Примери за използване на Myelofibrosis на Английски и техните преводи на Български
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Myelofibrosis(MF).
Multiple myeloma Myelofibrosis.
In myelofibrosis, Jakavi was investigated in two main studies involving 528 patients.
Does anything work for anaemia in myelofibrosis?
Myelofibrosis has been observed in the bone marrow of rats at all tested dose levels.
It can progress to myelofibrosis or AML.
Myelofibrosis is a disorder of the bone marrow, in which the marrow is replaced by scar tissue.
National Registry of Patients with Myelofibrosis.
The recommended starting dose in myelofibrosis is 15 mg twice daily or 20 mg twice daily.
An enlarged spleen also might be due to a bone marrow condition, such as myelofibrosis(MI-eh-lo-fi-BRO-sis).
In myelofibrosis, the recommended starting dose is up to 20 mg twice a day depending on the platelet count.
The disease may progress to myelofibrosis or AML.
In myelofibrosis, Jakavi was more effective than placebo and the best available treatment at reducing the size of the spleen.
When you stop taking Jakavi, the myelofibrosis symptoms may come back.
Myelofibrosis is a disease in which the bone marrow becomes very dense and rigid and produces abnormal, immature blood cells.
Anemia due to bone marrow diseases such as leukemia or myelofibrosis affect the bone marrow's ability to make blood cells.
In myelofibrosis and polycythaemia vera, there is too much JAK activity, leading to the abnormal production of blood cells.
Bone marrow aspirate and biospy:to rule out other causes of pancytopenia(i.e. neoplastic infiltration or significant myelofibrosis).
The recommended starting dose in myelofibrosis is 15 mg twice daily or 20 mg twice daily, depending on your blood cell count.
Jakavi is used to treat adult patients with an enlarged spleen orwith symptoms related to myelofibrosis, a rare form of blood cancer.
In these studies, myelofibrosis was not observed in animals after a 4-week post-treatment recovery period, indicating reversibility.
We found out more frequent JAK2V617F mutational burden in patients with primary myelofibrosis(PMF)(70%) compared to literature data.
In myelofibrosis the CHMP considered that the reduction in spleen size and symptoms seen in patients taking Jakavi is clinically important.
At the time of the withdrawal of application,the CHMP was of the provisional opinion that Enpaxiq could not have been approved for myelofibrosis.
The company presented data from a main study in 327 patients with myelofibrosis that looked at the number of patients whose spleen size reduced by at least 35% after 24 weeks of treatment.
Enpaxiq was designated an‘orphan medicine'(a medicine to be used in rare diseases)on 25 August 2010 for different types of myelofibrosis.
Diagnoses of primary and secondary myelofibrosis, in accordance with the current international standards in clinical hematology, were the inclusion criteria for registering.
Among the severe and terrible consequences of rickets are osteomalacia, osteoporosis,posture disorder, myelofibrosis, multiple caries of all teeth, anemia.
These included myelofibrosis and splenic hypertrophy as well as broadening of the ECG-QRS complex in dogs but no dysrhythmia and no effect on the QT interval were observed.
On 20 February 2017, CTI BioPharma officially notified the Committee for Medicinal Products for Human Use(CHMP) that it wishes to withdraw its application for a marketing authorisation for Enpaxiq, for treating patients with an enlarged spleen orother symptoms of myelofibrosis.