EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.3.2.13 | Abortion, Habitual |
10638168 |
[Congenital factor XIII deficiency in pregnancy. A case report] |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
3
1
0 |
| 2.3.2.13 | Abortion, Habitual |
10674253 |
Bleeding risk and reproductive capacity among patients with factor XIII deficiency: a case presentation and review of the literature. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
3
2
1 |
| 2.3.2.13 | Abortion, Habitual |
11057855 |
Factor XIII deficiency causing mutation, Ser295Arg, in exon 7 of the factor XIIIA gene. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
2
1
0 |
| 2.3.2.13 | Abortion, Habitual |
11334902 |
Factor XII but not protein C, protein S, antithrombin III, or factor XIII is a predictor of recurrent miscarriage. |
diagnostic usage
therapeutic application
unassigned |
2
1
0 |
| 2.3.2.13 | Abortion, Habitual |
16052406 |
Genetic factors in fetal growth restriction and miscarriage. |
causal interaction
diagnostic usage
unassigned |
3
1
0 |
| 2.3.2.13 | Abortion, Habitual |
16844105 |
Prevalence of the coagulation factor XIII polymorphism Val34Leu in women with recurrent miscarriage. |
causal interaction
diagnostic usage
unassigned |
2
2
0 |
| 2.3.2.13 | Abortion, Habitual |
17371605 |
Congenital blood coagulation factor XIII deficiency and successful deliveries: a review of the literature. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
2
1
0 |
| 2.3.2.13 | Abortion, Habitual |
17470597 |
Fibrinolytic defects and recurrent miscarriage: a systematic review and meta-analysis. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
3
2
1
0 |
| 2.3.2.13 | Abortion, Habitual |
21852211 |
Management of pregnancy and delivery in women with inherited bleeding disorders. |
causal interaction
therapeutic application
unassigned |
3
2
0 |
| 2.3.2.13 | Abortion, Habitual |
24702949 |
Prevalence of coagulation factor XIII and plasminogen activator inhibitor-1 gene polymorphisms among Egyptian women suffering from unexplained primary recurrent miscarriage. |
diagnostic usage
ongoing research
unassigned |
1
1
0 |
