-
1
-
-
0033999779
-
Cause of portal or hepatic vein thrombosis in adults: the role of multiple concurrent factors
-
Denninger M.H., Chait Y., Casadevall N., et al. Cause of portal or hepatic vein thrombosis in adults: the role of multiple concurrent factors. Hepatology 31 (2000) 587-591
-
(2000)
Hepatology
, vol.31
, pp. 587-591
-
-
Denninger, M.H.1
Chait, Y.2
Casadevall, N.3
-
2
-
-
14244261724
-
Risk factors for thrombophilia in extrahepatic protal vein obstruction
-
Primignani M., Martinelli I., and Bucciarelli P. Risk factors for thrombophilia in extrahepatic protal vein obstruction. Hepatology 41 (2005) 603-608
-
(2005)
Hepatology
, vol.41
, pp. 603-608
-
-
Primignani, M.1
Martinelli, I.2
Bucciarelli, P.3
-
3
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative diseases
-
Baxter E.J., Scott L.M., Campbell P.J., et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative diseases. Lancet 365 (2005) 1054-1061
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
-
4
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
-
Levine R.L., Wadleigh M., Cools J., et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell 7 (2005) 387-397
-
(2005)
Cancer Cell
, vol.7
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
-
5
-
-
17844383458
-
Unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James C., Ugo V., Le Couedic J.P., et al. Unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 434 (2005) 1144-1148
-
(2005)
Nature
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couedic, J.P.3
-
6
-
-
17644424955
-
A gain-of function mutation of JAK2 in myeloproliferative disorders
-
Kralovics R., Passamonti F., Buser A.S., et al. A gain-of function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 352 (2005) 1779-1790
-
(2005)
N Engl J Med
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
-
7
-
-
34247876210
-
Quantitative determination of JAK2 V617F by TaqManan absolute measure of averaged copies per cell that reflects myeloproliferation
-
Hammond E., Shaw K., Carnley B., et al. Quantitative determination of JAK2 V617F by TaqManan absolute measure of averaged copies per cell that reflects myeloproliferation. J Mol Diagn 9 (2007) 242-248
-
(2007)
J Mol Diagn
, vol.9
, pp. 242-248
-
-
Hammond, E.1
Shaw, K.2
Carnley, B.3
-
8
-
-
33744490974
-
Expression of JAK2 V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model
-
Wernig G., Mercher T., Okabe R., et al. Expression of JAK2 V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model. Blood 107 (2006) 4274-4281
-
(2006)
Blood
, vol.107
, pp. 4274-4281
-
-
Wernig, G.1
Mercher, T.2
Okabe, R.3
-
9
-
-
33845630695
-
Role of the JAK2 mutation in the diagnosis of chronic myeloproliferative disorders in splanchnic vein thrombosis
-
Primignani M., Barosi G., Bergamaschi G., et al. Role of the JAK2 mutation in the diagnosis of chronic myeloproliferative disorders in splanchnic vein thrombosis. Hepatology 44 (2006) 1528-1534
-
(2006)
Hepatology
, vol.44
, pp. 1528-1534
-
-
Primignani, M.1
Barosi, G.2
Bergamaschi, G.3
-
10
-
-
33744505451
-
Prevalence of the activation JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome
-
Patel R.K., Lea N.C., Heneghan M.A., et al. Prevalence of the activation JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome. Gastroenterology 130 (2006) 2013-2038
-
(2006)
Gastroenterology
, vol.130
, pp. 2013-2038
-
-
Patel, R.K.1
Lea, N.C.2
Heneghan, M.A.3
-
11
-
-
41149134046
-
-
Miescher P.A., Jaffe E.R., Beris P., et al. (Eds)
-
In: Miescher P.A., Jaffe E.R., Beris P., et al. (Eds). Polycythemia vera. Semin Hematol 34 (1997) 1-80
-
(1997)
Polycythemia vera. Semin Hematol
, vol.34
, pp. 1-80
-
-
-
12
-
-
0003477486
-
-
Jaffe E.S., Harris N.L., Stein H., et al. (Eds), IARC Press, Lyon, France
-
In: Jaffe E.S., Harris N.L., Stein H., et al. (Eds). World Health Organization classification of tumours: pathology and genetics of tumours of haematopoietic and lymphoid tissues (2001), IARC Press, Lyon, France
-
(2001)
World Health Organization classification of tumours: pathology and genetics of tumours of haematopoietic and lymphoid tissues
-
-
-
13
-
-
37749046766
-
Classification, diagnosis and management of myeloproliferative disorders in the JAK2 V617F Era
-
www.asheducationbook.org
-
Tefferi A. Classification, diagnosis and management of myeloproliferative disorders in the JAK2 V617F Era. ASH Education Book (2006) 240-245. http://www.asheducationbook.org www.asheducationbook.org
-
(2006)
ASH Education Book
, pp. 240-245
-
-
Tefferi, A.1
-
14
-
-
28244442441
-
Definition of subtypes of essential thrombocythaemia and relation to polycythemia vera based on JAK2 V617F mutation status: a prospective study
-
Campbell P.J., Scott L.M., Buck G., et al. Definition of subtypes of essential thrombocythaemia and relation to polycythemia vera based on JAK2 V617F mutation status: a prospective study. Lancet 366 (2005) 1945-1953
-
(2005)
Lancet
, vol.366
, pp. 1945-1953
-
-
Campbell, P.J.1
Scott, L.M.2
Buck, G.3
-
15
-
-
30844444135
-
The JAK2 tyrosine kinase mutation in myelofibrosis with myeloid metaplasia: lineage specificity and clinical correlates
-
Tefferi A., Lasho T.L., Schwager S.M., et al. The JAK2 tyrosine kinase mutation in myelofibrosis with myeloid metaplasia: lineage specificity and clinical correlates. Br J Haematol 131 (2005) 320-328
-
(2005)
Br J Haematol
, vol.131
, pp. 320-328
-
-
Tefferi, A.1
Lasho, T.L.2
Schwager, S.M.3
-
16
-
-
27744606173
-
JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance
-
Wolanskyj A.P., Lasho T.L., Schwager S.M., et al. JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance. Br J Haematol 131 (2005) 208-213
-
(2005)
Br J Haematol
, vol.131
, pp. 208-213
-
-
Wolanskyj, A.P.1
Lasho, T.L.2
Schwager, S.M.3
-
17
-
-
33344471678
-
V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis
-
Campell P., Griesshammer M., Dohner K., et al. V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis. Blood 107 (2006) 2098-2100
-
(2006)
Blood
, vol.107
, pp. 2098-2100
-
-
Campell, P.1
Griesshammer, M.2
Dohner, K.3
|