1 |
Gangat N, Wassie EA, Lasho TL, et al (2015). Mutations and thrombosis in essential thrombocythemia: prognostic interaction with age and thrombosis history. Eur J Haematol, 94, 31-6.
DOI
|
2 |
Hamidah NH, Farisah NR, Azlinda AB, et al (2012). A study of JAK2 (V617F) gene mutation in patients with chronic myeloproliferative disorders. Clin Ter, 163, 109-13.
|
3 |
Kiladjian JJ, Besses C, Griesshammer M, eta l (2013). Efficacy and safety of cytoreductive therapies in patients with essential thrombocythaemia aged >80 years: an interim analysis of the EXELS study. Clin Drug Investig,33,55-63.
DOI
|
4 |
Levine RL, Pardanani A, Tefferi A, Gilliland DG (2007). Role of JAK2 in the pathogenesis and therapy of myeloproliferative disorders. Nat Rev Cancer, 7, 673-83.
DOI
|
5 |
Palandri F, Latagliata R, Polverelli N, et al (2015). Mutations and long-term outcome of 217 young patients with essential thrombocythemia or early primary myelofibrosis. Leukemia, 29, 1344-9.
DOI
|
6 |
Payzin KB, Savasoglu K, Alacacioglu I, et al (2014). JAK2 V617F mutation status of 232 patients diagnosed with chronic myeloproliferative neoplasms. Clin Lymphoma Myeloma Leuk, 14, 525-33.
DOI
|
7 |
Ross C, Vanamala N, Rameshkumar (2008). Polycythemia Vera and Essential Thombocythemia-A Single Institution Experience. Indian J Med Paediatric Oncol, 29, 7-11.
DOI
|
8 |
Sadiq MA, Ahmed S, Ali N (2013). Frequency of Janus associated kinase 2 (JAK2) mutation in patients of BCRABL negative myeloproliferative neoplasms. Applied life sciences, 2, 235-40.
|
9 |
Sag SO, Gorukmez O, Ture M, et al (2015). MMP2 gene-735 C/T and MMP9 gene -1562 C/T polymorphisms in JAK2V617F positive myeloproliferative disorders. Asian Pac J Cancer Prev, 16, 443-9.
DOI
|
10 |
Sazawal S, Bajaj J, Chikkara S, et al (2010). Prevalence of JAK2 V617F mutation in Indian patients with chronic myeloproliferative disorders. Indian J Med Re, 132, 423-7.
|
11 |
Tefferi A, Barbui T (2015). Polycythemia vera and essential thrombocythemia: 2015 update on diagnosis, riskstratification and management. Am J Hematol, 90, 162-73.
DOI
|
12 |
Tefferi A (2013). Polycythemia vera and essential thrombocythemia: 2013 update on diagnosis, risk-stratification, and management. Am J Hematol, 88, 507-16.
DOI
|
13 |
Thiele J, Kvasnicka HM, Orazi A, et al (2008). WHO classification of tumours of haemopoietic and lymphoid tissues. Lyon: Int Agen Res Cancer, 48.
|
14 |
Varghese SJ, Bahey El, Din M, Al Hendi M, Kumar R (2013). Essential thrombocythaemia: a single institution experience of 16 years. Indian J Hematol Blood Transfu, 29, 139-46.
DOI
|
15 |
Yang JJ, Chen H, Zheng XQ, et al (2015). Methylated alteration of SHP1 complements mutation of JAK2 tyrosine kinase in patients with myeloproliferative neoplasm. Asian Pac J Cancer Prev, 16, 2219-25.
DOI
|
16 |
Yonal-Hindilerden I, Daglar-Aday A, Akadam-Teker B, et al (2015). The burden of JAK2V617F mutated Aallele in Turkish patients with myeloproliferative neoplasms. J Clin Med Res, 7, 161-70.
DOI
|
17 |
Zhang ZR, Duan YC (2014). Interferon apha 2b for treating patients with JAK2V617F positive polycythemia vera and essential thrombocytosis. Asian Pac J Cancer Prev, 15, 1681-4.
DOI
|
18 |
Ayad MW, Nafea D (2011). Acquired mutation of the tyrosine kinase JAK2V617F in Egyptian patients with myeloid disorders. Genet Test Mol Biomarkers, 15, 17-21.
DOI
|
19 |
Ahn JY, Yoo SJ, Bang SM, et al (2007). JAK2(V617F) mutation in Korean patients with essential thrombocythemia. Korean J Lab Med, 27, 77-82.
DOI
|
20 |
Alshemmari SH, Rajaan R, Ameen R, Al-Drees MA, Almosailleakh MR (2014). JAK2V617F allele burden in patients with myeloproliferative neoplasms. Ann Hematol, 93, 791-6.
DOI
|
21 |
Ben Said M, Gandrille S, Fischer AM, Darnige L (2015). Clinical and biological features of patients with essential thrombocythaemia according to their mutational status JAK2 or CALR: Single-center study of 40 patients and review of the literature. Pathol Biol (Paris), 63, 117-21.
DOI
|
22 |
Briere JB (2007). Essential thrombocythemia. Orphanet J Rare Dis, 2, 3.
DOI
|
23 |
Birgegard G (2015). Advances and challenges in the management of essential thrombocythemia. Ther Adv Hematol, 6, 142-56.
DOI
|
24 |
Duangnapasatit B, Rattarittamrong E, Rattanathammethee T, et al (2015). Clinical manifestations and risk factors for complications of Philadelphia chromosome-negative myeloproliferative neoplasms. Asian Pac J Cancer Prev, 16, 5013-8.
DOI
|