Results 231 to 240 of about 43,706 (302)

Leukemic Regression After G‐CSF Withdrawal in Severe Congenital Neutropenia

open access: yes
eJHaem, Volume 7, Issue 1, February 2026.
Agnese Roveta   +8 more
wiley   +1 more source

Clinical Utility of Frailty Scoring in Elderly Acute Myeloid Leukemia Patients Treated With Venetoclax and Hypomethylating Agents

open access: yesEuropean Journal of Haematology, Volume 116, Issue 2, Page 160-168, February 2026.
ABSTRACT Acute myeloid leukemia (AML) in elderly patients presents a major therapeutic challenge, as many are deemed unfit for intensive chemotherapy due to age, comorbidities, or frailty. Venetoclax in combination with hypomethylating agents (HMA) has emerged as a standard‐of‐care for this population, yet outcomes remain heterogeneous and predictive ...
Ernesto Vigna   +11 more
wiley   +1 more source

ICSH Recommendations for Monocyte Cell Lineage Morphologic Identification, Nomenclature Harmonization, and Utilization as a Biomarker

open access: yesInternational Journal of Laboratory Hematology, Volume 48, Issue 1, Page 12-25, February 2026.
ABSTRACT Monocytes are key components of the Mononuclear Phagocyte System, crucial in immune defense, inflammation, and tissue repair. Accurate identification and classification of monocyte lineage cells are essential for diagnosing both reactive and clonal hematologic disorders.
Gina Zini   +10 more
wiley   +1 more source

Comprehensive Clinical, Diagnostic, and In Silico Assessment of a Novel 1p36.33p36.32 Copy Number Variant

open access: yesJournal of Cellular and Molecular Medicine, Volume 30, Issue 4, February 2026.
ABSTRACT Clinical manifestations of 1p36.33 duplications vary depending on duplication size. This region is prone to copy number variants associated with diverse phenotypes. We report a novel 1p36.33p36.32 duplication in a patient with developmental delay and facial dysmorphism. The causative duplication was detected by whole‐genome Oligo‐array CGH and
Atieh Eslahi   +11 more
wiley   +1 more source

Balancing benefit and burden: treatment intensification in paediatric KMT2A rearrangements acute myeloid leukaemia. [PDF]

open access: yesActa Oncol
Fayez H   +9 more
europepmc   +1 more source

Massive Genomic and Transcriptomic Changes Within a Young Inversion Polymorphism in the Absence of Degeneration

open access: yesMolecular Ecology, Volume 35, Issue 4, February 2026.
ABSTRACT Chromosomal inversion polymorphisms have been linked to the evolution of phenotypic variation, environmental adaptation, and speciation. The genome of the white‐throated sparrow (Zonotrichia albicollis) contains two exceptionally large chromosomal polymorphisms.
Nicole M. Baran   +3 more
wiley   +1 more source

Home - About - Disclaimer - Privacy