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  1. 1221
    “…OBJECTIVE: Osteogenesis imperfecta (OI) is a rare inherited skeletal disease, characterized by bone fragility and low bone density. …”
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    Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta
  2. 1222
    “…Osteogenesis imperfecta (OI) is a family of genetic disorders associated with bone loss and fragility. …”
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    Online Artículo Texto
    Identification of a novel COL1A1 frameshift mutation, c.700delG, in a Chinese osteogenesis imperfecta family
  3. 1223
    “…Osteogenesis imperfecta (OI) is a genetic disorder causing skeletal fragility, multiple fractures, and other extraskeletal manifestations. …”
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    Online Artículo Texto
    A moderate form of osteogenesis imperfecta caused by compound heterozygous LEPRE1 mutations
  4. 1224
    “…The majority of patients with osteogenesis imperfecta (OI) have mutations in the COL1A1 or COL1A2 gene, which has consequences for the composition of the bone matrix and bone architecture. …”
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    Online Artículo Texto
    Current concepts in osteogenesis imperfecta: bone structure, biomechanics and medical management
  5. 1225
    “…Commonly, blood pressure (BP) and heart rate (HR) are monitored to observe for OI symptoms, but are indirect measurements of cerebral perfusion and can lead to inaccurate HUT evaluation. …”
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    Cerebral Perfusion Monitoring Using Near-Infrared Spectroscopy During Head-Up Tilt Table Test in Patients With Orthostatic Intolerance
  6. 1226
    “…In cluster 2, we found significant associations between image OI and FMA, AOU, and QOM. When AOU and QOM were mediated between image OI and FMA, we observed no significant direct association between image OI and FMA, and a significant indirect effect of AOU and QOM. …”
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    Motor‐imagery ability and function of hemiplegic upper limb in stroke patients
  7. 1227
    “…Osteogenesis Imperfecta (OI) is a heterogeneous genetic disorder characterized by bone fragility and fracture. …”
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    Osteogenesis imperfecta in Brazilian patients
  8. 1228
    “…BACKGROUND: Evidence suggests that olfactory impairment (OI) may be a degenerative neurologic complication of diabetes; however, the association is not yet well established. …”
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    The association between diabetes and olfactory impairment in adults: A systematic review and meta‐analysis
  9. 1229
    “…Glycolytic flux analysis by U(13)C glucose tracing provides evidence that 4-OI blocks glycolytic flux at GAPDH. 4-OI thereby downregulates aerobic glycolysis in activated macrophages, which is required for its anti-inflammatory effects. …”
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    4-Octyl itaconate inhibits aerobic glycolysis by targeting GAPDH to exert anti-inflammatory effects
  10. 1230
    “…Opportunistic infections (OIs) and advanced HIV disease (AHD) contribute to HIV-related mortality. …”
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    A Rapid Screening Program for Histoplasmosis, Tuberculosis, and Cryptococcosis Reduces Mortality in HIV Patients from Guatemala
  11. 1231
    “…The pathogenic variant, commonly ascribed to OI, as well as the benign variant, has been inherited from the individual's mother, who presented only mild signs of OI and the diagnosis of OI was confirmed only after molecular testing. …”
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    COL1-Related Disorders: Case Report and Review of Overlapping Syndromes
  12. 1232
    “…Here, we show the effect of the cell-permeable itaconate derivative 4-octyl itaconate (OI) on OA. OI attenuates the chondrocyte apoptosis induced by interleukin 1β (IL-1β) in vitro, indicating that OI protect chondrocytes against apoptosis. …”
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    Four-octyl itaconate improves osteoarthritis by enhancing autophagy in chondrocytes via PI3K/AKT/mTOR signalling pathway inhibition
  13. 1233
    “…Chronic rhinosinusitis with nasal polyps (CRSwNP) is a chronic type 2 inflammatory disease characterized by olfactory impairment (OI) as one of the most troublesome symptoms. Currently, biologics represent a new option in the treatment of uncontrolled type 2 CRSwNP. …”
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    Olfaction Recovery following Dupilumab Is Independent of Nasal Polyp Reduction in CRSwNP
  14. 1234
    “…Results: OI showed good dynamic range in the low-SUVR window. …”
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    The Overlap Index as a Means of Evaluating Early Tau PET Signal Reliability
  15. 1235
    “…In this work, three additives BiOX (BiOI, BiOBr, and BiOF) for Al-H(2)O reaction have been synthesized using chemical methods. …”
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    Improved Hydrogen Generation of Al-H(2)O Reaction by BiOX (X = Halogen) and Influence Rule
  16. 1236
    “…Osteogenesis imperfecta (OI) is a rare genetic disorder. Due to considerable phenotypic variability, a classification was developed for OI subtypes based on clinical features and disease severity. …”
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    Brittle Bone Disease: A Case Report
  17. 1237
    “…Osteogenesis imperfecta (OI) is a heritable connective tissue disorder that causes bone fragility due to pathogenic variants in genes responsible for the synthesis of type I collagen. …”
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    From Genetics to Clinical Implications: A Study of 675 Dutch Osteogenesis Imperfecta Patients
  18. 1238
    “…Out of the 13 SD categories modelled, OI profiles performed equally well or better than the volatile profiles for 11 of the SD, and across all SD the OI data was on average 21.9% more accurate (p = 0.031). …”
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    Utilisation of QSPR ODT modelling and odour vector modelling to predict Cannabis sativa odour
  19. 1239
    “…Osteogenesis imperfecta (OI) is an inherited congenital disorder, characterized primarily by decreased bone mass and increased bone fragility. …”
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    The recombinant BMP-2 loaded silk fibroin microspheres improved the bone phenotype of mild osteogenesis imperfecta mice
  20. 1240
    “…Significant differences between Groups I and II were found with respect to the presence or absence of 50 O-Islands (OIs) or S-loops and 13 K-islands (KIs) or K-loops, including the virulence-associated islands OI#1 (S-loop#1), OI#47 (S-loop#71), OI#57 (S-loop#85), OI#71 (S-loop#108), OI#115, OI#122, and OI#154 (S-loop#253). …”
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    Two distinct groups of porcine enteropathogenic Escherichia coli strains of serogroup O45 are revealed by comparative genomic hybridization and virulence gene microarray
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