These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


175 related items for PubMed ID: 3924818

  • 1. [Current diagnostic possibilities in hereditary angioedema and acquired angioedema].
    Dick W, Cullmann W.
    Immun Infekt; 1985 May; 13(3):113-8. PubMed ID: 3924818
    [Abstract] [Full Text] [Related]

  • 2. A new simple method for determination of C1-esterase inhibitor activity in plasma.
    Wiman B, Nilsson T.
    Clin Chim Acta; 1983 Mar 14; 128(2-3):359-66. PubMed ID: 6602012
    [Abstract] [Full Text] [Related]

  • 3. [New preparation method of C1 esterase for the dosage of its plasma inhibitor].
    Gozin D, Ollier-Hartmann MP, Lerable J, Hartmann L, Soulier JP.
    Biomed Pharmacother; 1983 Mar 14; 37(5):228-30. PubMed ID: 6607074
    [Abstract] [Full Text] [Related]

  • 4. Complement component analysis in angiodema. Diagnostic value.
    Brasher GW, Starr JC, Hall FF, Spiekerman AM.
    Arch Dermatol; 1975 Sep 14; 111(9):1140-2. PubMed ID: 1167046
    [Abstract] [Full Text] [Related]

  • 5. [A case of hereditary angioneurotic edema provoked by functional insufficiency of C1-inactivator].
    Didkovskiĭ NA, Paskhina TS, Rabinovich SE, Nartikova VF, Dvoretskiĭ LI.
    Ter Arkh; 1989 Sep 14; 61(6):116-9. PubMed ID: 2799695
    [Abstract] [Full Text] [Related]

  • 6. [Hereditary angioedema: description of a sibship and review].
    Matter L, Schopfer K, Voegelin HP, Fueter R.
    Schweiz Med Wochenschr; 1981 Aug 22; 111(34):1238-45. PubMed ID: 6974398
    [Abstract] [Full Text] [Related]

  • 7. [Hereditary angioedema by defict of C1 esterase. Our experience in 8 cases].
    Sastre Castillo A, Verea H, Lahoz F, Pérez Guerrero J, Vallejo J.
    Allergol Immunopathol (Madr); 1979 Aug 22; 7(2):141-6. PubMed ID: 313695
    [Abstract] [Full Text] [Related]

  • 8. [A case report of hereditary angioedema and studies on the serum components of complement, C1-inactivator and proteinase inhibitors during edema attack].
    Mikami A, Kohno M.
    Hokkaido Igaku Zasshi; 1987 May 22; 62(3):497-500. PubMed ID: 3610041
    [Abstract] [Full Text] [Related]

  • 9. A kinetic test for the assay of the C1 esterase-inhibitor.
    Schena FP, Manno C, D'Agostino R, Bruno G, Cramarossa F, Bonomo L.
    J Clin Chem Clin Biochem; 1980 Jan 22; 18(1):17-21. PubMed ID: 6965706
    [Abstract] [Full Text] [Related]

  • 10. [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 Jan 22; 53(1):21-5. PubMed ID: 9659739
    [Abstract] [Full Text] [Related]

  • 11. Hereditary angioneurotic edema: immunochemical 'activity' without clinical expression.
    Spitzer RE, Stitzel AE, Urmson JR.
    Int Arch Allergy Appl Immunol; 1980 Jan 22; 61(3):286-92. PubMed ID: 6965489
    [Abstract] [Full Text] [Related]

  • 12. [Hereditary angioedema].
    Zusserman MG, Reyes PA.
    Alergia; 1984 Jan 22; 31(1):7-11. PubMed ID: 6375439
    [No Abstract] [Full Text] [Related]

  • 13. [Activity of total complement and concentration of its components C1q, C3, C4 and C1-inactivator in cancer].
    Matoses Cuquerella S, O'Connor Miquel C, Lluch Hernández AM, García-Conde Bru J.
    Med Clin (Barc); 1988 Dec 10; 91(20):769-74. PubMed ID: 3266280
    [No Abstract] [Full Text] [Related]

  • 14. Electroimmunoassay of C1 inactivator and C4 in hereditary angioneurotic edema (HANE). A simplified diagnostic procedure.
    Laurell AB, Mårtensson U, Sjöholm A.
    Clin Immunol Immunopathol; 1976 May 10; 5(3):308-13. PubMed ID: 1277590
    [No Abstract] [Full Text] [Related]

  • 15. [Profile of the complement system in a family with hereditary angioedema].
    Rivero S, Guzmán L.
    Rev Med Chil; 1983 Nov 10; 111(11):1111-6. PubMed ID: 6431574
    [No Abstract] [Full Text] [Related]

  • 16. [Familial studies of patients with hereditary angioedema].
    Bozhkov B, Nikolov K, Baleva M.
    Vutr Boles; 1988 Nov 10; 27(4):62-5. PubMed ID: 3213025
    [Abstract] [Full Text] [Related]

  • 17. The C1 inhibitor deficiency. A review.
    Carreer FM.
    Eur J Clin Chem Clin Biochem; 1992 Dec 10; 30(12):793-807. PubMed ID: 1489854
    [Abstract] [Full Text] [Related]

  • 18. Unique C1 inhibitor dysfunction in a kindred without angioedema. I. A mutant C1 INH that inhibits C1-s but not C1-r.
    Wisnieski JJ, Knauss TC, Yike I, Dearborn DG, Narvy RL, Naff GB.
    J Immunol; 1994 Mar 15; 152(6):3199-209. PubMed ID: 8144914
    [Abstract] [Full Text] [Related]

  • 19. Distinction between hereditary and acquired angioneurotic oedema according to the complement system.
    Brecy H, Hartmann L.
    Biomedicine; 1975 Oct 20; 23(8):328-34. PubMed ID: 1231927
    [Abstract] [Full Text] [Related]

  • 20. [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 20; 43(5):413-7. PubMed ID: 1842037
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 9.