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Journal Abstract Search

199 related items for PubMed ID: 15953110

  • 1. C1 inhibitor deficiency: diagnosis.
    Gompels MM, Lock RJ.
    Clin Exp Dermatol; 2005 Jul; 30(4):460-2. PubMed ID: 15953110
    [Abstract] [Full Text] [Related]

  • 2. [Hereditary angioedema, a rare cause of recurrent abdominal pains. A report of 2 clinical cases and comments of a general nature].
    Parisi G, Chiarelli A, Squadrone NP, Galante E.
    Minerva Pediatr; 1991 May; 43(5):413-7. PubMed ID: 1842037
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary angioedema C1 inhibitor deficiency].
    Fain O.
    Rev Prat; 2007 Mar 31; 57(6):591. PubMed ID: 17593781
    [No Abstract] [Full Text] [Related]

  • 4. A case of angioedema due to acquired C1 esterase inhibitor deficiency masquerading as suspected peritonitis: a case report.
    Hong SB, Kim CW, Kim JH, Kim JS, Han SB.
    J Emerg Med; 2011 Nov 31; 41(5):e99-e101. PubMed ID: 18486406
    [Abstract] [Full Text] [Related]

  • 5. [Hereditary angioneurotic Quincke's edema].
    Göring HD.
    Dermatol Monatsschr; 1985 Nov 31; 171(6):353-9. PubMed ID: 3926548
    [No Abstract] [Full Text] [Related]

  • 6. [Hereditary angioneurotic edema (its pathogenesis, clinical aspects, diagnosis, treatment)].
    Poroshina IuA, Androsov VN, Martynova VA.
    Ter Arkh; 1985 Nov 31; 57(4):119-21. PubMed ID: 4012617
    [No Abstract] [Full Text] [Related]

  • 7. [Familial studies of patients with hereditary angioedema].
    Bozhkov B, Nikolov K, Baleva M.
    Vutr Boles; 1988 Nov 31; 27(4):62-5. PubMed ID: 3213025
    [Abstract] [Full Text] [Related]

  • 8. Angioedema presenting as chronic gastrointestinal symptoms.
    Eck SL, Morse JH, Janssen DA, Emerson SG, Markovitz DM.
    Am J Gastroenterol; 1993 Mar 31; 88(3):436-9. PubMed ID: 8438855
    [Abstract] [Full Text] [Related]

  • 9. [Determination of complement proteins in the umbilical cord in the early diagnosis of hereditary angioneurotic edema].
    Ferlazzo B, Barrile A, Crisafi A, Quattrocchi P, Bonanno D, Giacobbe G, Sorge R.
    Recenti Prog Med; 1991 Jan 31; 82(1):29-30. PubMed ID: 2028073
    [No Abstract] [Full Text] [Related]

  • 10. C1 INH deficiency and angioedema: a spectrum of disease. Part two.
    Metzger WJ, Grem J, Halverson PC, Sharath MD, Shulan DJ, Lawton W, Weiler JM.
    Ann Allergy; 1984 Apr 31; 52(4):285-90. PubMed ID: 6711917
    [No Abstract] [Full Text] [Related]

  • 11. Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.
    Wagenaar-Bos IG, Drouet C, Aygören-Pursun E, Bork K, Bucher C, Bygum A, Farkas H, Fust G, Gregorek H, Hack CE, Hickey A, Joller-Jemelka HI, Kapusta M, Kreuz W, Longhurst H, Lopez-Trascasa M, Madalinski K, Naskalski J, Nieuwenhuys E, Ponard D, Truedsson L, Varga L, Nielsen EW, Wagner E, Zingale L, Cicardi M, van Ham SM.
    J Immunol Methods; 2008 Sep 30; 338(1-2):14-20. PubMed ID: 18655790
    [Abstract] [Full Text] [Related]

  • 12. [Profile of the complement system in a family with hereditary angioedema].
    Rivero S, Guzmán L.
    Rev Med Chil; 1983 Nov 30; 111(11):1111-6. PubMed ID: 6431574
    [No Abstract] [Full Text] [Related]

  • 13. Management of hereditary angioedema: a Canadian approach.
    Bowen T, Hebert J, Ritchie B, Burnham J, MacSween M, Warrington R, Yang W, Issekutz A, Karitsiotis N, McCombie N, Giulivi T.
    Transfus Apher Sci; 2003 Dec 30; 29(3):205-14. PubMed ID: 14572811
    [Abstract] [Full Text] [Related]

  • 14. C1 inhibitor deficiency: management.
    Gompels MM, Lock RJ, Advisory Group.
    Clin Exp Dermatol; 2005 Nov 30; 30(6):737-40. PubMed ID: 16197414
    [Abstract] [Full Text] [Related]

  • 15. [Hereditary angioedema due to C1-esterase inhibitor deficiency].
    Zeană C.
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Med Interna; 1989 Nov 30; 41(5):467-71. PubMed ID: 2575278
    [Abstract] [Full Text] [Related]

  • 16. C1 esterase inhibitor deficiency: three presentations.
    Baldwin J, Pence HL, Karibo JM, Massey EN.
    Ann Allergy; 1991 Aug 30; 67(2 Pt 1):107-13. PubMed ID: 1867444
    [Abstract] [Full Text] [Related]

  • 17. A multicentre evaluation of the diagnostic efficiency of serological investigations for C1 inhibitor deficiency.
    Gompels MM, Lock RJ, Morgan JE, Osborne J, Brown A, Virgo PF.
    J Clin Pathol; 2002 Feb 30; 55(2):145-7. PubMed ID: 11865013
    [Abstract] [Full Text] [Related]

  • 18. [Hereditary angioedema: clinical and laboratory aspects of 7 cases].
    Moschione-Castro AP, Croce J, Diogo CL, Jacob CM, Pastorino AC, Kirschfink M, Grumach AS.
    Rev Hosp Clin Fac Med Sao Paulo; 1998 Feb 30; 53(1):21-5. PubMed ID: 9659739
    [Abstract] [Full Text] [Related]

  • 19. [Deficiencies of C1 inhibitor: hereditary and acquired angioedema].
    Porcel-Pérez JM, López-Trascasa M.
    Rev Clin Esp; 1996 Mar 30; 196 Spec No():26-30. PubMed ID: 9206804
    [No Abstract] [Full Text] [Related]

  • 20. [Complement analysis tests].
    Mollnes TE, Nielsen EW, Høgåsen K, Mellbye OJ.
    Tidsskr Nor Laegeforen; 1993 Jan 20; 113(2):211-3. PubMed ID: 8430403
    [Abstract] [Full Text] [Related]

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