Results 201 to 210 of about 67,237 (303)
Seroprevalence and Associated Risk Factors of Foot-and-Mouth Disease in Livestock in Ethiopia: Findings From a National Surveillance (2016-2023). [PDF]
Gizaw D +8 more
europepmc +1 more source
Abstract Pregnancy‐ and lactation‐associated osteoporosis (PLO) is a syndrome characterized by fragility fractures (most commonly vertebral, often multiple) occurring in late pregnancy or the early postpartum period. This position statement summarizes the current knowledge of PLO, and the recommended procedure for assessment, diagnosis and treatment ...
Peyman Hadji +20 more
wiley +1 more source
Social, economic, and transboundary importance of foot and mouth disease quarantines in East Africa. [PDF]
Railey AF, Kerfua SD, Marsh TL.
europepmc +1 more source
Gait analysis can provide valuable information for identifying changes in movement associated with neurological disorders, thus serving as an important support tool in several areas, including healthcare and rehabilitation. In this study, zinc oxide/polydimethylsiloxane (ZnO/PDMS)‐coated carbon fiber yarns were developed and evaluated as pressure ...
Maria Morais +10 more
wiley +1 more source
Genetic Variation and Evolutionary Characteristics of Coxsackievirus B1: F3 Subtype Associated With Hand, Foot and Mouth Disease in China. [PDF]
Lin J +14 more
europepmc +1 more source
Following traumatic brain injury, indole‐3‐propionic acid (IPA) directly targets the aryl hydrocarbon receptor on astrocytes in the peri‐lesional cortex; this suppresses interferon regulatory factor 1‐driven transcription of the E3 ubiquitin ligase RFFL (ring finger and FYVE‐like domain containing E3 ubiquitin protein ligase).
Ziwen Zhang +22 more
wiley +1 more source
Isolation and molecular characterization of foot-and-mouth disease viruses from small ruminants in Nigeria. [PDF]
Ehizibolo DO +14 more
europepmc +1 more source
Distal 1q43q44 deletions lead to a consistent neurodevelopmental phenotype characterized by microcephaly, corpus callosum abnormalities, and developmental delay. Despite differences in genomic architecture, overlapping deletions affecting dosage‐sensitive genes such as AKT3, HNRNPU, and ZBTB18 define the core phenotype.
Ma. Guadalupe Domínguez‐Quezada +6 more
wiley +1 more source

