-
1
-
-
27944450847
-
Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs
-
Almawi WY, Keleshian SH, Borgi L et al (2005) Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs. J Thromb Thrombolys 20:163-168
-
(2005)
J Thromb Thrombolys
, vol.20
, pp. 163-168
-
-
Almawi, W.Y.1
Keleshian, S.H.2
Borgi, L.3
-
2
-
-
0347418229
-
Hypercoagulability in sickle cell disease: A curious paradox
-
Ataga KI, Orringer EP (2003) Hypercoagulability in sickle cell disease: a curious paradox. Am J Med 115:721-728
-
(2003)
Am J Med
, vol.115
, pp. 721-728
-
-
Ataga, K.I.1
Orringer, E.P.2
-
3
-
-
32144445778
-
Plasma lipids in Iranians with sickle cell disease: Hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait
-
Rahimi Z, Merat A, Haghshenass M, Madani H, Rezaei M, Nagel RL (2006) Plasma lipids in Iranians with sickle cell disease: Hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait. Clin Chim Acta 365:217-220
-
(2006)
Clin Chim Acta
, vol.365
, pp. 217-220
-
-
Rahimi, Z.1
Merat, A.2
Haghshenass, M.3
Madani, H.4
Rezaei, M.5
Nagel, R.L.6
-
5
-
-
23944506662
-
Should we screen Eastern Mediterranean sickle beta-thalassemia patients for inherited thrombophilia?
-
Otrock ZK, Mahfouz RAR, Taher AT (2005) Should we screen Eastern Mediterranean sickle beta-thalassemia patients for inherited thrombophilia? J Thromb Haemost 3:599-600
-
(2005)
J Thromb Haemost
, vol.3
, pp. 599-600
-
-
Otrock, Z.K.1
Mahfouz, R.A.R.2
Taher, A.T.3
-
6
-
-
33749186021
-
Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-beta-0-thalassemia patients
-
Isma'eel H, Shamseddeen AW, Mahfouz R, Zeineh N, Jradi O, Taher A (2006) Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-beta-0-thalassemia patients. J Thromb Thrombolys 22:121-123
-
(2006)
J Thromb Thrombolys
, vol.22
, pp. 121-123
-
-
Isma'eel, H.1
Shamseddeen, A.W.2
Mahfouz, R.3
Zeineh, N.4
Jradi, O.5
Taher, A.6
-
7
-
-
0031825212
-
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil
-
Andrade FL, Annichino-Bizzacchi JM, Saad STO, Costa FF, Arruda VR (1998) Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil. Am J Hematol 59:46-50
-
(1998)
Am J Hematol
, vol.59
, pp. 46-50
-
-
Andrade, F.L.1
Annichino-Bizzacchi, J.M.2
Saad, S.T.O.3
Costa, F.F.4
Arruda, V.R.5
-
8
-
-
3042646355
-
Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia
-
Fawaz NA, Bashawery L, Al-Sheikh I, Qatari A, Al-Othman SS, Almawi WY (2004) Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia. Am J Hematol 76:307-309
-
(2004)
Am J Hematol
, vol.76
, pp. 307-309
-
-
Fawaz, N.A.1
Bashawery, L.2
Al-Sheikh, I.3
Qatari, A.4
Al-Othman, S.S.5
Almawi, W.Y.6
-
9
-
-
0002804061
-
Biochemical aspects of hematology
-
In: Burtis CA, Ashwood ER (eds) W.B.Saunders, Philadelphia
-
Fairbanks VF, Klee GG (1994) Biochemical aspects of hematology. In: Burtis CA, Ashwood ER (eds) Tietz text book of clinical chemistry. W.B.Saunders, Philadelphia, pp 2041-2042
-
(1994)
Tietz Text Book of Clinical Chemistry
, pp. 2041-2042
-
-
Fairbanks, V.F.1
Klee, G.G.2
-
10
-
-
0002804385
-
Gene analysis
-
In: Weatherall DJ (ed) Churchill Livingstone, London
-
Old JM, Higgs DR (1983) Gene analysis. In: Weatherall DJ (ed) Methods in hematology. The thalassemias, vol 6. Churchill Livingstone, London, pp 74-101
-
(1983)
Methods in Hematology. The Thalassemias
, vol.6
, pp. 74-101
-
-
Old, J.M.1
Higgs, D.R.2
-
11
-
-
0028158097
-
Reverse dot blot probes for the screening of β-thalassemia mutations in Asian and American Blacks
-
Cai SP, Wall J, Kan WY, Chehab FF (1994) Reverse dot blot probes for the screening of β-thalassemia mutations in Asian and American Blacks. Hum Mutat 3:59-63
-
(1994)
Hum Mutat
, vol.3
, pp. 59-63
-
-
Cai, S.P.1
Wall, J.2
Kan, W.Y.3
Chehab, F.F.4
-
12
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koster T et al (1994) Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 369:64-67
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
-
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
-
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
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
14
-
-
0031724415
-
Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease
-
Zimmerman SA, Ware RE (1998) Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease. Am J Hematol 59:267-272
-
(1998)
Am J Hematol
, vol.59
, pp. 267-272
-
-
Zimmerman, S.A.1
Ware, R.E.2
-
15
-
-
0033976036
-
Thrombophilic Mutations in Iran
-
Zeinali S, Duca F, Zarbakhsh B, Tagliabue L, Mannucci PM (2000) Thrombophilic Mutations in Iran. Thromb Haemost 83:351-352
-
(2000)
Thromb Haemost
, vol.83
, pp. 351-352
-
-
Zeinali, S.1
Duca, F.2
Zarbakhsh, B.3
Tagliabue, L.4
Mannucci, P.M.5
-
16
-
-
0036631123
-
Recurrent thromboembolism in a patient with β-thalassemia major associated with double heterozygosity for factor V R506Q and prothrombin G20210A mutations
-
Kahn JE, Veyssier-Belot C, Renier JL, de Mazancourt P, Peltier JY, de Raucourt E (2002) Recurrent thromboembolism in a patient with β-thalassemia major associated with double heterozygosity for factor V R506Q and prothrombin G20210A mutations. Blood Coagul Fibrin 13:461-463
-
(2002)
Blood Coagul Fibrin
, vol.13
, pp. 461-463
-
-
Kahn, J.E.1
Veyssier-Belot, C.2
Renier, J.L.3
de Mazancourt, P.4
Peltier, J.Y.5
de Raucourt, E.6
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