-
1
-
-
0036210038
-
Clinical outcomes and resource utilization associated with haemophilia care in Europe
-
Schramm W, Royal S, Kroner B, et al. Clinical outcomes and resource utilization associated with haemophilia care in Europe. Haemophilia 2002;8:33-43
-
(2002)
Haemophilia
, vol.8
, pp. 33-43
-
-
Schramm, W.1
Royal, S.2
Kroner, B.3
-
2
-
-
0034003628
-
Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France. The French Study Group, secretariat. haemophiles@cch.ap-hop-paris.fr
-
Molho P, Rolland N, Lebrun T, et al. Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France. The French Study Group, secretariat. haemophiles@cch.ap-hop-paris.fr. Haemophilia 2000;6:23-32
-
(2000)
Haemophilia
, vol.6
, pp. 23-32
-
-
Molho, P.1
Rolland, N.2
Lebrun, T.3
-
3
-
-
0028004222
-
A longitudinal study of orthopaedic outcomes for severe factor-VIII-deficient haemophiliacs. The Orthopaedic Outcome Study Group
-
Aledort LM, Haschmeyer RH, Pettersson H. A longitudinal study of orthopaedic outcomes for severe factor-VIII-deficient haemophiliacs. The Orthopaedic Outcome Study Group. J Intern Med 1994;236:391-399
-
(1994)
J Intern Med
, vol.236
, pp. 391-399
-
-
Aledort, L.M.1
Haschmeyer, R.H.2
Pettersson, H.3
-
5
-
-
0035525732
-
Discrepancies between genotype and phenotype in hematology: An important frontier
-
Beutler E. Discrepancies between genotype and phenotype in hematology: an important frontier. Blood 2001;98:2597-2602
-
(2001)
Blood
, vol.98
, pp. 2597-2602
-
-
Beutler, E.1
-
6
-
-
22544473061
-
The Malmo International Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A
-
Astermark J, Oldenburg J, Escobar M, White GC II, Berntorp E. The Malmo International Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A. Haematologica 2005; 90:924-931
-
(2005)
Haematologica
, vol.90
, pp. 924-931
-
-
Astermark, J.1
Oldenburg, J.2
Escobar, M.3
White II, G.C.4
Berntorp, E.5
-
7
-
-
0028029477
-
Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation
-
Vandenbroucke JP, Koster T, Briet E, Reitsma PH, Bertina RM, Rosendaal FR. Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation. Lancet 1994;344:1453-1457
-
(1994)
Lancet
, vol.344
, pp. 1453-1457
-
-
Vandenbroucke, J.P.1
Koster, T.2
Briet, E.3
Reitsma, P.H.4
Bertina, R.M.5
Rosendaal, F.R.6
-
8
-
-
4444334037
-
Do prothrombotic factors influence clinical phenotype of severe haemophilia? A review of the literature
-
van Dijk K, van der Bom JG, Fischer K, Grobbee DE, van den Berg HM. Do prothrombotic factors influence clinical phenotype of severe haemophilia? A review of the literature. Thromb Haemost 2004;92:305-310
-
(2004)
Thromb Haemost
, vol.92
, pp. 305-310
-
-
van Dijk, K.1
van der Bom, J.G.2
Fischer, K.3
Grobbee, D.E.4
van den Berg, H.M.5
-
9
-
-
17844380517
-
Factor VIII half-life and clinical phenotype of severe hemophilia A
-
van Dijk K, van der Bom JG, Lenting PJ, et al. Factor VIII half-life and clinical phenotype of severe hemophilia A. Haematologica 2005;90:494-498
-
(2005)
Haematologica
, vol.90
, pp. 494-498
-
-
van Dijk, K.1
van der Bom, J.G.2
Lenting, P.J.3
-
10
-
-
0018741903
-
The knee joint in hemophilia
-
Handelsman JE. The knee joint in hemophilia. Orthop Clin North Am 1979;10:139-173
-
(1979)
Orthop Clin North Am
, vol.10
, pp. 139-173
-
-
Handelsman, J.E.1
-
11
-
-
0018152310
-
Management of musculoskeletal problems in the hemophilias
-
Hoskinson J, Duthie RB. Management of musculoskeletal problems in the hemophilias. Orthop Clin North Am 1978;9:455-480
-
(1978)
Orthop Clin North Am
, vol.9
, pp. 455-480
-
-
Hoskinson, J.1
Duthie, R.B.2
-
12
-
-
0019465425
-
The pathogenesis of chronic haemophilic arthropathy
-
Stein H, Duthie RB. The pathogenesis of chronic haemophilic arthropathy. J Bone Joint Surg Br 1981;63B: 601-609
-
(1981)
J Bone Joint Surg Br
, vol.63 B
, pp. 601-609
-
-
Stein, H.1
Duthie, R.B.2
-
13
-
-
2642578428
-
Initiation of degenerative joint damage by experimental bleeding combined with loading of the joint: A possible mechanism of hemophilic arthropathy
-
Hooiveld MJ, Roosendaal G, Jacobs KM, et al. Initiation of degenerative joint damage by experimental bleeding combined with loading of the joint: a possible mechanism of hemophilic arthropathy. Arthritis Rheum 2004;50:2024-2031
-
(2004)
Arthritis Rheum
, vol.50
, pp. 2024-2031
-
-
Hooiveld, M.J.1
Roosendaal, G.2
Jacobs, K.M.3
-
14
-
-
0017601179
-
Hemophilic arthropathy. Current concepts of pathogenesis and management
-
