نتایج جستجو برای: myeloproliferative disorder

تعداد نتایج: 601334  

Journal: :international journal of hematology-oncology and stem cell research 0
majid vafaie research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. kaveh jaseb research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. majid ghanavat research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. mohamad pedram research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran. tooran rahiminia research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran.

essential thrombocythemia is a rare myeloproliferative disorder in pediatrics. this myeloproliferative disorder is charactherized by thrombocytosis and hyperplasia of megakaryocytes in the bone marrow. other cell lines are not involved.jak2v617fmutations has been identified in approximately half the patients with this disorder. we describe a 12-year-old boy with essential throbocythemia. the pa...

Journal: :iranian journal of blood and cancer 0
valizadeh n eishi oskuie a oni heris s

this is a picture presentation of myeloproliferative disorder developing to longitudinal melanonychia as a side effect of hydroxyurea. keywords: melanonychia, hydroxyurea, side effect.

Eishi Oskuie A, Oni Heris S, Valizadeh N,

This is a picture presentation of myeloproliferative disorder developing to longitudinal melanonychia as a side effect of hydroxyurea. Keywords: Melanonychia, hydroxyurea, side effect.

Journal: :Leukemia research 2012
C Michael Jones

KEY WORDS: Imatinib mesylate Polycythemia Vera Myeloproliferative disorder Myeloproliferative neoplasm Tyrosine kinase inhibitor Myelosuppressive therapy

2005
T. Miyashita S. Mizutani M. Asada J. Fujimoto T. Inaba T. Furukawa

Transient myeloproliferative disorder is a hematological condition observed during the neonatal period in patients with Down syndrome [1]. This disorder mimics congenital leukemia and the blast cells were often reported to show characteristics compatible with those of megakaryoblasts [2] or pluripotent stem cells [3]. Although this disorder usually resolves gradually without antileukemic treatm...

Journal: :Indian pediatrics 1996
S M Dhaded R Das P Kumar A Narang

Children with Down's syndrome are at an increased risk for development of several hematological disorders like acute leukemia, acute myelofibrosis of childhood and transient myeloproliferative disorder (TMD)(1). Transient myeloproliferative disorder is recognized shortly after birth or in neonatal period and is characterized by leukocytosis and thrombocytopenia, which resolves spontaneously in ...

Journal: :iranian red crescent medical journal 0
sangeetha vijay regional cancer centre, division of cancer research, medical college po, thiruvananthapuram-695 011, kerala, india geetha narayanan regional cancer centre, division of medical oncology, medical college po, thiruvananthapuram-695 011, kerala, india santhi sarojam regional cancer centre, division of cancer research, medical college po, thiruvananthapuram-695 011, kerala, india suresh kumar raveendran regional cancer centre, division of cancer research, medical college po, thiruvananthapuram-695 011, kerala, india sreedharan hariharan regional cancer centre, division of cancer research, medical college po, thiruvananthapuram-695 011, kerala, india; regional cancer centre, division of cancer research, medical college po, thiruvananthapuram-695 011, kerala, india. tel: +91-712522204, fax: +471-2447454

conclusions both the cases discussed in our study have inv(9) as the sole abnormality and are found to confer a relatively poor prognosis. case presentation we present the case of a chronic myeloid leukemia (cml) patient who showed intermittent relapse on treatment, with a rare appearance of clones with dual inversion (9) breakpoints [inv(9)(p22q34); inv(9)(p11q21)]. we also present the first r...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1988
J Haan J F Caekebeke F J van der Meer A R Wintzen

Two patients with cerebral venous thrombosis are described. In both patients laboratory findings suggested an underlying haematological disorder and bone marrow biopsy showed a myeloproliferative disorder. Both chronic cerebral venous thrombosis and early myeloproliferative disorders are difficult to diagnose. Their combined occurrence may be less rare than is frequently supposed.

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