Placenta. 2025 Feb 20;162:51-58. doi: 10.1016/j.placenta.2025.02.011. Online ahead of print. ABSTRACT INTRODUCTION: The umbilical cord (UC) anatomically embodies the feto-placental bridge with a major role …
Acta Neuropathol Commun. 2025 Feb 27;13(1):43. doi: 10.1186/s40478-025-01945-w. ABSTRACT Diffuse hemispheric glioma H3 G34-mutant (DHG) has been identified as a distinct pediatric-type high-grade glioma, according …
BMC Pharmacol Toxicol. 2025 Feb 27;26(1):45. doi: 10.1186/s40360-025-00882-7. ABSTRACT BACKGROUND: Myelodysplastic Syndrome (MDS) is a devastating hematologic malignancy associated with advanced age. Diabetes Mellitus (DM) …
BMC Pharmacol Toxicol. 2025 Feb 27;26(1):47. doi: 10.1186/s40360-025-00874-7. ABSTRACT BACKGROUND: Linezolid (LZD) is used to treat infectious diseases caused by Gram-positive bacteria, but thrombocytopenia is …
Orphanet J Rare Dis. 2025 Feb 27;20(1):90. doi: 10.1186/s13023-024-03268-w. ABSTRACT BACKGROUND: Achondroplasia, a disease characterized by disproportionate short stature and increased morbidity, affects daily function …
Eur J Med Res. 2025 Feb 27;30(1):142. doi: 10.1186/s40001-025-02392-y. ABSTRACT BACKGROUND: Malnutrition is a significant concern in children with β-thalassemia, impacting their growth and overall …
Clin Epigenetics. 2025 Feb 27;17(1):38. doi: 10.1186/s13148-025-01847-7. ABSTRACT Currently, the non-invasive diagnostic methods for nasopharyngeal carcinoma (NPC) continue to grapple with the challenge of low …
Hered Cancer Clin Pract. 2025 Feb 27;23(1):9. doi: 10.1186/s13053-024-00303-6. ABSTRACT BACKGROUND: Germline genetic susceptibilities of rare cancers of the esophagus, stomach, small intestine, testis, (nonmedullary) …
Glob Health Res Policy. 2025 Feb 27;10(1):11. doi: 10.1186/s41256-024-00395-6. ABSTRACT BACKGROUND: Despite being included in the Millennium Development Goals (MDGs) and now the Sustainable Development …
Orphanet J Rare Dis. 2025 Feb 27;20(1):89. doi: 10.1186/s13023-024-03314-7. ABSTRACT BACKGROUND: Disorder-related variants in the STXBP1 gene are increasingly detected in children with severe developmental …