Arnold WD, Hilgartner MW. Hemophilic arthropathy. Current concepts of pathogenesis and management. J Bone Joint Surg Am 1977;59:287-305
-
(1977)
J Bone Joint Surg Am
, vol.59
, pp. 287-305
-
-
Arnold, W.D.1
Hilgartner, M.W.2
-
16
-
-
0036529818
-
The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia
-
Fischer K, van der Bom JG, Mauser-Bunschoten EP, et al. The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia. Blood 2002; 99:2337-2341
-
(2002)
Blood
, vol.99
, pp. 2337-2341
-
-
Fischer, K.1
van der Bom, J.G.2
Mauser-Bunschoten, E.P.3
-
17
-
-
0343820051
-
When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10-year single-centre PUP study
-
Pollmann H, Richter H, Ringkamp H, Jurgens H. When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10-year single-centre PUP study. Eur J Pediatr 1999;158(Suppl 3):S166-S170
-
(1999)
Eur J Pediatr
, vol.158
, Issue.SUPPL. 3
-
-
Pollmann, H.1
Richter, H.2
Ringkamp, H.3
Jurgens, H.4
-
18
-
-
0006699504
-
-
Ramgren O. Haemophilia in Sweden. III. Symptomatology, with special reference to differences between haemophilia A and B. Acta Med Scand 1962;171:237-242
-
Ramgren O. Haemophilia in Sweden. III. Symptomatology, with special reference to differences between haemophilia A and B. Acta Med Scand 1962;171:237-242
-
-
-
-
19
-
-
0015619281
-
A three-year study of adolescent boys suffering from haemophilia and allied disorders
-
Rainsford SG, Hall A. A three-year study of adolescent boys suffering from haemophilia and allied disorders. Br J Haematol 1973;24:539-551
-
(1973)
Br J Haematol
, vol.24
, pp. 539-551
-
-
Rainsford, S.G.1
Hall, A.2
-
20
-
-
24644521462
-
Variability in clinical phenotype of severe haemophilia: The role of the first joint bleed
-
van Dijk K, Fischer K, van der Bom JG, Grobbee DE, van den Berg HM. Variability in clinical phenotype of severe haemophilia: the role of the first joint bleed. Haemophilia 2005;11:438-443
-
(2005)
Haemophilia
, vol.11
, pp. 438-443
-
-
van Dijk, K.1
Fischer, K.2
van der Bom, J.G.3
Grobbee, D.E.4
van den Berg, H.M.5
-
21
-
-
11144326206
-
A survey of factor prophylaxis in the Canadian haemophilia A population
-
Blanchette P, Rivard G, Israels S, et al. A survey of factor prophylaxis in the Canadian haemophilia A population. Haemophilia 2004;10:679-683
-
(2004)
Haemophilia
, vol.10
, pp. 679-683
-
-
Blanchette, P.1
Rivard, G.2
Israels, S.3
-
22
-
-
0036860471
-
Paradoxical hyperfibrinolysis is associated with a more intensely haemorrhagic phenotype in severe congenital haemophilia
-
Grunewald M, Siegemund A, Grunewald A, Konegan A, Koksch M, Griesshammer M. Paradoxical hyperfibrinolysis is associated with a more intensely haemorrhagic phenotype in severe congenital haemophilia. Haemophilia 2002;8:768-775
-
(2002)
Haemophilia
, vol.8
, pp. 768-775
-
-
Grunewald, M.1
Siegemund, A.2
Grunewald, A.3
Konegan, A.4
Koksch, M.5
Griesshammer, M.6
-
23
-
-
0028855944
-
Low prevalence of the factor V Leiden mutation among "severe" hemophiliacs with a "milder" bleeding diathesis
-
Arbini AA, Mannucci PM, Bauer KA. Low prevalence of the factor V Leiden mutation among "severe" hemophiliacs with a "milder" bleeding diathesis. Thromb Haemost 1995; 74:1255-1258
-
(1995)
Thromb Haemost
, vol.74
, pp. 1255-1258
-
-
Arbini, A.A.1
Mannucci, P.M.2
Bauer, K.A.3
-
25
-
-
34447314172
-
Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients
-
Shetty S, Vora S, Kulkarni B, et al. Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients. Br J Haematol 2007;138:541-544
-
(2007)
Br J Haematol
, vol.138
, pp. 541-544
-
-
Shetty, S.1
Vora, S.2
Kulkarni, B.3
-
26
-
-
4944256880
-
Dose and response in haemophilia-optimization of factor replacement therapy
-
Srivastava A. Dose and response in haemophilia-optimization of factor replacement therapy. Br J Haematol 2004;127:12-25
-
(2004)
Br J Haematol
, vol.127
, pp. 12-25
-
-
Srivastava, A.1
-
27
-
-
0027214492
-
Prophylaxis: Musculoskeletal evaluation
-
Gilbert MS. Prophylaxis: musculoskeletal evaluation. Semin Hematol 1993;30:3-6
-
(1993)
Semin Hematol
, vol.30
, pp. 3-6
-
-
Gilbert, M.S.1
-
29
-
-
31444453676
-
Functional assessment of arthropathy-an international perspective
-
Poonnoose PM, Srivastava A. Functional assessment of arthropathy-an international perspective. Semin Hematol 2006;43:S27-S32
-
(2006)
Semin Hematol
, vol.43
-
-
Poonnoose, P.M.1
Srivastava, A.2
-
30
-
-
4043144279
-
Haemophilia and thrombophilia: An unexpected association!
