ID: 22154383
    [No Abstract] [Full Text] [Related]

  • 19. A novel C1 inhibitor gene mutation in a family with hereditary angioedema: Use of genetic analysis to facilitate early diagnosis.
    Yokoyama K, Horiuchi T, Hashimura C, Yoshida A.
    Allergol Int; 2020 Jan; 69(1):148-149. PubMed ID: 31409531
    [No Abstract] [Full Text] [Related]

  • 20. Molecular diagnosis and management of hereditary angioedema in a Greek family.
    Papadopoulou-Alataki E, Foerster T, Antari V, Pavlitou-Tsiontsi A, Varlamis G.
    Int Arch Allergy Immunol; 2008 Jan; 147(2):166-70. PubMed ID: 18535392
    [Abstract] [Full Text] [Related]

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