151 related articles for article (PubMed ID: 5741359)
1. [2 new forms of combined hereditary hemorrhagic diatheses].
Barkagan ZS; Sukhoveeva EIa; Shevchenko VI; Plavinskaia NIa
Ter Arkh; 1968 Oct; 40(10):45-51. PubMed ID: 5741359
[No Abstract] [Full Text] [Related]
2. [Congenital factor XIII deficiency: studies in an infant and his family].
Mertner MF
Monatsschr Kinderheilkd (1902); 1972 Jan; 120(1):28-31. PubMed ID: 5016722
[No Abstract] [Full Text] [Related]
3. Congenital hemorrhagic diathesis with deficiency of factor XIII. A case report and a family study.
Abels J; Sibinga CT; Meyler L
Thromb Diath Haemorrh; 1970 May; 23(2):340-6. PubMed ID: 5426214
[No Abstract] [Full Text] [Related]
4. [Hemorrhagic syndrome conditioned by inborn deficiency of coagulation factor XIII and report of the 2d case found in Yugoslavia].
Stanulović D; Popović K; Lucić A
Med Pregl; 1969; 22(5-6):243-7. PubMed ID: 5377250
[No Abstract] [Full Text] [Related]
5. Congenital factor XIII deficiency. Report of 2 cases.
Fradera J; Haddock J; Pérez-Santiago E; Maldonado N
Bol Asoc Med P R; 1969 Aug; 61(8):294-9. PubMed ID: 5271545
[No Abstract] [Full Text] [Related]
6. [Diagnostics and therapy of hemolytic-hemorrhagic transfusion incidents].
Brüster H
Zentralbl Neurochir; 1972; 33(1):63-8. PubMed ID: 5072151
[No Abstract] [Full Text] [Related]
7. [Hereditary deficiency in factor XIII activity-synthesis of a non-functional protein].
Duckert F
Schweiz Med Wochenschr; 1970 Feb; 100(7):328. PubMed ID: 4984094
[No Abstract] [Full Text] [Related]
8. [Hemorrhagic diathesis caused by a deficiency of the fibrin-stabilizing factor (factor 13)].
Lechler E; Köhler J
Verh Dtsch Ges Inn Med; 1968; 74():144-7. PubMed ID: 5714300
[No Abstract] [Full Text] [Related]
9. Kaolin partial thromboplastin time: high levels of procoagulants producing short clotting times or masking deficiencies of other procoagulants or low concentrations of anticoagulants.
Edson JR; Krivit W; White JG
J Lab Clin Med; 1967 Sep; 70(3):463-70. PubMed ID: 6072020
[No Abstract] [Full Text] [Related]
10. [Congenital deficiency of fibrin stabilizing activity. Presence of a protein immunologically analogous to factor XIII].
Aguercif M; Nigg OM; Lopez JM; Bouvier CA
Nouv Rev Fr Hematol; 1971; 11(6):841-8. PubMed ID: 4261156
[No Abstract] [Full Text] [Related]
11. [Congenital hereditary coagulopathy. Part 1: Classification, diagnosis].
Neidhardt B
Fortschr Med; 1975 Nov; 93(32):1582-5. PubMed ID: 1220998
[No Abstract] [Full Text] [Related]
12. [Clinical laboratory characteristics of the severe form of hereditary fibrin-stabilizing factor (factor XIII) deficiency].
Barkagan LZ; Arkhipov BF
Probl Gematol Pereliv Krovi; 1980 Aug; 25(8):54-8. PubMed ID: 7413627
[No Abstract] [Full Text] [Related]
13. Inherited fibrinolytic hyperactivity.
Self J; Matthews C
Arch Intern Med; 1968 Oct; 122(4):357-8. PubMed ID: 5676420
[No Abstract] [Full Text] [Related]
14. [Clinical experience in the hemorrhagic disease (1964-1969)].
Baudo F; Ghessi A; De Cataldo F
Minerva Med; 1971 Jun; 62(50):2533-7. PubMed ID: 5572158
[No Abstract] [Full Text] [Related]
15. [Hemorrhagic diatheses caused by coagulation factor deficit and by primary hyperfibrinolysis].
Abbadessa V; Cuccio G
Minerva Anestesiol; 1980 Jul; 46(7):787-90. PubMed ID: 7242952
[No Abstract] [Full Text] [Related]
16. [Congenital deficiency of fibrin stabilizing factor (factor XIII)].
Barbui T; Di Luzio V
G Clin Med; 1968 Jun; 49(6):646-61. PubMed ID: 4907419
[No Abstract] [Full Text] [Related]
17. [Stage diagnosis of hemorrhagic diatheses].
Lechner K
Internist (Berl); 1985 Mar; 26(3):141-6. PubMed ID: 3886582
[No Abstract] [Full Text] [Related]
18. [The partial thromboplastin test in the preoperative "screening" of hemorrhagic patients].
Bracali G; Niccoli Vallesi R; Rubertelli M
Ann Laringol Otol Rinol Faringol; 1967; 66(3):333-7. PubMed ID: 5632636
[No Abstract] [Full Text] [Related]
19. [Hemorrhagic syndrome conditioned by congenital deficiency of factor XIII. On the occasion of the first case discovered in Yugoslavia].
Rolović Z; Berović R
Srp Arh Celok Lek; 1968 Jun; 96(6):593-602. PubMed ID: 5192188
[No Abstract] [Full Text] [Related]
20. Congenital factor XIII deficiency and increased fibrinolysis. A case report.
Hathirat P; Jamieson BA; Beatty EC
Rocky Mt Med J; 1970 Jun; 67(6):39-42. PubMed ID: 5431447
[No Abstract] [Full Text] [Related]
[Next] [New Search]