-
Dargaud Y, Meunier S, Negrier C. Haemophilia and thrombophilia: an unexpected association! Haemophilia 2004;10:319-326
-
(2004)
Haemophilia
, vol.10
, pp. 319-326
-
-
Dargaud, Y.1
Meunier, S.2
Negrier, C.3
-
31
-
-
0036125865
-
The utility of activated partial thromboplastin time (aPTT) clot waveform analysis in the investigation of hemophilia A patients with very low levels of factor VIII activity (FVIII:C)
-
Shima M, Matsumoto T, Fukuda K, et al. The utility of activated partial thromboplastin time (aPTT) clot waveform analysis in the investigation of hemophilia A patients with very low levels of factor VIII activity (FVIII:C). Thromb Haemost 2002;87:436-441
-
(2002)
Thromb Haemost
, vol.87
, pp. 436-441
-
-
Shima, M.1
Matsumoto, T.2
Fukuda, K.3
-
32
-
-
0035129399
-
Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors
-
Escuriola Ettingshausen C, Halimeh S, Kurnik K, et al. Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors. Thromb Haemost 2001;85:218-220
-
(2001)
Thromb Haemost
, vol.85
, pp. 218-220
-
-
Escuriola Ettingshausen, C.1
Halimeh, S.2
Kurnik, K.3
-
33
-
-
0035134231
-
Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one-stage assay
-
Ghosh K, Shetty S, Mohanty D. Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one-stage assay. Haemophilia 2001;7:9-12
-
(2001)
Haemophilia
, vol.7
, pp. 9-12
-
-
Ghosh, K.1
Shetty, S.2
Mohanty, D.3
-
34
-
-
4444376084
-
Whole blood clot formation phenotypes in hemophilia A and rare coagulation disorders. Patterns of response to recombinant factor VIIa
-
Sorensen B, Ingerslev J. Whole blood clot formation phenotypes in hemophilia A and rare coagulation disorders. Patterns of response to recombinant factor VIIa. J Thromb Haemost 2004;2:102-110
-
(2004)
J Thromb Haemost
, vol.2
, pp. 102-110
-
-
Sorensen, B.1
Ingerslev, J.2
-
35
-
-
15344343052
-
Evaluation of thrombin generating capacity in plasma from patients with haemophilia A and B
-
Dargaud Y, Beguin S, Lienhart A, et al. Evaluation of thrombin generating capacity in plasma from patients with haemophilia A and B. Thromb Haemost 2005;93:475-480
-
(2005)
Thromb Haemost
, vol.93
, pp. 475-480
-
-
Dargaud, Y.1
Beguin, S.2
Lienhart, A.3
-
36
-
-
0242575183
-
Thrombin generation in severe haemophilia A and B: The endogenous thrombin potential in platelet-rich plasma
-
Siegemund T, Petras S, Siegemund A, Scholz U, Engelmann L. Thrombin generation in severe haemophilia A and B: the endogenous thrombin potential in platelet-rich plasma. Thromb Haemost 2003;90:781-786
-
(2003)
Thromb Haemost
, vol.90
, pp. 781-786
-
-
Siegemund, T.1
Petras, S.2
Siegemund, A.3
Scholz, U.4
Engelmann, L.5
-
37
-
-
33645582371
-
The measurement of low levels of factor VIII or factor K in hemophilia A and hemophilia B plasma by clot waveform analysis and thrombin generation assay
-
Matsumoto T, Shima M, Takeyama M, et al. The measurement of low levels of factor VIII or factor K in hemophilia A and hemophilia B plasma by clot waveform analysis and thrombin generation assay. J Thromb Haemost 2006;4:377-384
-
(2006)
J Thromb Haemost
, vol.4
, pp. 377-384
-
-
Matsumoto, T.1
Shima, M.2
Takeyama, M.3
-
39
-
-
0034016852
-
Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A
-
Lee DH, Walker IR, Teitel J, et al. Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A. Thromb Haemost 2000;83:387-391
-
(2000)
Thromb Haemost
, vol.83
, pp. 387-391
-
-
Lee, D.H.1
Walker, I.R.2
Teitel, J.3
-
40
-
-
0037313997
-
Haemophilia and thrombophilia. What do we learn about combined inheritance of both genetic variations?
-
Nowak-Götd U, Escuriola C, Kurnik K, et al. Haemophilia and thrombophilia. What do we learn about combined inheritance of both genetic variations? Hamostaseologie 2003;23:36-40
-
(2003)
Hamostaseologie
, vol.23
, pp. 36-40
-
-
Nowak-Götd, U.1
Escuriola, C.2
Kurnik, K.3
-
41
-
-
43149103132
-
-
Jayandharan GR, Nair SC, Poonoose P, et al. Polymorphisms in coagulant and inflammatory genes modify the phenotype of severe hemophilia A and B. J Thomb Haemost 2007;5(Suppl 1):P_W_681
-
Jayandharan GR, Nair SC, Poonoose P, et al. Polymorphisms in coagulant and inflammatory genes modify the phenotype of severe hemophilia A and B. J Thomb Haemost 2007;5(Suppl 1):P_W_681
-
-
-
-
42
-
-
34247876186
-
Phenotype of severe hemophilia A and plasma levels of risk factors for thrombosis
-
van Dijk K, van der Bom JG, Fischer K, de Groot PG, van den Berg HM. Phenotype of severe hemophilia A and plasma levels of risk factors for thrombosis. J Thromb Haemost 2007;5:1062-1064
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1062-1064
-
-
van Dijk, K.1
van der Bom, J.G.2
Fischer, K.3
de Groot, P.G.4
van den Berg, H.M.5
-
43
-
-
0034757342
-
The defective down regulation of fibrinolysis in haemophilia A can be restored by increasing the TAFI plasma concentration
-
Mosnier LO, Lisman T, van den Berg HM, Nieuwenhuis HK, Meijers JC, Bouma BN. The defective down regulation of fibrinolysis in haemophilia A can be restored by increasing the TAFI plasma concentration. Thromb Haemost 2001;86:1035-1039
-
(2001)
Thromb Haemost
, vol.86
, pp. 1035-1039
-
-
Mosnier, L.O.1
Lisman, T.2
van den Berg, H.M.3
Nieuwenhuis, H.K.4
Meijers, J.C.5
Bouma, B.N.6
-
44
-
-
24644437294
-
Identification of factor VIII gene mutations in 101 patients with haemophilia A: Mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions
