| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF01489349 |
| P698 | PubMed publication ID | 881774 |
| P2093 | author name string | K. Mueller | |
| F. R. Matthias | |||
| H. G. Lasch | |||
| W. H. Krause | |||
| S. Ganssert | |||
| P2860 | cites work | Fibrinogen Philadelphia. A hereditary hypodysfibrinogenemia characterized by fibrinogen hypercatabolism | Q34462314 |
| Fibrinogen St. Louis: a new inherited fibrinogen variant, coincidentally associated with hemophilia A. | Q34494312 | ||
| Fibrinogen Cleveland II. An abnormal fibrinogen with defective release of fibrinopeptide A. | Q34517341 | ||
| Studies on the structural abnormality of fibrinogen Paris I | Q35199051 | ||
| Congenital dysfibrinogenemia. Report on a new family (fibrinogen "Wiesbaden") | Q36507444 | ||
| Chromatographic, ultracentrifugal, and related studies of fibrinogen “Baltimore” | Q37710079 | ||
| Abnormal fibrinogens. A review | Q39933999 | ||
| Congenital and familial dysfibrinogenemia without hemorrhagic tendancy | Q44489598 | ||
| A new inherited coagulation disorder caused by an abnormal fibrinogen ('fibrinogen Baltimore'). | Q47717618 | ||
| Fibrinogen 'Leuven', another genetic variant | Q47841889 | ||
| A new congenital abnormality of human fibrinogen. Fibrinogen Bethesda II. | Q47937630 | ||
| Fibrinogen Montreal. A new case of congenital dysfibrinogenemia with defective aggregation of monomers | Q47937654 | ||
| Fibrinogen Troyes--fibrinogen Metz. Two new cases of congenital dysfibrinogenemia. | Q48032983 | ||
| Fibrinogen Detroit--a molecular defect in the N-terminal disulphide knot of human fibrinogen? | Q55061969 | ||
| Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (Paris I) | Q59086900 | ||
| Hypodysfibrinogenemia: fibrinogen giessen II (author's transl) | Q67276702 | ||
| Studies on chemically modified fibrinogen | Q67860427 | ||
| [A new case of Congenital and familial dysfibrinogenemia without Hemorrhagic Diathesis] | Q69965598 | ||
| [A new case of dysfibrinogenemia] | Q71803682 | ||
| Congenital disorders of fibrinogen | Q72552621 | ||
| [Congenital hypofibrinogenemia with fibrinoasthenia.] | Q78475788 | ||
| A quick and accurate method for the determination of fibronogen in plasma | Q78934157 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | German | Q188 |
| P921 | main subject | Dysfibrinogenemia | Q5319404 |
| P304 | page(s) | 539-543 | |
| P577 | publication date | 1977-06-01 | |
| P1433 | published in | Klinische Wochenschrift | Q27711855 |
| P478 | volume | 55 |
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