Results 181 to 190 of about 204,284 (266)

Vitamin D Deficiency and Its Hematological Correlates in Patients with Sickle Cell Disease at a Ugandan Clinic. [PDF]

J Blood Med
Salamu G, John EA, Wagubi R, Muwanguzi E, Bagenda CN, Okongo B.   +5 more
europepmc   +1 more source

Society for Maternal‐Fetal Medicine Special Statement: Checklists for persons with sickle cell disease in pregnancy

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract This article presents checklists designed to guide clinicians in the comprehensive management of pregnant individuals with sickle cell disease, including prepregnancy, antepartum, delivery, and postpartum care, as well as the specific management of vaso‐occlusive crises.
Society for Maternal‐Fetal Medicine (SMFM), Nicolina Smith, Rebecca F. Hamm, Jessica Peterson, Alexandra DeRusso Forrest, Nicole A. Smith, Jourdan E. Triebwasser, SMFM Patient Safety and Quality Committee   +7 more
wiley   +1 more source

Predicting Medication Adherence in Sickle Cell Disease and Thalassemia in Oman: The Role of Beliefs and Fatigue. [PDF]

Patient Prefer Adherence
Alshukaili WI, Al-Noumani H, Al Salmi N.
europepmc   +1 more source

Spirometry Patterns in Adult Sickle Cell Disease: A Retrospective Observational Study. [PDF]

Saudi J Med Med Sci
Almusally RM, Alghamdi R, Almubarak M, Ibrahim M, Alyousif H, Alelq Z, Alwaheed A, Alsultan O, Alsaeed A, Qutub H, Wert Y, Aljazeeri J.   +11 more
europepmc   +1 more source

Navigating Classical and Nonclassical Realms of Nucleation and Crystallization

Small, Volume 22, Issue 50, 7 September 2026.
Classical nucleation and growth theories have long been foundational, yet recent nonclassical concepts have challenged and refined our understanding of solid‐state genesis. This paradigm shift introduced new, often ambiguous vocabulary. Here, we clarify key concepts, correct common misconceptions, and provide a terminological field guide across systems,
Stephan E. Wolf, Peter G. Vekilov
wiley   +1 more source

Hematological Correlates of Hemoglobinopathies in Women of Reproductive Age With Anemia: A High-Performance Liquid Chromatography (HPLC)-Based Cross-Sectional Study. [PDF]

Cureus
Marandi S, Paswan MK, Jamaiyar A, Tirkey D, Mahto SK.   +4 more
europepmc   +1 more source

Sickle cell disease and fetal hemoglobin

Saudi Journal of Medicine and Medical Sciences, 2018
openaire   +3 more sources

The Haematological and Biochemical Responses of Goat Bucks to Range Grazing and Indoor Concentrate‐Based Feeding Systems

Veterinary Medicine and Science, Volume 12, Issue 5, September 2026.
ABSTRACT Background Range grazing remains the principal feed resource for goats in smallholder production systems, particularly in regions where range grazing and intensive concentrate‐based systems coexist. However, expanding cropland has reduced the availability of grazing lands and shifted production toward concentrate‐based feeding systems ...
Selamu Abraham, Yisehak Kechero, Jane Wamatu   +2 more
wiley   +1 more source

Distribution of Hemoglobin Variants: A Retrospective Study Based on Hemoglobin Electrophoresis Results From a University Hospital in Madagascar. [PDF]

Cureus
Fenomanana J, Rakotonjafiniarivo FH, Rasolozakandrainibe F, Niry Manantsoa S, Malalanirina AD, Ranaivosoa MK, Rakoto Alson AO.   +6 more
europepmc   +1 more source

Hydroxyurea (hydroxycarbamide) use in adults with haemoglobin SC disease: A real‐world study in Quebec

British Journal of Haematology, Volume 209, Issue 3, Page 1291-1300, September 2026.
Summary Haemoglobin SC (HbSC) disease is the second most prevalent form of sickle cell disease, but evidence for hydroxyurea (hydroxycarbamide; HU) to prevent pain episodes was limited until the prospective identification of variables as outcomes for treatment (PIVOT) trial.
Alice Girard, Laurianne Charette, Mélissa Haouchine, Laurence Bozec, Mohamed Zakaria Bachir Bouyadjera, Mariane Poitras, Vincent‐Thierry Taillefer, Chloé Trudeau, Yves Pastore, Nathalie Letarte, Stéphanie Forté   +10 more
wiley   +1 more source