-
Jayandharan G, Shaji RV, Baidya S, Nair SC, Chandy M, Srivastava A. Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions. Haemophilia 2005;11:481-491
-
(2005)
Haemophilia
, vol.11
, pp. 481-491
-
-
Jayandharan, G.1
Shaji, R.V.2
Baidya, S.3
Nair, S.C.4
Chandy, M.5
Srivastava, A.6
-
45
-
-
27144448063
-
Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India
-
Jayandharan GR, Shaji RV, Baidya S, Nair SC, Chandy M, Srivastava A. Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India. Thromb Haemost 2005;94:883-886
-
(2005)
Thromb Haemost
, vol.94
, pp. 883-886
-
-
Jayandharan, G.R.1
Shaji, R.V.2
Baidya, S.3
Nair, S.C.4
Chandy, M.5
Srivastava, A.6
-
46
-
-
0037330233
-
The molecular basis of hemophilia A: Genotype-phenotype relationships and inhibitor development
-
Goodeve AC, Peake IR. The molecular basis of hemophilia A: genotype-phenotype relationships and inhibitor development. Semin Thromb Hemost 2003;29:23-30
-
(2003)
Semin Thromb Hemost
, vol.29
, pp. 23-30
-
-
Goodeve, A.C.1
Peake, I.R.2
-
47
-
-
14044254724
-
Elevated clotting factor levels and venous thrombosis
-
Bertina RM. Elevated clotting factor levels and venous thrombosis. Pathophysiol Haemost Thromb 2003/2004;33: 395-400
-
(2003)
Pathophysiol Haemost Thromb
, vol.33
, pp. 395-400
-
-
Bertina, R.M.1
-
48
-
-
0037375566
-
Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis
-
Endler G, Mannhalter C. Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis. Clin Chim Acta 2003;330:31-55
-
(2003)
Clin Chim Acta
, vol.330
, pp. 31-55
-
-
Endler, G.1
Mannhalter, C.2
-
49
-
-
0032495540
-
Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction
-
Iacoviello L, Di Castelnuovo A, De Knijff P, et al. Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction. N Engl J Med 1998;338: 79-85
-
(1998)
N Engl J Med
, vol.338
, pp. 79-85
-
-
Iacoviello, L.1
Di Castelnuovo, A.2
De Knijff, P.3
-
50
-
-
23644433169
-
Quantification of thrombin activatable fibrinolysis inhibitor (TAFI) gene polymorphism effects on plasma levels of TAFI measured with assays insensitive to isoform-dependent artefact
-
Frere C, Morange PE, Saut N, et al. Quantification of thrombin activatable fibrinolysis inhibitor (TAFI) gene polymorphism effects on plasma levels of TAFI measured with assays insensitive to isoform-dependent artefact. Thromb Haemost 2005;94:373-379
-
(2005)
Thromb Haemost
, vol.94
, pp. 373-379
-
-
Frere, C.1
Morange, P.E.2
Saut, N.3
-
51
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995;10: 111-113
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
52
-
-
0037308310
-
Blood-induced joint damage: Longterm effects in vitro and in vivo
-
Hooiveld M, Roosendaal G, Vianen M, van den Berg M, Bijlsma J, Lafeber F. Blood-induced joint damage: longterm effects in vitro and in vivo. J Rheumatol 2003;30:339-344
-
(2003)
J Rheumatol
, vol.30
, pp. 339-344
-
-
Hooiveld, M.1
Roosendaal, G.2
Vianen, M.3
van den Berg, M.4
Bijlsma, J.5
Lafeber, F.6
-
53
-
-
0031774695
-
Iron deposits and catabolic properties of synovial tissue from patients with haemophilia
-
Roosendaal G, Vianen ME, Wenting MJ, et al. Iron deposits and catabolic properties of synovial tissue from patients with haemophilia. J Bone Joint Surg Br 1998;80: 540-545
-
(1998)
J Bone Joint Surg Br
, vol.80
, pp. 540-545
-
-
Roosendaal, G.1
Vianen, M.E.2
Wenting, M.J.3
-
54
-
-
4644248645
-
Pathobiology of hemophilic synovitis I: Overexpression of mdm2 oncogene
-
Hakobyan N, Kazarian T, Jabbar AA, Jabbar KJ, Valentino LA. Pathobiology of hemophilic synovitis I: overexpression of mdm2 oncogene. Blood 2004;104:2060-2064
-
(2004)
Blood
, vol.104
, pp. 2060-2064
-
-
Hakobyan, N.1
Kazarian, T.2
Jabbar, A.A.3
Jabbar, K.J.4
Valentino, L.A.5
-
55
-
-
0028043648
-
Stimulation of human synovial cell DNA synthesis by iron
-
Nishiya K. Stimulation of human synovial cell DNA synthesis by iron. J Rheumatol 1994;21:1802-1807
-
(1994)
J Rheumatol
, vol.21
, pp. 1802-1807
-
-
Nishiya, K.1
-
56
-
-
0022641206
-
Relationship between iron deposits and tissue damage in the synovium: An ultrastructural study
-
Morris CJ, Blake DR, Wainwright AC, Steven MM. Relationship between iron deposits and tissue damage in the synovium: an ultrastructural study. Ann Rheum Dis 1986; 45:21-26
-
(1986)
Ann Rheum Dis
, vol.45
, pp. 21-26
-
-
Morris, C.J.1
Blake, D.R.2
Wainwright, A.C.3
Steven, M.M.4
-
57
-
-
0036682499
-
c-myc proto-oncogene expression in hemophilic synovitis: In vitro studies of the effects of iron and ceramide
-
Wen FQ, Jabbar AA, Chen YX, Kazarian T, Patel DA, Valentino LA. c-myc proto-oncogene expression in hemophilic synovitis: in vitro studies of the effects of iron and ceramide. Blood 2002;100:912-916
-
(2002)
Blood
, vol.100
, pp. 912-916
-
-
Wen, F.Q.1
Jabbar, A.A.2
Chen, Y.X.3
Kazarian, T.4
Patel, D.A.5
Valentino, L.A.6
-
58
-
-
33746488770
-
Clinical significance of IL-18, IL-15, IL-12 and TNF-alpha measurement in rheumatoid arthritis
-
Petrovic-Rackov L, Pejnovic N. Clinical significance of IL-18, IL-15, IL-12 and TNF-alpha measurement in rheumatoid arthritis. Clin Rheumatol 2006;25:448-452
-
(2006)
Clin Rheumatol
, vol.25
, pp. 448-452
-
-
Petrovic-Rackov, L.1
Pejnovic, N.2
-
59
-
-
31444456793
-
Could single-nucleotide polymorphisms (SNPs) affecting the tumour necrosis factor promoter be considered as part of rheumatoid arthritis evolution?
