Results 121 to 130 of about 3,126,313 (204)
Essential thrombocythemia (ET) is a Philadelphia-negative chronic myeloproliferative neoplasm characterized by acquired somatic mutations: JAK2, CALR or MPL.
A. Găman +3 more
semanticscholar +1 more source
BCR/ABL positive thrombocythemia: a diagnostic dilemma
Both chronic myeloid leukemia and essential thrombocythemia are part of the spectrum of myeloproliferative neoplasm. Therefore, considerable overlap may occur in the clinical manifestations, and hematological and molecular findings in some patients.
Lubna Zafar +3 more
doaj +1 more source
Fedratinib (SAR302503, TG101348) is an orally administered Janus kinase (JAK) 2-selective inhibitor that is being developed for the treatment of patients with myelofibrosis (MF).
K. Ogasawara +4 more
semanticscholar +1 more source
Komplex molekuláris genetikai vizsgálati algoritmus myeloproliferativ neoplasiák diagnosztikájában [PDF]
Introduction: Mutations in Janus kinase 2, calreticulin and thrombopoietin receptor genes have been identified in the genetic background of Philadelphia chromosome negative, "classic" myeloproliferative neoplasms.
Andrikovics, Hajnalka +12 more
core +1 more source
Essential thrombocythemia presenting as digital ischemia
Essential thrombocythemia is a myeloproliferative disease and is characterized by increased production of platelet and increased megakaryocytes in the bone marrow.
Md. Nazmul Hasan +5 more
doaj +1 more source
Non ST-segment elevation myocardial infarction in patient with essential thrombocythemia
A 68-year-old woman presented with acute chest pain and a greatly increased platelet count. Cardiac catheterization revealed subtotal occlusion and a thrombus-like filling defect in the right coronary artery.
Tengiz Istemihan +8 more
doaj +1 more source
Enhanced platelet adhesion in essential thrombocythemia after in vitro activation [PDF]
Objective: Essential thrombocythemia (ET) is a chronic myeloproliferative disorder characterized by elevated platelet counts and increased risk of thrombosis.
Andreas C. Eriksson +2 more
core
Estudio molecular en Neoplasias Mieloproliferativas Crónicas: mutación JAK2V617F [PDF]
La mutación JAK2V617F constituye la alteración molecular más frecuente en Neoplasias Mieloproliferativas Crónicas BCR-ABL-negativas, detectándose en > 95% de los pacientes con Policitemia Vera y alrededor de 50-60% de aquellos con Mielofibrosis Primaria ...
Heller, Paula Graciela +1 more
core +1 more source
Chilblains as a Clue for the Diagnosis of Essential Thrombocythemia
N ...
Hugo J. Leme, José Ramos, Ângela Roda
doaj +1 more source
Influència de l'haplotip 46/1 del gen JAK2 en la variació de la càrrega al·lèlica de la mutació JAK2V617F en pacients amb policitèmia vera i trombocitèmia esencial [PDF]
La presència de l'haplotip 46/1 del gen JAK2 predisposa a neoplàsies mieloproliferatives associades a la mutació de JAK2V617F, però la seva rellevància clínica és desconeguda.
Angona i Figueras, Anna +3 more
core

