Results 121 to 130 of about 37,157 (250)
American Journal of Hematology, Volume 101, Issue 10, Page 2654-2658, October 2026.
Alma Al Sibaaie +12 more
wiley +1 more source
ABSTRACT Hydroxyurea (HU) is the most widely prescribed disease‐modifying treatment in sickle cell disease (SCD), though treatment responses vary due to metabolism and adherence. We examined HU blood levels and treatment response in patients with homozygous sickle cell disease (HbSS).
Sigrid van der Veen +26 more
wiley +1 more source
American Journal of Hematology, Volume 101, Issue 10, Page 2666-2671, October 2026.
Kenneth I. Ataga +8 more
wiley +1 more source
The methanolic extract of Cinnamomum verum exhibited antibacterial and antibiofilm activities, enhanced the efficacy of conventional antibiotics against multidrug‐resistant bacteria, and showed favorable interactions with key bacterial targets in molecular docking analyses, supporting its potential as a natural antimicrobial adjuvant for combating ...
Hayet Edziri +11 more
wiley +1 more source
Device-to-Device (D2D) communication has emerged as a pivotal technology for fifth-generation (5G) and sixth-generation (6G) wireless networks, enabling direct communication between proximate devices while bypassing the base station.
Iacovos I. Ioannou +2 more
doaj +1 more source
ABSTRACT A 67‐year‐old man with decades of untreated sickle cell disease developed septic shock with multiorgan failure, splenic infarction, and marrow fibrosis; his genotype could not be confirmed. He recovered with intensive supportive care, with hydroxyurea initiated for long‐term disease modification, illustrating catastrophic infection‐triggered ...
Sara Shahidi, Gisha Mohan
wiley +1 more source
ABSTRACT Sickle cell leg ulcers (SCLUs) are a chronic and debilitating complication of sickle cell disease (SCD), often associated with severe pain, impaired mobility, delayed healing, and recurrence. Their management remains challenging because ulcer formation and persistence are driven by multiple overlapping mechanisms, including hemolysis ...
Jamil Wafi +2 more
wiley +1 more source
ABSTRACT Sickle cell disease (SCD) with hemoglobin‐ (Hb‐) SC genotype is often considered a milder SCD variant, yet life‐threatening complications can occur. A 26‐year‐old man with HbSC disease presented with an infection triggered vaso‐occlusive crisis (VOC), acute chest syndrome (ACS), severe thrombocytopenia, Coombs‐negative hemolysis with ...
Benjamin Vieten +9 more
wiley +1 more source
Trombosis de grandes vasos: un problema emergente [PDF]
Paralelo al inicio de la hemodiálisis como terapia renal sustitutiva surge la pregunta de cuál es el mejor acceso vascular. Clásicamente se ha considerado que el mejor acceso es la fístula arterio-venosa (FAVI), ya que en comparación con el catéter ...
García Parejo, Cristina +3 more
core +1 more source