-
Aguillon JC, Cruzat A, Aravena O, Salazar L, Llanos C, Cuchacovich M. Could single-nucleotide polymorphisms (SNPs) affecting the tumour necrosis factor promoter be considered as part of rheumatoid arthritis evolution? Immunobiology 2006;211:75-84
-
(2006)
Immunobiology
, vol.211
, pp. 75-84
-
-
Aguillon, J.C.1
Cruzat, A.2
Aravena, O.3
Salazar, L.4
Llanos, C.5
Cuchacovich, M.6
-
60
-
-
0034536265
-
Tumour necrosis factor-alpha gene polymorphism: Implications in kidney transplantation
-
Poli F, Boschiero L, Giannoni F, et al. Tumour necrosis factor-alpha gene polymorphism: implications in kidney transplantation. Cytokine 2000;12:1778-1783
-
(2000)
Cytokine
, vol.12
, pp. 1778-1783
-
-
Poli, F.1
Boschiero, L.2
Giannoni, F.3
-
61
-
-
0031033902
-
Polymorphism at the TNF loci in rheumatoid arthritis
-
Vinasco J, Beraun Y, Nieto A, et al. Polymorphism at the TNF loci in rheumatoid arthritis. Tissue Antigens 1997;49: 74-78
-
(1997)
Tissue Antigens
, vol.49
, pp. 74-78
-
-
Vinasco, J.1
Beraun, Y.2
Nieto, A.3
-
62
-
-
0033693715
-
Are differences in interleukin 10 production associated with joint damage?
-
Huizinga TW, Keijsers V, Yanni G, et al. Are differences in interleukin 10 production associated with joint damage? Rheumatology (Oxford) 2000;39:1180-1188
-
(2000)
Rheumatology (Oxford)
, vol.39
, pp. 1180-1188
-
-
Huizinga, T.W.1
Keijsers, V.2
Yanni, G.3
-
63
-
-
33646349199
-
Synovial membrane cytokine expression is predictive of joint damage progression in rheumatoid arthritis: A two-year prospective study (the DAMAGE study cohort)
-
Kirkham BW, Lassere MN, Edmonds JP, et al. Synovial membrane cytokine expression is predictive of joint damage progression in rheumatoid arthritis: A two-year prospective study (the DAMAGE study cohort). Arthritis Rheum 2006;54:1122-1131
-
(2006)
Arthritis Rheum
, vol.54
, pp. 1122-1131
-
-
Kirkham, B.W.1
Lassere, M.N.2
Edmonds, J.P.3
-
64
-
-
0037444072
-
Chronic synovitis and HLA B27 in patients with severe haemophilia
-
Ghosh K, Shankarkumar U, Shetty S, Mohanty D. Chronic synovitis and HLA B27 in patients with severe haemophilia. Lancet 2003;361:933-934
-
(2003)
Lancet
, vol.361
, pp. 933-934
-
-
Ghosh, K.1
Shankarkumar, U.2
Shetty, S.3
Mohanty, D.4
-
65
-
-
0035178886
-
Role of activatory Fc gamma RI and Fc gamma RIII and inhibitory Fc gamma RII in inflammation and cartilage destruction during experimental antigen-induced arthritis
-
van Lent PL, Nabbe K, Blom AB, et al. Role of activatory Fc gamma RI and Fc gamma RIII and inhibitory Fc gamma RII in inflammation and cartilage destruction during experimental antigen-induced arthritis. Am J Pathol 2001;159:2309-2320
-
(2001)
Am J Pathol
, vol.159
, pp. 2309-2320
-
-
van Lent, P.L.1
Nabbe, K.2
Blom, A.B.3
-
66
-
-
33646126521
-
Pathogenesis of haemophilic arthropathy
-
Roosendaal G, Lafeber FP. Pathogenesis of haemophilic arthropathy. Haemophilia 2006;12(Suppl 3):117-121
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 3
, pp. 117-121
-
-
Roosendaal, G.1
Lafeber, F.P.2
-
67
-
-
34447648526
-
Restoring hemostatic thrombin generation at the time of cutaneous wounding does not normalize healing in hemophilia B
-
McDonald A, Hoffman M, Hedner U, Roberts HR, Monroe DM. Restoring hemostatic thrombin generation at the time of cutaneous wounding does not normalize healing in hemophilia B. J Thromb Haemost 2007;5:1577-1583
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1577-1583
-
-
McDonald, A.1
Hoffman, M.2
Hedner, U.3
Roberts, H.R.4
Monroe, D.M.5
-
69
-
-
0034101945
-
Vascular endothelial growth factor production by fibroblasts in response to factor VIIa binding to tissue factor involves thrombin and factor Xa
-
Ollivier V, Chabbat J, Herbert JM, Hakim J, de Prost D. Vascular endothelial growth factor production by fibroblasts in response to factor VIIa binding to tissue factor involves thrombin and factor Xa. Arterioscler Thromb Vasc Biol 2000;20:1374-1381
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 1374-1381
-
-
Ollivier, V.1
Chabbat, J.2
Herbert, J.M.3
Hakim, J.4
de Prost, D.5
-
70
-
-
33644900978
-
Effect of heme and heme oxygenase-1 on vascular endothelial growth factor synthesis and angiogenic potency of human keratinocytes
-
Jazwa A, Loboda A, Golda S, et al. Effect of heme and heme oxygenase-1 on vascular endothelial growth factor synthesis and angiogenic potency of human keratinocytes. Free Radic Biol Med 2006;40:1250-1263
-
(2006)
Free Radic Biol Med
, vol.40
, pp. 1250-1263
-
-
