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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 8430403)

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

  • 2. [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; 53(1):21-5. PubMed ID: 9659739
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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; 82(1):29-30. PubMed ID: 2028073
    [No Abstract]   [Full Text] [Related]  

  • 4. [Investigation of the complement system in clinical practice].
    Frémeaux-Bacchi V; Dragon-Durey MA; Blouin J; Mouthon L; Fridman WH
    Ann Med Interne (Paris); 2003 Dec; 154(8):529-40. PubMed ID: 15037829
    [TBL] [Abstract][Full Text] [Related]  

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

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

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

  • 8. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Utilization of complement testing in clinical medicine.
    Abdul-Aziz K; Faizal AA
    Saudi Med J; 2006 Nov; 27(11):1775-7. PubMed ID: 17106567
    [No Abstract]   [Full Text] [Related]  

  • 10. [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]  

  • 11. Chronic urticaria.
    Zauli D; Deleonardi G; Grassi A; Bortolotti R; Lari F; Ballardini G; Bianchi FB
    Arch Dermatol; 2001 Apr; 137(4):504-5. PubMed ID: 11295939
    [No Abstract]   [Full Text] [Related]  

  • 12. [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; 91(20):769-74. PubMed ID: 3266280
    [No Abstract]   [Full Text] [Related]  

  • 13. Melkersson-Rosenthal syndrome and acquired C1 inhibitor deficiency.
    Masson F; Barete S; Frémeaux-Bacchi V; Szpirglas H; Agbo-Godeau S; Chosidow O; Piette JC; Francès C
    Dermatology; 2008; 217(2):114-20. PubMed ID: 18477847
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Acquired angioedema and hypocompleentemia in a patient with myelofibrosis. Effect of danazol treatment.
    Nilsen A; Matre R
    Acta Med Scand; 1980; 207(1-2):123-5. PubMed ID: 6899952
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. C1-INH and C3/C4 levels do not correlate with long-term danazole dosage and HAE-1 attack-free interval.
    Schneider LA; Maetzke J; Staib G; Scharffetter-Kochanek K
    Allergy; 2005 Sep; 60(9):1214-5. PubMed ID: 16076313
    [No Abstract]   [Full Text] [Related]  

  • 18. Which complement assays and typings are necessary for the diagnosis of complement deficiency in patients with lupus erythematosus? A study of 25 patients.
    Boeckler P; Meyer A; Uring-Lambert B; Goetz J; Cribier B; Hauptmann G; Lipsker D
    Clin Immunol; 2006 Nov; 121(2):198-202. PubMed ID: 16987709
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Immunologic parameters in chronic urticaria].
    Malet A; Engel P; Huguet J; García-Calderón PA
    Allergol Immunopathol (Madr); 1986; 14(5):375-81. PubMed ID: 3799406
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hereditary complement deficiencies].
    Fischer E
    Hautarzt; 1982 Feb; 33(2):65-72. PubMed ID: 6281215
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.