Results 241 to 250 of about 184,260 (294)

<i>CHEK2</i> germline variants in B-cell precursor acute lymphoblastic leukemia: findings in Mexican pediatric patients. [PDF]

open access: yesFront Oncol
Martínez Anaya D   +8 more
europepmc   +1 more source

Pharmacological inhibition of sclerostin protects bone from B‐cell acute lymphoblastic leukemia‐mediated destruction

open access: yes
HemaSphere, Volume 10, Issue 4, April 2026.
Vincent Kuek   +8 more
wiley   +1 more source

Acute Lymphoblastic Leukemia

Hematology, 2002
AbstractThis is a comprehensive overview on the most recent developments in diagnosis and treatment of acute lymphoblastic leukemia (ALL).Dr. Dieter Hoelzer and colleagues give an overview of current chemotherapy approaches, prognostic factors, risk stratification, and new treatment options such as tyrosine kinase inhibitors and monoclonal antibodies ...
Dieter, Hoelzer   +7 more
  +7 more sources

Acute Lymphoblastic Leukemia

2007
Acute lymphoblastic leukemia (ALL) comprises a heterogeneous group of disorders which originate from various important genetic lesions in B and T progenitor cells, including mutations that lead to stage-specific developmental arrest and those that impart the capacity for unlimited self-renewal, resulting in clonal expansion of immature progenitor cells
Biondi A., Scrideli C. A., Cazzaniga G.
  +5 more sources

Acute Lymphoblastic Leukemia

Clinics in Laboratory Medicine, 2000
Over the last two decades, great strides have been made in the treatment of acute lymphoblastic leukemia (ALL). This progress has been paralleled by advances in diagnosis. In addition to morphology and cytochemistry, the diagnostic and prognostic importance of immunophenotypic and genetic features is becoming increasingly apparent. This article reviews
D C, Farhi, N S, Rosenthal
openaire   +2 more sources

Acute Lymphoblastic Leukemia

Pediatric Clinics of North America, 1997
Advances in the molecular and immunologic characterization of leukemic cells have greatly aided the diagnosis and risk assignment of ALL, as well as the monitoring of bone marrow samples for minimal residual disease. Currently, 75% of childhood cases have biologically and therapeutically relevant genetic abnormalities.
openaire   +3 more sources

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