BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 5698343)

  • 1. [Familial study in congenital Hageman factor deficiency (blood coagulation factor XII)].
    Baumann R; Straub PW
    Schweiz Med Wochenschr; 1968 Oct; 98(42):1653-5. PubMed ID: 5698343
    [No Abstract]   [Full Text] [Related]  

  • 2. Congenital deficiency of Hageman factor (clotting factor XII). Report on the first two families found in Switzerland.
    Baumann R; Straub PW
    Helv Med Acta; 1968 Nov; 34(4):313-26. PubMed ID: 5704616
    [No Abstract]   [Full Text] [Related]  

  • 3. [Study of a family with factor XII deficiency].
    Licenziati M; Lazzari R; Falsina A
    Minerva Med; 1975 Feb; 66(11):511-3. PubMed ID: 234603
    [No Abstract]   [Full Text] [Related]  

  • 4. [Hageman factor deficiency (factor XII)--hemorrhage or thrombosis?].
    Schott G; Lutze G
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1985; 112(3):436-41. PubMed ID: 2414173
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital deficiency of factor 13: report of a family from Newfoundland with associated mild deficiency of factor XII.
    Hanna M
    Pediatrics; 1970 Oct; 46(4):611-9. PubMed ID: 5503696
    [No Abstract]   [Full Text] [Related]  

  • 6. New families with factor XII deficiency.
    Egeberg O
    Thromb Diath Haemorrh; 1970 Jun; 23(3):441-8. PubMed ID: 5432189
    [No Abstract]   [Full Text] [Related]  

  • 7. [Factor XII deficiency in two brothers].
    Müller G; Hilgard P; Hiemeyer V
    Dtsch Med Wochenschr; 1973 Feb; 98(6):267-9. PubMed ID: 4684650
    [No Abstract]   [Full Text] [Related]  

  • 8. [Hemorrhagic diathesis associated with partial factor XII deficiency].
    Zywicka-Lopaciuk H; Lopaciuk S
    Acta Haematol Pol; 1972; 3(3):257-63. PubMed ID: 4649309
    [No Abstract]   [Full Text] [Related]  

  • 9. Brief recordings. Rheumatoid arthritis in a patient with Hageman trait.
    Donaldson VH; Glueck HI; Fleming T
    N Engl J Med; 1972 Mar; 286(10):528-30. PubMed ID: 5059265
    [No Abstract]   [Full Text] [Related]  

  • 10. Factor-XII congenital deficiency. A new family study.
    Lucia JF; Ercoreca L; Torres M; Giralt M; Raichs A
    Thromb Haemost; 1979 Oct; 42(3):1009-17. PubMed ID: 505391
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Factor XII defect and hemorrhage. Evidence for a new type of hereditary hemostatic disorder.
    Egeberg O
    Thromb Diath Haemorrh; 1970 Jun; 23(3):432-40. PubMed ID: 5432188
    [No Abstract]   [Full Text] [Related]  

  • 12. A new family with congenital factor XII deficiency.
    Barbui T; Dini E
    Acta Haematol; 1975; 54(6):345-9. PubMed ID: 812321
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Feline factor XII (Hageman) deficiency.
    Green RA; White F
    Am J Vet Res; 1977 Jun; 38(6):893-5. PubMed ID: 879587
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The enigma of severe factor XI deficiency without hemmorrhagic symptoms. Distinction from Hageman factor and "Fletcher factor" deficiency; family study; and problems of diagnosis.
    Edson JR; White JG; Krivit W
    Thromb Diath Haemorrh; 1967 Dec; 18(3-4):342-8. PubMed ID: 5590232
    [No Abstract]   [Full Text] [Related]  

  • 15. Hageman trait. The first case in Hungary (brief report).
    Elödi S; Mód A; Poros A
    Haematologia (Budap); 1971; 5(4):459-60. PubMed ID: 5148970
    [No Abstract]   [Full Text] [Related]  

  • 16. [Hageman factor deficiency. Apropos of a case].
    Aznar J; Mayans J; Aznar JA; Fernández-Pavón A; Calabuig R
    Sangre (Barc); 1973; 18(3):356-64. PubMed ID: 4757644
    [No Abstract]   [Full Text] [Related]  

  • 17. Hageman trait (factor XII deficiency): a probably second genotype inherited as an autosomal dominant characteristic.
    Bennett B; Ratnoff OD; Holt JB; Roberts HR
    Blood; 1972 Sep; 40(3):412-5. PubMed ID: 4626869
    [No Abstract]   [Full Text] [Related]  

  • 18. [Hageman factor deficiency: second case found in Japanese].
    Miwa S; Asai I; Tsukada T; Shimizu M; Teramura K
    Nihon Ketsueki Gakkai Zasshi; 1967 Nov; 30(6):859-63. PubMed ID: 5627222
    [No Abstract]   [Full Text] [Related]  

  • 19. [Use of chromogenic substrates in the clarification of disorders in the early stages of blood coagulation].
    Vogel G; Stürzebecher J; Klessen C; Lauten G
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1982; 109(1):115-20. PubMed ID: 6177592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Coagulation disorder caused by Hageman factor (factor XII) deficiency. (First case in Italy)].
    Girolami A; Scarpa R; Lazzarini M; Brunetti A
    Riv Crit Clin Med; 1968; 68(3):265-78. PubMed ID: 5737878
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.