Abstract Allogeneic hematopoietic cell transplantation (allo‐HCT) remains a curative treatment for patients with Philadelphia chromosome‐positive acute lymphoblastic leukemia (Ph+ ALL) in their first complete remission (CR1). Recent results using the combination of blinatumomab and second‐ or third‐generation tyrosine kinase inhibitors have challenged ...
Ali Bazarbachi+18 more
wiley +1 more source
New onset diabetes manifesting as diabetic ketoacidosis in a patient with chronic myelogenous leukemia treated with imatinib. [PDF]
Salimova D+4 more
europepmc +1 more source
CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy [PDF]
Animesh Pardanani+12 more
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Frequency and Characteristics of Gastrointestinal Diseases in Patients With Neurofibromatosis
ABSTRACT Background and Aim Patients with neurofibromatosis (NF) frequently experience gastrointestinal symptoms, but the specific characteristics of these lesions are not well understood. Methods To investigate the prevalence and nature of gastrointestinal diseases in this population, we analyzed the gastrointestinal lesions identified through ...
Manami Honda+7 more
wiley +1 more source
Further Insight Found into Molecular Basis for Imatinib Resistance in CML
Peggy Peck
openalex +1 more source
BCR/ABL kinase inhibition by imatinib mesylate enhances MAP kinase activity in chronic myelogenous leukemia CD34+ cells [PDF]
Su Chu+3 more
openalex +1 more source
A network-based approach to overcome BCR::ABL1-independent resistance in chronic myeloid leukemia. [PDF]
Bica V+15 more
europepmc +1 more source
Imatinib Superior to Standard Therapy in Newly Diagnosed CML
Lilian Delmonte
openalex +1 more source
Efficacy of imatinib mesylate in the treatment of idiopathic hypereosinophilic syndrome [PDF]
Jorge E. Cortés+9 more
openalex +1 more source
ABSTRACT Background Lymphocytic variant hypereosinophilic syndrome (L‐HES) is a rare disorder characterized by persistent eosinophilia driven by aberrant T‐cell populations. Diagnosis remains challenging due to the lack of standardized diagnostic criteria.
Xiu Qing Wang+6 more
wiley +1 more source