-
1
-
-
34250743644
-
Gain-of-function gene mutations and venous thromboembolism: Distinct roles in different clinical settings
-
Colaizzo, D., Amitrano, L., Iannaccone, L., Vergura, P., Cappucci, F., Grandone, E., Guardascione, M.A. Margaglione, M. (2007) Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings. Journal of Medical Genetics, 44, 412 416.
-
(2007)
Journal of Medical Genetics
, vol.44
, pp. 412-416
-
-
Colaizzo, D.1
Amitrano, L.2
Iannaccone, L.3
Vergura, P.4
Cappucci, F.5
Grandone, E.6
Guardascione, M.A.7
Margaglione, M.8
-
2
-
-
55049131023
-
Is JAK2 V617F mutation more than a diagnostic index? A meta-analysis of clinical outcomes in essential thrombocythemia
-
Dahabreh, I.J., Zoi, K., Giannouli, S., Zoi, C., Loukopoulos, D. Voulgarelis, M. (2009) Is JAK2 V617F mutation more than a diagnostic index? A meta-analysis of clinical outcomes in essential thrombocythemia. Leukemia Research, 33, 67 73.
-
(2009)
Leukemia Research
, vol.33
, pp. 67-73
-
-
Dahabreh, I.J.1
Zoi, K.2
Giannouli, S.3
Zoi, C.4
Loukopoulos, D.5
Voulgarelis, M.6
-
3
-
-
34147156839
-
Incidence of the JAK2 V617F mutation among patients with splanchnic or cerebral venous thrombosis and without overt chronic myeloproliferative disorders
-
De Stefano, V., Fiorini, A., Rossi, E., Za, T., Farina, G., Chiusolo, P., Sica, S. Leone, G. (2007) Incidence of the JAK2 V617F mutation among patients with splanchnic or cerebral venous thrombosis and without overt chronic myeloproliferative disorders. Journal of Thrombosis and Haemostasis, 5, 708 714.
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, pp. 708-714
-
-
De Stefano, V.1
Fiorini, A.2
Rossi, E.3
Za, T.4
Farina, G.5
Chiusolo, P.6
Sica, S.7
Leone, G.8
-
4
-
-
42149140574
-
JAK2V617F mutation screening as part of the hypercoagulable work-up in the absence of splanchnic venous thrombosis or overt myeloproliferative neoplasm: Assessment of value in a series of 664 consecutive patients
-
Pardanani, A., Lasho, T.L., Hussein, K., Schwager, S., Finke, C., Hussein, K., Pruthi, R.K. Tefferi, A. (2008) JAK2V617F mutation screening as part of the hypercoagulable work-up in the absence of splanchnic venous thrombosis or overt myeloproliferative neoplasm: assessment of value in a series of 664 consecutive patients. Mayo Clinic Proceedings, 83, 457 459.
-
(2008)
Mayo Clinic Proceedings
, vol.83
, pp. 457-459
-
-
Pardanani, A.1
Lasho, T.L.2
Hussein, K.3
Schwager, S.4
Finke, C.5
Hussein, K.6
Pruthi, R.K.7
Tefferi, A.8
-
5
-
-
34147152904
-
JAK2 V617F is specifically associated with idiopathic splanchnic vein thrombosis
-
Regina, S., Herault, O., D'Alteroche, L., Binet, C. Gruel, Y. (2007) JAK2 V617F is specifically associated with idiopathic splanchnic vein thrombosis. Journal of Thrombosis and Haemostasis, 5, 859 861.
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, pp. 859-861
-
-
Regina, S.1
Herault, O.2
D'Alteroche, L.3
Binet, C.4
Gruel, Y.5
-
6
-
-
33947529214
-
The V617F mutation of JAK2 is very uncommon in patients with thrombosis
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Remacha, A.F., Estivill, C., Sarda, M.P., Mateo, J., Souto, J.C., Canals, C., Nomdedéu, J. Fontcuberta, J. (2007) The V617F mutation of JAK2 is very uncommon in patients with thrombosis. Haematologica, 92, 285 286.
