BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

270 related articles for article (PubMed ID: 6440668)

  • 1. [Hereditary angioneurotic edema: a molecular disease caused by a defect in the O-glycosylation of C1 esterase inhibitor (C1-INH)].
    Ollier-Hartmann MP; Strecker G; Montreuil J; Hartmann L
    C R Acad Sci III; 1984; 299(16):667-9. PubMed ID: 6440668
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary and acquired deficiencies of C1 inhibitor.
    Davis AE
    Immunodefic Rev; 1989; 1(3):207-26. PubMed ID: 2698641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Hereditary or acquired angioedema caused by functional deficiency of C1 inhibitor--a still unfamiliar disease picture].
    Wüthrich B; Devay J; Späth P
    Schweiz Med Wochenschr; 1999 Feb; 129(7):285-91. PubMed ID: 10093876
    [TBL] [Abstract][Full Text] [Related]  

  • 4. C1-inhibitor--biochemical properties and clinical applications.
    Al-Abdullah IH; Greally J
    Crit Rev Immunol; 1985; 5(4):317-30. PubMed ID: 3899511
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [New possibilities of treating acute angioedema caused by C1-inhibitor deficiency].
    Obtułowicz K; Głuszko P; Radwan J; Szczeklik A
    Pol Tyg Lek; 1989 Jul; 44(27):646-8. PubMed ID: 2637436
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. [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; 37(5):228-30. PubMed ID: 6607074
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [The course of acquired C 1 esterase inhibitor deficiency in lymphoproliferative syndrome].
    Benitah E; Wautier JL; Cohen F; Herman D
    Ann Med Interne (Paris); 1988; 139(7):488-90. PubMed ID: 3072895
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 338(1-2):14-20. PubMed ID: 18655790
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Angioedema due to acquired C1-esterase inhibitor deficiency in a patient with Helicobacter pylori infection.
    Farkas H; Gyeney L; Majthényi P; Füst G; Varga L
    Z Gastroenterol; 1999 Jun; 37(6):513-8. PubMed ID: 10427658
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A new type of acquired C1 inhibitor deficiency associated with systemic lupus erythematosus.
    Cacoub P; Frémeaux-Bacchi V; De Lacroix I; Guillien F; Kahn MF; Kazatchkine MD; Godeau P; Piette JC
    Arthritis Rheum; 2001 Aug; 44(8):1836-40. PubMed ID: 11508436
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Simultaneous occurrence of hereditary angioneurotic edema and Crohn disease].
    Farkas H; Gyeney L; Nemesánszky E; Káldi G; Kukán F; Masszi I; Soós J; Bély M; Farkas E; Füst G; Varga L
    Orv Hetil; 1998 May; 139(19):1165-9. PubMed ID: 9613166
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Anomaly of the polypeptide and oligosaccharide chains of alpha-2-neuraminoglycoprotein in various types of hereditary angioneurotic edema].
    Ollier-Hartmann MP; Hartmann L
    C R Seances Acad Sci D; 1980 May; 290(18):1201-4. PubMed ID: 6772326
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the C1 inhibitor gene that result in hereditary angioneurotic edema.
    Davis AE; Bissler JJ; Cicardi M
    Behring Inst Mitt; 1993 Dec; (93):313-20. PubMed ID: 8172583
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Acquired angioneurotic edema caused by acquired deficiency of C1 esterase inhibitor disclosing lymphoproliferative syndrome. Apropos of a case, review of the literature].
    Chevrant-Breton J; Mazéas D; Bagot M; Henry M; Goasguen J; Robin JP
    Ann Dermatol Venereol; 1982; 109(12):1049-56. PubMed ID: 7171202
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hereditary angioneurotic edema. Clinical aspects, pathogenesis and therapy].
    Schindera F; Rother U; Hufnagel C
    Helv Paediatr Acta; 1978 Aug; 33(3):259-66. PubMed ID: 711490
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Glomerulonephritis and hereditary angioedema: report of 2 cases.
    Hory B; Haultier JJ
    Clin Nephrol; 1989 May; 31(5):259-63. PubMed ID: 2736814
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.
    Cicardi M; Igarashi T; Rosen FS; Davis AE
    J Clin Invest; 1987 Mar; 79(3):698-702. PubMed ID: 3818946
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Plasma levels of C1- inhibitor complexes and cleaved C1- inhibitor in patients with hereditary angioneurotic edema.
    Cugno M; Nuijens J; Hack E; Eerenberg A; Frangi D; Agostoni A; Cicardi M
    J Clin Invest; 1990 Apr; 85(4):1215-20. PubMed ID: 2318974
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Respiratory manifestations in hereditary angioneurotic edema].
    Legendre M; Chiche JF; Molina C; Grouffal C; Betail G
    Rev Pneumol Clin; 1985; 41(4):251-8. PubMed ID: 4081477
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.