EJNMMI Res. 2025 Sep 26;15(1):120. doi: 10.1186/s13550-025-01313-8. ABSTRACT BACKGROUND: We aimed to estimate 82Rb paediatric dosimetry based on adult biokinetic and prospectively acquired paediatric biokinetic …
J Pers Med. 2025 Sep 1;15(9):406. doi: 10.3390/jpm15090406. ABSTRACT Background: Autoimmune rheumatic diseases, including systemic lupus erythematosus (SLE), antiphospholipid syndrome (APS), Sjögren’s syndrome, systemic sclerosis …
Trop Med Infect Dis. 2025 Sep 18;10(9):270. doi: 10.3390/tropicalmed10090270. ABSTRACT Operational research (OR) published in 2023 revealed low utilisation and suboptimal quality of blood culture …
Cells. 2025 Sep 16;14(18):1452. doi: 10.3390/cells14181452. ABSTRACT Sepsis-induced cardiomyopathy is a life-threatening complication lacking targeted therapies. While empagliflozin (Empa), a sodium-glucose cotransporter 2 (SGLT2) inhibitor, …
Metabolites. 2025 Sep 22;15(9):634. doi: 10.3390/metabo15090634. ABSTRACT Background/Objectives: Dutch newborn screening is an important public health program designed to detect conditions early in life, enabling …
Cells. 2025 Sep 13;14(18):1434. doi: 10.3390/cells14181434. ABSTRACT Neonatal rodent cardiomyocytes (CMs) are a mainstay of in vitro cardiac research, yet their immature phenotype limits the …
Toxicol Sci. 2025 Sep 26:kfaf132. doi: 10.1093/toxsci/kfaf132. Online ahead of print. ABSTRACT There is a paucity of in vitro models to study the male reproductive …
Biosensors (Basel). 2025 Sep 3;15(9):577. doi: 10.3390/bios15090577. ABSTRACT Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common enzymopathy with significant clinical implications, particularly in malaria-endemic regions and …
O G Open. 2024 Dec 5;1(4):50. doi: 10.1097/og9.0000000000000050. eCollection 2024 Dec. ABSTRACT OBJECTIVE: To estimate the optimal timing of delivery among pregnant patients with chronic …
O G Open. 2024 Nov 7;1(4):43. doi: 10.1097/og9.0000000000000043. eCollection 2024 Dec. ABSTRACT BACKGROUND: Generalized arterial calcification of infancy is a rare genetic disorder that was …