-
(2007)
Haematologica
, vol.92
, pp. 285-286
-
-
Remacha, A.F.1
Estivill, C.2
Sarda, M.P.3
Mateo, J.4
Souto, J.C.5
Canals, C.6
Nomdedéu, J.7
Fontcuberta, J.8
-
7
-
-
34548154461
-
JAK2V617F in idiopathic venous thromboembolism occurring in the absence of inherited or acquired thrombophilia
-
Rossi, D., Cresta, S., Destro, T., Vendramin, C., Bocchetta, S., De Paoli, L., Cerri, M., Lunghi, M. Gaidano, G. (2007) JAK2V617F in idiopathic venous thromboembolism occurring in the absence of inherited or acquired thrombophilia. British Journal of Haematology, 138, 813 814.
-
(2007)
British Journal of Haematology
, vol.138
, pp. 813-814
-
-
Rossi, D.1
Cresta, S.2
Destro, T.3
Vendramin, C.4
Bocchetta, S.5
De Paoli, L.6
Cerri, M.7
Lunghi, M.8
Gaidano, G.9
-
8
-
-
34548042964
-
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: Recommendations from an ad hoc international expert panel
-
Tefferi, A., Thiele, J., Orazi, A., Kvasnicka, H.M., Barbui, T., Hanson, C.A., Barosi, G., Verstovsek, S., Birgegard, G., Mesa, R., Reilly, J.T., Gisslinger, H., Vannucchi, A.M., Cervantes, F., Finazzi, G., Hoffman, R., Gilliland, D.G., Bloomfield, C.D. Vardiman, J.W. (2007) Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel. Blood, 110, 1092 1097.
-
(2007)
Blood
, vol.110
, pp. 1092-1097
-
-
Tefferi, A.1
Thiele, J.2
Orazi, A.3
Kvasnicka, H.M.4
Barbui, T.5
Hanson, C.A.6
Barosi, G.7
Verstovsek, S.8
Birgegard, G.9
Mesa, R.10
Reilly, J.T.11
Gisslinger, H.12
Vannucchi, A.M.13
Cervantes, F.14
Finazzi, G.15
Hoffman, R.16
Gilliland, D.G.17
Bloomfield, C.D.18
Vardiman, J.W.19
-
9
-
-
37549059954
-
Prevalence of the JAK2 V617F mutation is low among unselected patients with a first episode of unprovoked venous thromboembolism
-
for the EDITH Collaborative Study Group (
-
Ugo, V., Le Gal, G., Lecucq, L., Mottier, D. Oger, E. for the EDITH Collaborative Study Group (2008) Prevalence of the JAK2 V617F mutation is low among unselected patients with a first episode of unprovoked venous thromboembolism. Journal of Thrombosis and Haemostasis, 6, 203 205.
-
(2008)
Journal of Thrombosis and Haemostasis
, vol.6
, pp. 203-205
-
-
Ugo, V.1
Le Gal, G.2
Lecucq, L.3
Mottier, D.4
Oger, E.5
-
10
-
-
34548136101
-
Prospective identification of high-risk polycythemia vera patients based on JAK2 V617F allele burden
-
for the MPD Research Consortium (
-
Vannucchi, A.M., Antonioli, E., Guglielmelli, P., Longo, G., Pancrazzi, A., Ponziani, V., Bogani, C., Rossi Ferrini, P., Rambaldi, A., Guerini, V., Bosi, A. Barbui, T. for the MPD Research Consortium (2007) Prospective identification of high-risk polycythemia vera patients based on JAK2 V617F allele burden. Leukemia, 21, 1952 1959.
-
(2007)
Leukemia
, vol.21
, pp. 1952-1959
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
Longo, G.4
Pancrazzi, A.5
Ponziani, V.6
Bogani, C.7
Rossi Ferrini, P.8
Rambaldi, A.9
Guerini, V.10
Bosi, A.11
Barbui, T.12
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