Results 21 to 30 of about 23,927 (264)

JAK2 V617F Analysis in Indonesian Myeloproliferative Neoplasms Patients [PDF]

, 2015
Background : Three subtypes of myeloproliferative neoplasms (MPNs): Polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF) showed overlapping phenotype.
Faradz, S. M. (Sultana), Saktini, F. (Fanti), Santosa, S. (Santosa)   +2 more
core   +3 more sources

Distinguishing essential thrombocythemia JAK2V617F from polycythemia vera: limitations of erythrocyte values

Haematologica, 2019
Distinguishing essential thrombocythemia JAK2V617F from polycythemia vera is difficult because of shared mutation and phenotypic characteristics. The World Health Organization suggested hemoglobin and hematocrit values to diagnose polycythemia vera (PV),
Richard T. Silver, Spencer Krichevsky
doaj   +1 more source

Recurrent thrombosis of splanchnic and lower extremity arteries with essential thrombocythemia

SAGE Open Medical Case Reports, 2019
Essential thrombocythemia is a myeloproliferative neoplasm characterized by platelet aggregation and thrombosis. Clinically, essential thrombocythemia increases the risk of both thrombosis and bleeding. Essential thrombocythemia is more involved in micro-
Sung Min Jung, Heungman Jun
doaj   +1 more source

Pregnancy with Essential Thrombocythemia: A Case Report

Taiwanese Journal of Obstetrics & Gynecology, 2004
Objective: We describe a woman with essential thrombocythemia (ET) who experienced a successful pregnancy with no specific treatment. Case Report: A 30-year-old primiparous female was incidentally found to have ET with no specific symptoms at a ...
Yin-Jou Chou, Yu-Che Ou, Shiuh-Young Chang, Te-Yao Hsu   +3 more
doaj   +1 more source

Role of blood cells dynamism on hemostatic complications in low-risk patients with essential thrombocythemia [PDF]

, 2015
Patients with essential thrombocythemia (ET) aged less than 60 years, who have not suffered a previous vascular event (low-risk patients), may develop thrombotic or hemorrhagic events.
Bassan, Renato, Bertozzi, Irene, Bl\uf6chl, Elisabeth Maria, Cortelazzo, Sergio, Corvetta, Daisy, De Biasi, Ercole, Elli, Elena, Gastl, G\ufcnther, Gherlinzoni, Filippo, Gottardi, Michele, Guella, Anna, Innella, Barbara, Krampera, Mauro, Marabese, Alessandra, Marcheselli, Luigi, Mitterer, Manfred, Pacquola, Enrica, Perbellini, Omar, Piccin, Andrea, Pizzolo, Giovanni, Pogliani, Enrico Maria, Pusceddu, Irene, Randi, Maria Luigia, Rocconi, Roberta, Sancetta, Rosaria, Steurer, Michael, Tiribelli, Mario, Veneri, Dino, Vivaldi, Paolo   +28 more
core   +1 more source

Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms [PDF]

