-
1
-
-
0023546828
-
Laboratory screening of inherited thrombotic syndromes
-
1:STN:280:BieD3MfmsVQ%3D
-
Mannucci PM, Tripoli A (1987) Laboratory screening of inherited thrombotic syndromes. Thromb Haemost 57:247-251 1:STN:280:BieD3MfmsVQ%3D
-
(1987)
Thromb. Haemost.
, vol.57
, pp. 247-251
-
-
Mannucci, P.M.1
Tripoli, A.2
-
2
-
-
0032776505
-
Congenital thrombophilia and thrombosis: A study in a single centre
-
1:STN:280:DyaK1MvitFGgsg%3D%3D
-
Lawson SE, Butler D, Enayat MS, Williams MD (1999) Congenital thrombophilia and thrombosis: A study in a single centre. Arch Dis Child 81:176-178 1:STN:280:DyaK1MvitFGgsg%3D%3D
-
(1999)
Arch. Dis. Child
, vol.81
, pp. 176-178
-
-
Lawson, S.E.1
Butler, D.2
Enayat, M.S.3
Williams, M.D.4
-
3
-
-
0029086663
-
Development hemostasis. Relevance to thromboembolic complications in pediatric patients
-
1:CAS:528:DyaK2MXnvVSqsLo%3D
-
Andrew M (1995) Development hemostasis. Relevance to thromboembolic complications in pediatric patients. Thromb Haemost 74:415-425 1:CAS:528:DyaK2MXnvVSqsLo%3D
-
(1995)
Thromb. Haemost.
, vol.74
, pp. 415-425
-
-
Andrew, M.1
-
4
-
-
0030857264
-
Neonatal symptomatic thromboembolism in Germany: Two year survey
-
Gottl UN, Von Kries R, Gobel U (1997) Neonatal symptomatic thromboembolism in Germany: Two year survey. Arch Dis Child 76:F163-F167
-
(1997)
Arch. Dis. Child
, vol.76
-
-
Gottl, U.N.1
Von Kries, R.2
Gobel, U.3
-
5
-
-
0030746618
-
Thrombophilia is a multigenic disorder
-
1:CAS:528:DyaK2sXktFelsb4%3D
-
Seligsohn U, Zivelin A (1997) Thrombophilia is a multigenic disorder. Thromb Haemost 78:297-301
-
(1997)
Thromb. Haemost.
, vol.78
, pp. 297-301
-
-
Seligsohn, U.1
Zivelin, A.2
-
6
-
-
0029876985
-
Inherited thrombophilia: Pathogenesis, clinical syndromes, and management
-
8611675
-
De Stefano V, Finazzi G, Mannucci PM (1996) Inherited thrombophilia: pathogenesis, clinical syndromes, and management. Blood 87:3531-3544 8611675
-
(1996)
Blood
, vol.87
, pp. 3531-3544
-
-
De Stefano, V.1
Finazzi, G.2
Mannucci, P.M.3
-
7
-
-
0033800605
-
Symptomatic ischemic stroke in full term neonate: Role of acquired and genetic prothrombotic risk factors
-
1:CAS:528:DC%2BD3cXnsVKqtrY%3D
-
Gunther G, Junker R, Strater R, Sehobers R, Kurnik K, Heller C et al (2000) Symptomatic ischemic stroke in full term neonate: Role of acquired and genetic prothrombotic risk factors. Stroke 31:2437-2441 1:CAS:528:DC%2BD3cXnsVKqtrY%3D
-
(2000)
Stroke
, vol.31
, pp. 2437-2441
-
-
Gunther, G.1
Junker, R.2
Strater, R.3
Sehobers, R.4
Kurnik, K.5
Heller, C.6
-
8
-
-
0342507197
-
Increased lipoprotein (a) is an important risk factor for venous thromboembolism in childhood
-
10449697
-
Gottl UN, Junker R, Hartmeier M, Kock HG, Munchow N, Assmann G et al (1999) Increased lipoprotein (a) is an important risk factor for venous thromboembolism in childhood. Circulation 100:743-748 10449697
-
(1999)
Circulation
, vol.100
, pp. 743-748
-
-
Gottl, U.N.1
Junker, R.2
Hartmeier, M.3
Kock, H.G.4
Munchow, N.5
Assmann, G.6
-
9
-
-
0033387167
-
Factor V G 1691 A and prothrombin G 20210 A in childhood spontaneous venous thrombosis - Evidence of an age-dependent thrombotic onset in carriers of factor V G 1691 A and prothrombin G 20210 A mutation
-
1:CAS:528:DC%2BD3cXpt1yqsQ%3D%3D
-
Schobers R, Junker R, Auberger K, Munchow N, Burdach S, Nowak Gottl UN (1999) Factor V G 1691 A and prothrombin G 20210 A in childhood spontaneous venous thrombosis - Evidence of an age-dependent thrombotic onset in carriers of factor V G 1691 A and prothrombin G 20210 A mutation. Eur J Pediatr 158:S105-S108 1:CAS:528:DC%2BD3cXpt1yqsQ%3D%3D
-
(1999)
Eur. J. Pediatr.
