Ara
Toplam kayıt 2, listelenen: 1-2
MPL W515L/K mutations in chronic myeloproliferative neoplasms
(Galenos Yayınevi, 2013)
The MPL gene encodes the thrombopoietin receptor. Recently MPL mutations (MPL W515L or MPL W515K) were described in patients with essential thrombocythemia (ET) and primary (idiopathic) myelofibrosis (PMF). The prevalence ...
Neurologic involvement in atypical hemolytic uremic syndrome and successful treatment with eculizumab
(Springer Verlag, 2013)
Background
Atypical hemolytic uremic syndrome (aHUS) is associated with defective regulation of the complement pathway. Neurological involvement is the most common extrarenal complication and represents a major cause of ...