Mostrando 1,541 - 1,560 Resultados de 3,184 Para Buscar '"Oi!"', tiempo de consulta: 0.31s Limitar resultados
  1. 1541
    “…Orthostatic intolerance (OI) is frequently reported in young women with generalized hypermobility spectrum disorder (G‐HSD) and hypermobile EDS (hEDS). …”
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  2. 1542
    “…OI-exo-delivered hierarchical mesoporous bioactive glass (MBG) scaffold effectively promote in vivo bone formation in aging rat cranial defect model. …”
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  3. 1543
    “…This novel pilot study examined differences in cerebral hemodynamics, as measured using functional near-infrared spectroscopy (fNIRS), and its association with diffusion tensor imaging (DTI) metrics in children with mTBI or mild orthopedic injury (OI) to address these gaps. Children 8.00–16.99 years of age with mTBI (n = 9) or OI (n = 6) were recruited in a pediatric emergency department, where acute injury characteristics were assessed. …”
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  4. 1544
    por Lang, Erica, Semon, Julie A.
    Publicado 2023
    “…Osteogenesis imperfecta (OI) is a disease caused by mutations in different genes resulting in mild, severe, or lethal forms. …”
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  5. 1545
    “…Herein, we fused induced pluripotent stem cell-derived endothelial cell (iEC) membrane together with M1 type macrophage membrane to construct a hybrid membrane (iEC-M) camouflaged 4OI nanovesicles (4OI@iEC-M). Furthermore, bioinspired nanovesicles 4OI@iEC-M are incorporated into the injectable, multifunctional gelatin methacryloyl hydrogels for diabetic wound repair and regeneration. …”
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  6. 1546
    “…Early embryonic loss was 6.7% points lower for cows inseminated at a stronger OI (OI = 3) compared to at a weaker OI (OI = 2, P = 0.006). …”
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  7. 1547
  8. 1548
    “…The silence of Nrf2 abolished the inhibition of ferroptosis from 4-OI in THP-1 cells. Additionally, the protection of 4-OI for ALI was abolished in Nrf2-knockout mice. …”
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  9. 1549
  10. 1550
  11. 1551
    “…Background and Objectives: Odontogenic infections (OI) represent a frequent cause of dental and maxillo-facial interventions, mostly due to late presentations or misdiagnosed complications. …”
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  12. 1552
  13. 1553
  14. 1554
    “…Osteogenesis imperfecta (OI) is generally caused by a dominant mutation in Collagen I, encoded by the genes COL1A1 and COL1A2. …”
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  15. 1555
    por Lavanya, R, Deepika, K, Patil, Madhuri
    Publicado 2009
    “…Both heterotopic pregnancy and spontaneous twinning are frequent after OI, this combination although extremely rare must be kept in mind. …”
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  16. 1556
    “…Osteogenesis imperfecta (OI) is the most common bone genetic disorder and it is characterized by bone brittleness and various degrees of growth disorder. …”
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  17. 1557
    “…One monoester ligand in Ti(2)(OiPr)(6)(μ(2)-OOC-C(6)H(4)-COOiPr)(η(1)-OOC-C(6)H(4)-COOiPr)(iPrOH) is bridging and the other is η(1)-coordinated. …”
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  18. 1558
    “…Osteogenesis imperfecta (OI) is a heterogeneous disorder of connective tissue that manifests mainly as skeletal deformity and bone fragility. …”
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  19. 1559
    por Hong, Deok Gi, Yoo, Doo Han
    Publicado 2017
    “…[Results] There were significant differences in items in the SFT, except for the respiratory item, between the OI group and the NOI group. There were significant differences in all items on the SWAL-QOL, except for the sleep item, between the OI group and the NOI group. …”
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  20. 1560
    “…Osteogenesis imperfecta (OI) is a rare inherited connective tissue disorder caused by mutation of collagen which results in a wide spectrum of clinical manifestations including long bone fragility fractures and deformities. …”
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