Results 181 to 190 of about 29,542 (277)

Common Hematologic Emergencies—Acute Promyelocytic Leukemia and Microangiopathic Hemolytic Anemias—A Pivotal Role of Clinical Laboratory

International Journal of Laboratory Hematology, Volume 48, Issue 3, Page 521-530, June 2026.
ABSTRACT Hematologic emergencies are urgent health conditions which result in significant mortality and morbidity unless timely therapeutic measures are taken. Therapeutic success depends on their timely and accurate recognition by hematology laboratory services.
Ganna Shestakova, Nicolas Ulrich Edgar, Anton V. Rets   +2 more
wiley   +1 more source

Persistent proteinuria among a cohort of Nigerian children with sickle cell anaemia. [PDF]

PLoS One
Adeoti-Lawani AE, Ezeh GO, Oyenusi EE, Esezobor CI.   +3 more
europepmc   +1 more source

Addressing racial disparities in representation across blood, stem cell and organ and tissue donor pools

Vox Sanguinis, Volume 121, Issue 6, Page 710-721, June 2026.
Abstract Background and Objectives Adequate representation of donors from diverse ancestral populations in blood, stem cell and organ transplantation is critical to ensuring equitable access to these lifesaving therapies. Because of population‐level differences in genetic markers, patients from racialized groups may have unique transfusion and ...
Bonnie Lu, Sylvia Okonofua, Farnaz Farahbakhsh, Rupal Hatkar, Lauren Sano, Margarita Conway, Marie‐Claire Kapesa, Manuel Escoto, Murdoch Leeies, Warren B. Fingrut   +9 more
wiley   +1 more source

Hypoxic‐hypocapnic red blood cells in PAGGSM additive solution before and after gamma irradiation show improved metabolism

Vox Sanguinis, Volume 121, Issue 6, Page 801-808, June 2026.
Abstract Background and Objectives Hypoxic/hypocapnic (HH) treatment and storage conditions have been shown to reduce oxidative stress and improve red blood cell (RBC) quality. This study aimed to validate a good manufacturing practice HH RBC product for obtaining the licence for routine use in patients, by comparison with normoxic RBCs both without ...
Soroth Chey, Jacqueline Maier, Samuel Sowemimo‐Coker, Reinhard Henschler   +3 more
wiley   +1 more source

Serum ferritin in Yemeni patients with sickle cell anemia: Association with sociodemographic factors and hematological profiles. [PDF]

PLoS One
Al-Shami A, Al-Maktari LAS, Qasem L, Aldhorae K, Al-Khaship S.   +4 more
europepmc   +1 more source

Neuregulin‐1 Mitigates Kidney Injury in Humanized Sickle Cell Mice

The FASEB Journal, Volume 40, Issue 10, 31 May 2026.
Compared with untreated sickle cell (HbSS) mice, neuregulin‐1 (NRG‐1) treatment reduced plasma heme, lactate dehydrogenase, and pro‐inflammatory cytokines while increasing the proportion of circulating F‐cells. NRG‐1 improved urinary biomarkers of kidney health, decreasing cystatin C and NGAL levels and increased renal repair markers clusterin and ...
William K. Agbozo, Wesley Solomon, Isaac Joe Erskine, Cecilia E. Lekpor, Oguljahan Babayewa, Alaijah Bashi, Adriana Harbuzariu, Aqua Asberry, Driss Adel, Samuel Adjei, Lily Paemka, Solomon F. Ofori‐Acquah, Jonathan K. Stiles   +12 more
wiley   +1 more source

High-performance liquid chromatography screening reveals HbS/β+-thalassemia double heterozygosity as a pediatric muscular dystrophy mimic. [PDF]

Lab Med
López-Medina C, Portell-Rigo IM, González-Iribarren V, González-Oller C, Sánchez-Crespo A, Molina-Arrebola MA.   +5 more
europepmc   +1 more source

Evaluation of surgical evacuation of the uterus for abortion and management of miscarriage in patients with sickle cell disease: A multicentre UK study

British Journal of Haematology, Volume 208, Issue 6, Page 2307-2310, June 2026.
Sonia Wolf, Natasha Lewis, Funmi Oyesanya, Karlene Birthwright, Tracey Masters, Andriana Andreeva   +5 more
wiley   +1 more source

Oral Radiographic Changes in Severe Sickle Cell Anemia Patients: A Retrospective Comparative Study. [PDF]

Clin Cosmet Investig Dent
AlKhodier H, Bin Saleh F, AlRumi A, AlOjaym T.   +3 more
europepmc   +1 more source

Differential complement activation by alloantibodies in sickle cell hyperhaemolysis syndrome may influence disease course

British Journal of Haematology, Volume 208, Issue 6, Page 2311-2314, June 2026.
Mamie M. Thant, Jahnavi Gollamudi, Stefanie W. Benoit, Satheesh Chonat, Jose A. Cancelas   +4 more
wiley   +1 more source