, 2015
Clonal proliferation in myeloproliferative neoplasms (MPN) is driven by somatic mutations in JAK2, CALR or MPL, but the contribution of inherited factors is poorly characterized. Using a three-stage genome-wide association study of 3,437 MPN cases and 10,
Aranaz, P., Aranaz, P., Bandinelli, S., Bandinelli, S., Barosi, G., Barosi, G., Baxter, E.J., Baxter, E.J., Callaway, A., Callaway, A., Campbell P., Campbell P., Cazzola, M., Cazzola, M., Chase, A., Chase, A., Chen, E., Chen, E., Cross N.C., Cross N.C., Dohner, K., Dohner, K., Duncombe, A.S., Duncombe, A.S., Evans, P., Evans, P., Ewing, J., Ewing, J., Gale, R.E., Gale, R.E., Giannopoulos, A., Giannopoulos, A., Gisslinger, H., Gisslinger, H., Godfrey, A.L., Godfrey, A.L., Grallert, H., Grallert, H., Green, A.R., Green, A.R., Griffiths, M., Griffiths, M., Guglielmelli, P., Guglielmelli, P., Haferlach, T., Haferlach, T., Harrison, C., Harrison, C., Harutyunyan, A.S., Harutyunyan, A.S., Jack, A., Jack, A., Jones, A.V., Jones, A.V., Kralovics, R., Kralovics, R., Leung, W., Leung, W., Lin, F., Lin, F., Maclean, C., Maclean, C., Mannarelli, C., Mannarelli, C., Mead, A.J., Mead, A.J., Nangalia, J., Nangalia, J., Oscier, D., Oscier, D., Pieri, L., Pieri, L., Reiter, A., Reiter, A., Schnittger, S., Schnittger, S., Schuh, A., Schuh, A., Short, M., Short, M., Stegelmann, F., Stegelmann, F., Strauch, K., Strauch, K., Tanaka, T., Tanaka, T., Tapper, W., Tapper, W., Vannucchi, A., Vannucchi, A., Waghorn, K., Waghorn, K., Wallis, L., Wallis, L., Ward, D., Ward, D., White, H.E., White, H.E., Zoi, K., Zoi, K.   +99 more
core   +5 more sources

Abnormal regulation of soluble and anchored IL-6 receptor in monocytes from patients with essential thrombocythemia [PDF]

, 2010
Objective: In a previous study, we found increased plasma soluble receptor for interleukin-6 (sIL-6R) levels in patients with essential thrombocythemia (ET) that could promote megakaryopoiesis through IL-6 binding and further interaction with the signal ...
Alvarez-Larrán, Ana C. Glembotsky, Arellano-Rodrigo, Barillé, Bauer, Baxter, Briso, Carlos D. Chazarreta, Chomczynski, Coles, Felisa C. Molinas, Gallea-Robache, Horiuchi, Jones, Jones, Jones, Jones, Jones, Juan P. Salim, Kralovics, Labbaye, Levine, Levine, Marta, Marta, Matthews, Mitsuyama, Mudter, Mullberg, Murakami-Mori, Murphy, Müllberg, Nakanishi, Nakashima, Nora P. Goette, Pang, Paola R. Lev, Pardanani, Park, Paula G. Heller, Rameshwar, Rosana F. Marta, Rose-John, Sui, Trikha, Varghese, Waetzig, Zheng   +47 more
core   +1 more source

Essential Thrombocythemia

JAMA
ImportanceEssential thrombocythemia, a clonal myeloproliferative neoplasm with excessive platelet production, is associated with an increased risk of thrombosis and bleeding. The annual incidence rate of essential thrombocythemia in the US is 1.5/100 000 persons.ObservationsPatients with essential thrombocythemia have a persistent platelet count of 450 
Ayalew, Tefferi, Naseema, Gangat, Giuseppe Gaetano, Loscocco, Paola, Guglielmelli, Natasha, Szuber, Animesh, Pardanani, Attilio, Orazi, Tiziano, Barbui, Alessandro Maria, Vannucchi   +8 more
  +6 more sources

A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family

Haematologica, 2008
Background Hereditary thrombocythemia is an autosomal dominant disorder with clinical features resembling sporadic essential thrombocythemia.
Kun Liu, Robert Kralovics, Zbigniew Rudzki, Barbara Grabowska, Andreas S. Buser, Damla Olcaydu, Heinz Gisslinger, Ralph Tiedt, Patricia Frank, Krzysztof Okoñ, Anthonie P.C. van der Maas, Radek C. Skoda   +11 more
doaj   +1 more source

A Case of Symptomatic Intraluminal Internal Carotid Artery Thrombus in a Patient with Essential Thrombocythemia Surgically Treated by CEA

Case Reports in Neurological Medicine, 2023
We report a patient with a symptomatic intraluminal internal carotid artery thrombus clinically revealed by cerebral infarction. In the preoperative evaluation, it was revealed that essential thrombocythemia existed in the background.
Satoshi Takahashi, Masahiro Katsumata, Hirotsugu Nogawa, Kento Takahara, Jin Nakahara, Masahiro Toda   +5 more
doaj   +1 more source