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23. Electroimmunoassay of plasma subunits-a and -s in a case of congenital fibrin stabilizing factor deficiency. Barbui T; Cartei G; Chisesi T; Dini E Thromb Diath Haemorrh; 1974 Sep; 32(1):124-31. PubMed ID: 4454035 [TBL] [Abstract][Full Text] [Related]
24. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations. Katona É; Muszbek L; Devreese K; Kovács KB; Bereczky Z; Jonkers M; Shemirani AH; Mondelaers V; Ermens AA Haemophilia; 2014 Jan; 20(1):114-20. PubMed ID: 24118344 [TBL] [Abstract][Full Text] [Related]
25. Congenital factor XIII deficiency. Prakash S; Kela K; Gopal R J Assoc Physicians India; 1981 Jun; 29(6):475-9. PubMed ID: 7320002 [No Abstract] [Full Text] [Related]
26. Intracranial hemorrhage pattern in the patients with factor XIII deficiency. Naderi M; Zarei T; Haghpanah S; Eshghi P; Miri-Moghaddam E; Karimi M Ann Hematol; 2014 Apr; 93(4):693-7. PubMed ID: 24149912 [TBL] [Abstract][Full Text] [Related]
27. Application of HUMF13A01 (AAAG)n STR polymorphism to the genetic diagnosis of coagulation factor XIII deficiency. Kangsadalampai S; Coggan M; Caglayan SH; Aktuglu G; Board PG Thromb Haemost; 1996 Dec; 76(6):879-82. PubMed ID: 8972004 [TBL] [Abstract][Full Text] [Related]
28. [Clinical aspects of factor XIII defect]. Ikkala E Thromb Diath Haemorrh Suppl; 1968; 28():13-21; discussion 23-54. PubMed ID: 4951265 [No Abstract] [Full Text] [Related]
30. Congenital factor XIII deficiency. Shukla J; Dube B; Dube RK; Das BK; Mishra OP J Assoc Physicians India; 1993 Nov; 41(11):731. PubMed ID: 8005932 [No Abstract] [Full Text] [Related]
31. The human fibrin-stabilizing factors. Bohn H Mol Cell Biochem; 1978 Jun; 20(2):67-75. PubMed ID: 353534 [No Abstract] [Full Text] [Related]
32. [An infant with umbilical cord and intracranial hemorrhage--severe factor XIII deficiency]. von der Weid N; Furlan M; Siegenthaler I; Lämmle B Ther Umsch; 1999 Sep; 56(9):544-6. PubMed ID: 10517131 [TBL] [Abstract][Full Text] [Related]
33. Factor XIII deficiency: pathogenic mechanisms and clinical significance. Egbring R; Kröniger A; Seitz R Semin Thromb Hemost; 1996; 22(5):419-25. PubMed ID: 8989826 [TBL] [Abstract][Full Text] [Related]
34. Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms. Biswas A; Ivaskevicius V; Thomas A; Oldenburg J Hamostaseologie; 2014; 34(2):160-6. PubMed ID: 24503678 [TBL] [Abstract][Full Text] [Related]
35. Factor XIII deficiency: report of a case complicated by splenic rupture. Bregman R; Davis RB; Schreiner GC; Pratt PT Nebr Med J; 1976 Mar; 61(3):80-3. PubMed ID: 1272449 [No Abstract] [Full Text] [Related]
36. Diagnosis and management of severe congenital factor XIII deficiency in the Emergency Department: lessons from a "model" family. Bertamino M; Banov L; Molinari AC Blood Transfus; 2015 Apr; 13(2):324-7. PubMed ID: 25369590 [No Abstract] [Full Text] [Related]
37. Clinical and laboratory features of congenital factor XIII deficiency. Al-Sharif FZ; Aljurf MD; Al-Momen AM; Ajlan AM; Musa MO; Al-Nounou RM; Al-Mohareb FI; Alomar HM; Zaidi ZZ; Al-Zahrani HA Saudi Med J; 2002 May; 23(5):552-4. PubMed ID: 12070580 [TBL] [Abstract][Full Text] [Related]
38. [Substitution of F XIII concentrate in ulcerative colitis]. Lorenz R; Clemens R; Karl M; Classen M Z Gastroenterol; 1989 Feb; 27(2):87-90. PubMed ID: 2658393 [TBL] [Abstract][Full Text] [Related]
39. The fibrin-stabilizing factor. A decade of progress. Mandel EE Ann Clin Lab Sci (1971); 1971; 1(1):92-9. PubMed ID: 4949766 [No Abstract] [Full Text] [Related]
40. Quality of life of people with hereditary factor XIII deficiency treated at a reference centre. Drumond A; Camelo RM Haemophilia; 2021 Sep; 27(5):e649-e653. PubMed ID: 34329524 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]