Results 231 to 240 of about 78,018 (293)

Immunophenotypic abnormality quantification refines multiparameter flow cytometry-based measurable residual disease testing in adults allografted for acute myeloid leukemia in morphologic remission. [PDF]

Hemasphere
Le CM, Chen X, Kodaira S, Othus M, Gang M, Davis C, Basom RS, Cherian S, Walter RB.   +8 more
europepmc   +1 more source

Standardizing the Clinical Approach to Cancer Therapy‐Related Cardiac Dysfunction: Applying Cardio‐Oncology Guidelines as a Practical Tool for Hematology and Oncology Providers

Cancer Medicine, Volume 15, Issue 4, April 2026.
ABSTRACT Introduction and Methods Cancer therapy–related cardiac dysfunction (CTRCD) is a well established and potentially life‐threatening complication of contemporary oncologic treatment. Although comprehensive cardio‐oncology guidelines have been developed, their integration into routine hematology and oncology practice remains inconsistent.
Abdelrahman Ali, Suparna C. Clasen, Anne Blaes, Stephen Casselli, Anita Deswal, Susan Halli Demeter, Gregory Durm, Anecita Fadol, Alessandra Ferrajoli, Michael G. Fradley, Joerg Herrmann, Borja Ibanez, Sue Koob, Bogda Koczwara, Kasey J. Leger, Jennifer E. Liu, Teresa López‐Fernández, Alexander R. Lyon, N. G. Choon Ta, John Teerlink, Eric H. Yang, Susan Dent, Daniel Lenihan   +22 more
wiley   +1 more source

Clinical factors associated with venous thromboembolism in multiple myeloma patients treated with daratumumab. [PDF]

Discov Med (Singap)
Subramanian NG, Aung FM, Hunzeker ZE, Patel KK, Lee HC, Jin S, Young E, Bassett RL, Rojas Hernandez CM.   +8 more
europepmc   +1 more source

Brachymetatarsia as an Early Clue to Turner Syndrome

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Congenital anomalies of the extremities, particularly bilateral toe or finger malformations, may provide an early and valuable clue to an underlying genetic disorder and should prompt further diagnostic evaluation. Brachymetatarsia is a rare associated finding that may raise suspicion for Turner syndrome, particularly when diagnosis is delayed
Hounaida Mahfoud, Zaki Elhanchi
wiley   +1 more source

P140: A rare phenomenon: Double trisomy rescue detected during clinical SNP microarray testing*

Genetics in Medicine Open
Andrea Penton, Peter Papenhausen, Stuart Schwartz, Anh Vu, Gloria Haskell   +4 more
doaj   +1 more source

Clinicopathological Spectrum of Acute Myeloid Leukemia and Treatment Outcomes in Kashmiri Population: A Prospective Study.

J Pharm Bioallied Sci
Khan AA, Geelani SA, Rathod SG, Roshan R, Chozakade A, Bhat JR, Hussain S, Atta A.   +7 more
europepmc   +1 more source

A left basal ganglia lesion in a 57-year-old patient. [PDF]

Brain Pathol
Atiya S, Sonani A, Eickoff J, Vizcaino MA.   +3 more
europepmc   +1 more source

Polytypic and polymorphic cytogenetic variations in the widespread anuran Physalaemus cuvieri (Anura, Leiuperidae) with emphasis on nucleolar organizing regions

, 2009
Yrsd Quindere, L.H. Lourenço, GV Andrade, Cristian Tomatis, Diego Baldo, SM Recco-Pimentel   +5 more
openalex   +1 more source

Down Syndrome due to de Novo Robertsonian Translocation Rob(21;21) in Mali

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Down syndrome (DS) is the most common chromosomal disorder among live births, most frequently resulting from free trisomy 21. Robertsonian translocations, which arise from the fusion of acrocentric chromosomes, represent a rare but clinically significant mechanism underlying DS.
Christine Ongoiba, Oumar Samassekou, Oumou Traoré, Cheick O. Sidibé, Modibo K. Goita, Guida Landouré, Mahamadou Traoré   +6 more
wiley   +1 more source

Outcomes of therapy-related non-core binding factor acute myeloid leukemia with venetoclax-based therapies. [PDF]

Hemasphere
Senapati J, Croden J, Garcia-Manero G, Takahashi K, Daver NG, Kadia TM, Borthakur G, Short NJ, Jabbour E, Haddad F, Marvin-Peek J, Abbas HA, Bose P, Tang G, Loghavi S, Shpall EJ, Ramdial J, Popat UR, Champlin RE, Ravandi F, Kantarjian HM, Dinardo CD.   +21 more
europepmc   +1 more source