Results 191 to 200 of about 87,925 (315)

Improved post‐transplant outcomes since 2000 for Ph‐positive acute lymphoblastic leukemia in first remission: A study from the EBMT Acute Leukemia Working Party

open access: yesHemaSphere, Volume 9, Issue 4, April 2025.
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

CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy [PDF]

open access: bronze, 2003
Animesh Pardanani   +12 more
openalex   +1 more source

Frequency and Characteristics of Gastrointestinal Diseases in Patients With Neurofibromatosis

open access: yesJGH Open, Volume 9, Issue 4, April 2025.
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

A network-based approach to overcome BCR::ABL1-independent resistance in chronic myeloid leukemia. [PDF]

open access: yesCell Commun Signal
Bica V   +15 more
europepmc   +1 more source

Efficacy of imatinib mesylate in the treatment of idiopathic hypereosinophilic syndrome [PDF]

open access: bronze, 2003
Jorge E. Cortés   +9 more
openalex   +1 more source

Lymphocytic Variant Hypereosinophilic Syndrome: Case Series From a Tertiary Referral Center in Canada

open access: yeseJHaem, Volume 6, Issue 2, April 2025.
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

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