, vol.158
-
-
Schobers, R.1
Junker, R.2
Auberger, K.3
Munchow, N.4
Burdach, S.5
Nowak Gottl, U.N.6
-
10
-
-
10544223737
-
Prevalence of factor V Leiden in children with thromboembolism
-
10.1007/s004310050523
-
Aschka I, Auman V, Bergmann F, Budde U, Eberl W, Eckhof-Donovan S et al (1996) Prevalence of factor V Leiden in children with thromboembolism. Eur J Pediatr 155:1009-1014 10.1007/s004310050523
-
(1996)
Eur. J. Pediatr.
, vol.155
, pp. 1009-1014
-
-
Aschka, I.1
Auman, V.2
Bergmann, F.3
Budde, U.4
Eberl, W.5
Eckhof-Donovan, S.6
-
11
-
-
0034919297
-
Thromboembolism in newborns, infants and children
-
11487037
-
Gottl UN, Kosch A, Schlegel N (2001) Thromboembolism in newborns, infants and children. Thromb Haemost 86:464-474 11487037
-
(2001)
Thromb. Haemost.
, vol.86
, pp. 464-474
-
-
Gottl, U.N.1
Kosch, A.2
Schlegel, N.3
-
12
-
-
0032833721
-
Prothrombin G 20210 A gene mutation and further prothrombotic risk factors in childhood thrombophilia
-
1:CAS:528:DyaK1MXmvFGitbo%3D
-
Junker R, Koch HG, Auberger K, Munchow N, Ehrenforth S, Gottl UN (1999) Prothrombin G 20210 A gene mutation and further prothrombotic risk factors in childhood thrombophilia. Arterioscler Thromb Vasc Biol 19:2568-2572 1:CAS:528:DyaK1MXmvFGitbo%3D
-
(1999)
Arterioscler. Thromb. Vasc. Biol.
, vol.19
, pp. 2568-2572
-
-
Junker, R.1
Koch, H.G.2
Auberger, K.3
Munchow, N.4
Ehrenforth, S.5
Gottl, U.N.6
-
13
-
-
0029850530
-
A common genetic variation in the 3′ untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
1:CAS:528:DyaK28XntVahsLg%3D
-
Poort SR, Rosendaal FR, Reitsma PH, Bertina RM (1996) A common genetic variation in the 3′ untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 88:3698-3703 1:CAS:528:DyaK28XntVahsLg%3D
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
15
-
-
0034919297
-
Thromboembolism in newborns, infants and children
-
11487037
-
Gottl UN, Kosch A, Schlegel N (2001) Thromboembolism in newborns, infants and children. Thromb Haemost 86:464-474 11487037
-
(2001)
Thromb. Haemost.
, vol.86
, pp. 464-474
-
-
Gottl, U.N.1
Kosch, A.2
Schlegel, N.3
-
16
-
-
0033373297
-
Prothrombotic risk factors in childhood stroke and venous thrombosis
-
10650849
-
Heller C, Becker S, Scharrer, Kreuz W (1999) Prothrombotic risk factors in childhood stroke and venous thrombosis. Eur J Pediatr 158 [Suppl 3]:S117-S121 10650849
-
(1999)
Eur. J. Pediatr.
, vol.158
, Issue.SUPPL. 3
-
-
Heller, C.1
Becker, S.2
Scharrer, K.W.3
-
17
-
-
0030943180
-
Pediatric thrombo-embolism: The influence of non-genetic factors and the role of activated protein C resistance and protein C deficiency
-
10.1007/s004310050600
-
Ultenreuther MM, Fischer B, Vetter C, Hellmann U, Otting S, Zicmer G et al (1997) Pediatric thrombo-embolism: The influence of non-genetic factors and the role of activated protein C resistance and protein C deficiency. Eur J Pediatr 156:277-281 10.1007/s004310050600
-
(1997)
Eur. J. Pediatr.
, vol.156
, pp. 277-281
-
-
Ultenreuther, M.M.1
Fischer, B.2
Vetter, C.3
Hellmann, U.4
Otting, S.5
Zicmer, G.6
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