Jazwa, A.1
Loboda, A.2
Golda, S.3
-
71
-
-
0032864718
-
Synovial cytokine and growth factor regulation of MMPs/TIMPs: Implications for erosions and angiogenesis in early rheumatoid and psoriatic arthritis patients
-
Fearon U, Reece R, Smith J, Emery P, Veale DJ. Synovial cytokine and growth factor regulation of MMPs/TIMPs: implications for erosions and angiogenesis in early rheumatoid and psoriatic arthritis patients. Ann N Y Acad Sci 1999;878:619-621
-
(1999)
Ann N Y Acad Sci
, vol.878
, pp. 619-621
-
-
Fearon, U.1
Reece, R.2
Smith, J.3
Emery, P.4
Veale, D.J.5
-
72
-
-
0347928884
-
High serum vascular endothelial growth factor correlates with disease activity of spondylarthropathies
-
Drouart M, Saas P, Billot M, et al. High serum vascular endothelial growth factor correlates with disease activity of spondylarthropathies. Clin Exp Immunol 2003;132:158-162
-
(2003)
Clin Exp Immunol
, vol.132
, pp. 158-162
-
-
Drouart, M.1
Saas, P.2
Billot, M.3
-
73
-
-
33846471735
-
VEGF, FGF1, FGF2 and EGF gene polymorphisms and psoriatic arthritis
-
Butt C, Lim S, Greenwood C, Rahman P. VEGF, FGF1, FGF2 and EGF gene polymorphisms and psoriatic arthritis. BMC Musculoskelet Disord 2007;8:1
-
(2007)
BMC Musculoskelet Disord
, vol.8
, pp. 1
-
-
Butt, C.1
Lim, S.2
Greenwood, C.3
Rahman, P.4
-
74
-
-
24144480556
-
Cytokine genotypes correlate with pain and radiologically defined joint damage in patients with juvenile rheumatoid arthritis
-
Oen K, Malleson PN, Cabral DA, et al. Cytokine genotypes correlate with pain and radiologically defined joint damage in patients with juvenile rheumatoid arthritis. Rheumatology (Oxford) 2005;44:1115-1121
-
(2005)
Rheumatology (Oxford)
, vol.44
, pp. 1115-1121
-
-
Oen, K.1
Malleson, P.N.2
Cabral, D.A.3
-
75
-
-
8844278362
-
A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans
-
Bond GL, Hu W, Bond EE, et al. A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans. Cell 2004;119:591-602
-
(2004)
Cell
, vol.119
, pp. 591-602
-
-
Bond, G.L.1
Hu, W.2
Bond, E.E.3
-
76
-
-
0031433062
-
Phenotype-genotype correlation in haemochromatosis subjects
-
Mura C, Nousbaum JB, Verger P, et al. Phenotype-genotype correlation in haemochromatosis subjects. Hum Genet 1997;101:271-276
-
(1997)
Hum Genet
, vol.101
, pp. 271-276
-
-
Mura, C.1
Nousbaum, J.B.2
Verger, P.3
-
77
-
-
35648973859
-
The H63D variant in the HFE gene predisposes to arthralgia, Chondrocalcinosis and osteoarthritis
-
Alizadeh BZ, Njajou OT, Hazes JM, et al. The H63D variant in the HFE gene predisposes to arthralgia, Chondrocalcinosis and osteoarthritis. Ann Rheum Dis 2007; 66:1436-1442
-
(2007)
Ann Rheum Dis
, vol.66
, pp. 1436-1442
-
-
Alizadeh, B.Z.1
Njajou, O.T.2
Hazes, J.M.3
-
78
-
-
17044402672
-
HFE mutations in the pathobiology of hemophilic arthropathy
-
Cruz E, Porto G, Morais S, Campos M, de Sousa M. HFE mutations in the pathobiology of hemophilic arthropathy. Blood 2005;105:3381-3382
-
(2005)
Blood
, vol.105
, pp. 3381-3382
-
-
Cruz, E.1
Porto, G.2
Morais, S.3
Campos, M.4
de Sousa, M.5
-
79
-
-
33846912561
-
Different clinical phenotype in triplets with haemophilia A
-
Barnes C, Blanchette V, Lillicrap D, et al. Different clinical phenotype in triplets with haemophilia A. Haemophilia 2007;13:202-205
-
(2007)
Haemophilia
, vol.13
, pp. 202-205
-
-
Barnes, C.1
Blanchette, V.2
Lillicrap, D.3
-
80
-
-
23044514669
-
Epigenetic differences arise during the lifetime of monozygotic twins
-
Fraga MF, Ballestar E, Paz MF, et al. Epigenetic differences arise during the lifetime of monozygotic twins. Proc Natl Acad Sci U S A 2005;102:10604-10609
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 10604-10609
-
-
Fraga, M.F.1
Ballestar, E.2
Paz, M.F.3
-
81
-
-
0030013165
-
Sports and hemophilia: Antagonist or protagonist
-
Buzzard BM. Sports and hemophilia: antagonist or protagonist. Clin Orthop Relat Res 1996;328:25-30
-
(1996)
Clin Orthop Relat Res
, vol.328
, pp. 25-30
-
-
Buzzard, B.M.1
-
82
-
-
0032979015
-
Body mass index, weight change, and incidence of self-reported physician-diagnosed arthritis among women
-
Sahyoun NR, Hochberg MC, Helmick CG, Harris T, Pamuk ER. Body mass index, weight change, and incidence of self-reported physician-diagnosed arthritis among women. Am J Public Health 1999;89:391-394
-
(1999)
Am J Public Health
, vol.89
, pp. 391-394
-
-
Sahyoun, N.R.1
Hochberg, M.C.2
Helmick, C.G.3
Harris, T.4
Pamuk, E.R.5
-
83
-
-
0037241181
-
Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A?
