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 *

127 related articles for article (PubMed ID: 4939580)

  • 1. [Physiopathology and clinical picture of hereditary antiproteinase deficiency syndromes].
    Duck HJ
    Z Gesamte Inn Med; 1971 Jul; 26(14):445-51. PubMed ID: 4939580
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hereditary Quincke's edema: a disease caused by an anomaly of serum complement].
    Lagrue G; Lagrue R
    Acquis Med Recent; 1972; ():81-93. PubMed ID: 4667799
    [No Abstract]   [Full Text] [Related]  

  • 3. [Genetically determined pulmonary emphysema].
    Pawlikowski T
    Wiad Lek; 1973 Jul; 26(13):1223-6. PubMed ID: 4580739
    [No Abstract]   [Full Text] [Related]  

  • 4. [Hereditary deficiency of 1 -antitrypsin].
    Dautrevaux M
    Lille Med; 1971 Oct; 16(8):1113-21. PubMed ID: 5120783
    [No Abstract]   [Full Text] [Related]  

  • 5. [Hereditary complement deficiencies].
    Richard J
    Lille Med; 1971 Oct; 16(8):1125-53. PubMed ID: 5120785
    [No Abstract]   [Full Text] [Related]  

  • 6. Inherited abnormalities of the complement system in man.
    Ruddy S; Austen KF
    Prog Med Genet; 1970; 7():69-95. PubMed ID: 4911921
    [No Abstract]   [Full Text] [Related]  

  • 7. The pattern of inheritance of alpha 1 antitrypsin deficiency and associated pulmonary disease.
    Richardson RH; Guenter CA; Welch MH; Hyde RM; Hammarsten JF
    Am Rev Respir Dis; 1969 Nov; 100(5):619-25. PubMed ID: 4987089
    [No Abstract]   [Full Text] [Related]  

  • 8. [Studies on complement factors in hereditary Quincke's edema].
    Kueppers F; Schulz KH
    Arch Dermatol Forsch; 1972; 244():560-2. PubMed ID: 4648771
    [No Abstract]   [Full Text] [Related]  

  • 9. [Hereditary angioneurotic edema].
    Stoboeus N
    Lakartidningen; 1974 Jun; 71(23):2362. PubMed ID: 4839935
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hereditary angioneurotic edema. Biochemical and genetic study of 5 families].
    Brécy H; Rethore MO; Hartmann L
    Ann Biol Clin (Paris); 1971; 29(5):351-60. PubMed ID: 5145636
    [No Abstract]   [Full Text] [Related]  

  • 11. Specificity of inhibitors lacking in alpha antitrypsin deficiency and hereditary angioedema toward human proteolytic enzymes.
    Colman RW; Mitchell B
    Clin Chim Acta; 1972 Jun; 39(1):5-14. PubMed ID: 4261035
    [No Abstract]   [Full Text] [Related]  

  • 12. [Respiratory pathology and hereditary alpha1 antitrypsin deficiency].
    Lemercier JP; Ropartz C; Langlois A; Ourdas N; Desseauve J
    Presse Med (1893); 1969 May; 77(27):967-70. PubMed ID: 5795144
    [No Abstract]   [Full Text] [Related]  

  • 13. [Familial deficiency on alpha-1-antitrypsin].
    Wehinger H; Karitzky D; Witt I
    Z Kinderheilkd; 1971; 110(2):115-27. PubMed ID: 5580606
    [No Abstract]   [Full Text] [Related]  

  • 14. [Hereditary deficiency of complement in humans and animals].
    Pozsgi N
    Microbiol Parazitol Epidemiol (Bucur); 1971; 16(6):481-90. PubMed ID: 5134752
    [No Abstract]   [Full Text] [Related]  

  • 15. Alpha-1-antitrypsin deficiency: a defect in protein synthesis.
    Kueppers F; Fallat RJ
    Clin Chim Acta; 1969 Jun; 24(3):401-3. PubMed ID: 5790322
    [No Abstract]   [Full Text] [Related]  

  • 16. Inherited high serum levels of a functionally deficient complement esterase inhibitor associated with hereditary angioedema.
    Kueppers F; Berendes U; Schöpf E
    Humangenetik; 1972; 15(2):119-25. PubMed ID: 4626030
    [No Abstract]   [Full Text] [Related]  

  • 17. [Proteolytic and antitrypsinolytic activity and the state of the serum proteins in severe burns].
    Klimov IA; Sorokin AV
    Lab Delo; 1973; 4():226-7. PubMed ID: 4125475
    [No Abstract]   [Full Text] [Related]  

  • 18. The proteinase inhibitor deficiency syndromes.
    Alper CA
    Rev Allergy; 1971 Oct; 25(10):1015-7. PubMed ID: 5110797
    [No Abstract]   [Full Text] [Related]  

  • 19. [A molecular disease: hereditary angioneurotic edema. Study of 16 families].
    Hartmann L; Brécy H; Ollier MP; Rethore O
    Biomedicine; 1974 Jul; 21(7):294-302. PubMed ID: 4215470
    [No Abstract]   [Full Text] [Related]  

  • 20. Distribution and elimination of exogenous alpha1-antitrypsin.
    Makino S; Reed CE
    J Lab Clin Med; 1970 May; 75(5):742-6. PubMed ID: 4985792
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.