-
Ahmed R, Kannan M, Choudhry VP, Saxena R. Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A? Thromb Res 2003;109:71-72
-
(2003)
Thromb Res
, vol.109
, pp. 71-72
-
-
Ahmed, R.1
Kannan, M.2
Choudhry, V.P.3
Saxena, R.4
-
84
-
-
0035758034
-
Coexistence of a common prothrombotic risk factor and hemophilia in the Bulgarian hemophilic population:genotype/phenotype correlations
-
Petkova R, Chakarov S, Horvath A, Ganev V, Kremensky I. Coexistence of a common prothrombotic risk factor and hemophilia in the Bulgarian hemophilic population:genotype/phenotype correlations. Balkan J Med Genet 2001;4: 37-39
-
(2001)
Balkan J Med Genet
, vol.4
, pp. 37-39
-
-
Petkova, R.1
Chakarov, S.2
Horvath, A.3
Ganev, V.4
Kremensky, I.5
-
85
-
-
33746152007
-
Platelets as modifiers of clinical phenotype in hemophilia
-
Yee DL. Platelets as modifiers of clinical phenotype in hemophilia. Sci World J 2006;6:661-668
-
(2006)
Sci World J
, vol.6
, pp. 661-668
-
-
Yee, D.L.1
-
86
-
-
0028043709
-
-
Skogen B, Bellissimo DB, Hessner MJ, et al. Rapid determination of platelet alloantigen genotypes by polymerase chain reaction using allele-specific primers. Transfusion 1994;34:955-960
-
Skogen B, Bellissimo DB, Hessner MJ, et al. Rapid determination of platelet alloantigen genotypes by polymerase chain reaction using allele-specific primers. Transfusion 1994;34:955-960
-
-
-
-
87
-
-
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
-
Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. 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 1996;88:3698-3703
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
88
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BP, Koster T, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994;369:64-67
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.2
Koster, T.3
-
89
-
-
0031726760
-
Genetic modulation of coagulation factor VII plasma levels: Contribution of different polymorphisms and gender-related effects
-
Di Castelnuovo A, D'Orazio A, Amore C, et al. Genetic modulation of coagulation factor VII plasma levels: contribution of different polymorphisms and gender-related effects. Thromb Haemost 1998;80:592-597
-
(1998)
Thromb Haemost
, vol.80
, pp. 592-597
-
-
Di Castelnuovo, A.1
D'Orazio, A.2
Amore, C.3
-
90
-
-
0032532598
-
-
Kangsadalampai S, Board P. The Val34Leu polymorphism in the A subunit of coagulation factor XIII contributes to the large normal range in activity and demonstrates that the activation peptide plays a role in catalytic activity. Blood 1998;92:2766-2770
-
Kangsadalampai S, Board P. The Val34Leu polymorphism in the A subunit of coagulation factor XIII contributes to the large normal range in activity and demonstrates that the activation peptide plays a role in catalytic activity. Blood 1998;92:2766-2770
-
-
-
-
91
-
-
0038299177
-
Association between thrombin-activatable fibrinolysis inhibitor (TAFI) and clinical outcome in patients with unstable angina pectoris
-
Brouwers GJ, Leebeek FW, Tanck MW, Wouter Jukema J, Kluft C, de Maat MP. Association between thrombin-activatable fibrinolysis inhibitor (TAFI) and clinical outcome in patients with unstable angina pectoris. Thromb Haemost 2003;90:92-100
-
(2003)
Thromb Haemost
, vol.90
, pp. 92-100
-
-
Brouwers, G.J.1
Leebeek, F.W.2
Tanck, M.W.3
Wouter Jukema, J.4
Kluft, C.5
de Maat, M.P.6
-
92
-
-
0035657767
-
Prevalence of a 23bp insertion in exon 3 of the endothelial cell protein C receptor gene in venous thrombophilia
-
von Depka M, Czwalinna A, Eisert R, et al. Prevalence of a 23bp insertion in exon 3 of the endothelial cell protein C receptor gene in venous thrombophilia. Thromb Haemost 2001;86:1360-1362
-
(2001)
Thromb Haemost
, vol.86
, pp. 1360-1362
-
-
von Depka, M.1
Czwalinna, A.2
Eisert, R.3
-
93
-
-
33644973995
-
Polymorphism in the tissue factor region is associated with basal but not endotoxin-induced tissue factor-mRNA levels in leukocytes
-
Marsik C, Endler G, Halama T, et al. Polymorphism in the tissue factor region is associated with basal but not endotoxin-induced tissue factor-mRNA levels in leukocytes. J Thromb Haemost 2006;4:745-749
-
(2006)
J Thromb Haemost
, vol.4
, pp. 745-749
-
-
Marsik, C.1
Endler, G.2
Halama, T.3
-
94
-
-
0036626870
-
Endothelial nitric oxide synthase gene polymorphisms in Fabry's disease
-
Heltianu C, Costache G, Azibi K, Poenaru L, Simionescu M. Endothelial nitric oxide synthase gene polymorphisms in Fabry's disease. Clin Genet 2002;61:423-429
-
(2002)
Clin Genet
, vol.61
, pp. 423-429
-
-
Heltianu, C.1
Costache, G.2
Azibi, K.3
Poenaru, L.4
Simionescu, M.5
-
95
-
-
0141958654
-
Tissue plasminogen activator and plasminogen activator inhibitor type 1 gene polymorphism in patients with gastric ulcer complicated with bleeding
-
Kim HS, Hwang KY, Chung IK, et al. Tissue plasminogen activator and plasminogen activator inhibitor type 1 gene polymorphism in patients with gastric ulcer complicated with bleeding. J Korean Med Sci 2003;18:58-64
-
(2003)
J Korean Med Sci
, vol.18
, pp. 58-64
-
-
Kim, H.S.1
Hwang, K.Y.2
Chung, I.K.3
-
96
-
-
0037384474
-
Fibrinogen gene promoter -455 A allele as a risk factor for lacunar stroke
-
Martiskainen M, Pohjasvaara T, Mikkelsson J, et al. Fibrinogen gene promoter -455 A allele as a risk factor for lacunar stroke. Stroke 2003;34:886-891
-
(2003)
Stroke
, vol.34
, pp. 886-891
-
-
Martiskainen, M.1
Pohjasvaara, T.2
Mikkelsson, J.3
-
97
-
-
0035014293
-
Analysis of the tissue factor pathway inhibitor gene and antigen levels in relation to venous thrombosis
-
Amini-Nekoo A, Futers TS, Moia M, Mannucci PM, Grant PJ, Ariens R. Analysis of the tissue factor pathway inhibitor gene and antigen levels in relation to venous thrombosis. Br J Haematol 2001;113:537-543
-
(2001)
Br J Haematol
, vol.113
, pp. 537-543
-
-
Amini-Nekoo, A.1
Futers, T.S.2
Moia, M.3
Mannucci, P.M.4
Grant, P.J.5
Ariens, R.6
-
98
-
-
0028968010
-
Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk
-
Spek CA, Koster T, Rosendaal FR, Bertina RM, Reitsma P. Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk. Arterioscler Thromb Vasc Biol 1995;15: 214-218
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 214-218
-
-
Spek, C.A.1
Koster, T.2
Rosendaal, F.R.3
Bertina, R.M.4
Reitsma, P.5
-
99
-
-
0032874539
-
Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene
-
Leroy-Matheron C, Duchemin J, Levent M, Gouault-Heilmann M. Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene. Thromb Haemost 1999;82:1088-1092
-
(1999)
Thromb Haemost
, vol.82
, pp. 1088-1092
-
-
Leroy-Matheron, C.1
Duchemin, J.2
Levent, M.3
Gouault-Heilmann, M.4
-
100
-
-
0031775509
-
A mutation in the thrombomodulin gene, 127G to A coding for Ala25Thr, and the risk of myocardial infarction in men
-
Doggen CJ, Kunz G, Rosendaal FR, et al. A mutation in the thrombomodulin gene, 127G to A coding for Ala25Thr, and the risk of myocardial infarction in men. Thromb Haemost 1998;80:743-748
-
(1998)
Thromb Haemost
, vol.80
, pp. 743-748
-
-
Doggen, C.J.1
Kunz, G.2
Rosendaal, F.R.3
-
101
-
-
0026651907
-
Evidence, from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels
-
Tiret L, Rigat B, Visvikis S, et al. Evidence, from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels. Am J Hum Genet 1992;51:197-205
-
(1992)
Am J Hum Genet
, vol.51
, pp. 197-205
-
-
Tiret, L.1
Rigat, B.2
Visvikis, S.3
-
102
-
-
3042554701
-
Interleukin 1 beta and tumor necrosis factor levels in stored platelet concentrates and the association with gene polymorphisms
-
Addas-Carvalho M, Origa AF, Saad ST. Interleukin 1 beta and tumor necrosis factor levels in stored platelet concentrates and the association with gene polymorphisms. Transfusion 2004;44:996-1003
-
(2004)
Transfusion
, vol.44
, pp. 996-1003
-
-
Addas-Carvalho, M.1
Origa, A.F.2
Saad, S.T.3
-
103
-
-
0033670393
-
A polymorphism of the interleukin-1 beta gene influences survival in pancreatic cancer
-
Barber MD, Powell JJ, Lynch SF, Fearon KC. J.A. R. A polymorphism of the interleukin-1 beta gene influences survival in pancreatic cancer. Br J Cancer 2000;83:1443-1447
-
(2000)
Br J Cancer
, vol.83
, pp. 1443-1447
-
-
Barber, M.D.1
Powell, J.J.2
Lynch, S.F.3
Fearon, K.J.A.R.4
-
104
-
-
0027212397
-
Polymorphism in human IL-1 receptor antagonist gene intron 2 is caused by variable numbers of an 86-bp tandem repeat
-
Tarlow JK, Blakemore AI, Lennard A, et al. Polymorphism in human IL-1 receptor antagonist gene intron 2 is caused by variable numbers of an 86-bp tandem repeat. Hum Genet 1993;91:403-404
-
(1993)
Hum Genet
, vol.91
, pp. 403-404
-
-
Tarlow, J.K.1
Blakemore, A.I.2
Lennard, A.3
-
105
-
-
0026089188
-
Polymorphic structure of the tumor necrosis factor (TNF) locus: An NcoI polymorphism in the first intron of the human TNF-beta gene correlates with a variant amino acid in position 26 and a reduced level of TNF-beta production
-
Messer G, Spengler U, Jung MC, et al. Polymorphic structure of the tumor necrosis factor (TNF) locus: an NcoI polymorphism in the first intron of the human TNF-beta gene correlates with a variant amino acid in position 26 and a reduced level of TNF-beta production. J Exp Med 1991;173:209-219
-
(1991)
J Exp Med
, vol.173
, pp. 209-219
-
-
Messer, G.1
Spengler, U.2
Jung, M.C.3
-
106
-
-
0036892525
-
Host defense and inflammatory gene polymorphisms are associated with outcomes after HLA-identical sibling bone marrow transplantation
-
Rocha V, Franco RF, Porcher R, et al. Host defense and inflammatory gene polymorphisms are associated with outcomes after HLA-identical sibling bone marrow transplantation. Blood 2002;100:3908-3918
-
(2002)
Blood
, vol.100
, pp. 3908-3918
-
-
Rocha, V.1
Franco, R.F.2
Porcher, R.3
-
107
-
-
34548061536
-
Investigation of vascular endothelial growth factor gene polymorphisms and its association with clinicopathologic characteristics in gastric cancer
-
Chae YS, Kim JG, Sohn SK, et al. Investigation of vascular endothelial growth factor gene polymorphisms and its association with clinicopathologic characteristics in gastric cancer. Oncology 2006;71:266-272
-
(2006)
Oncology
, vol.71
, pp. 266-272
-
-
Chae, Y.S.1
Kim, J.G.2
Sohn, S.K.3
|