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  1. 1281
    “…BACKGROUND: Osteogenesis imperfecta (OI) is a rare connective‐tissue disorder characterized by bone fragility. …”
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    Genetic analysis in Japanese patients with osteogenesis imperfecta: Genotype and phenotype spectra in 96 probands
  2. 1282
    “…The bone disorder osteogenesis imperfecta (OI) is genetically heterogeneous. Most affected individuals have an autosomal dominant disorder caused by heterozygous variants in either of the type I collagen genes (COL1A1 or COL1A2). …”
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    Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta
  3. 1283
    “…In the present study, clinical manifestations and genetic variants were analysed from 187 Chinese OI patients, majority of whom are of southern Chinese origin. …”
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    Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen
  4. 1284
    por Zhao, Xuemin, Bie, Mengjun
    Publicado 2022
    “…Acute lung injury (ALI) and oxygenation impairment (OI) frequently occur in the patients with acute aortic dissection (AAD), which may necessitate mechanical ventilation and result in adverse outcomes. …”
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    Preoperative acute lung injury and oxygenation impairment occurred in the patients with acute aortic dissection
  5. 1285
    “…INTRODUCTION: To evaluate sildenafil citrate as an adjuvant to clomiphene citrate (CC) for ovulation induction (OI) in women with polycystic ovary syndrome (PCOS). …”
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    Sildenafil citrate as an adjuvant to clomiphene citrate for ovulation induction in polycystic ovary syndrome: crossover randomized controlled trial
  6. 1286
    “…Results: After the effective encapsulation of 4-OI, 4-OI@Zn-NH-pyr not only exhibited potent ROS-scavenging capacity, but also reduced ROS production by mediating mitochondrial respiration in inflammatory macrophages. …”
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    Mitochondria-targeted supramolecular coordination container encapsulated with exogenous itaconate for synergistic therapy of joint inflammation
  7. 1287
    “…BACKGROUND: Osteogenesis imperfecta type I (OI‐I) is a rare genetic disorder characterized by skeletal deformity, bone fragility, blue sclerae, dentinogenesis imperfecta, and hearing loss. …”
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    Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I
  8. 1288
    “…RESULTS: A total of 588 (mild TBI = 307; OI = 281) eligible children were approached in the ED and 315 (mild TBI = 195; OI = 120) were consented. …”
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    Social determinants of participant recruitment and retention in a prospective cohort study of pediatric mild traumatic brain injury
  9. 1289
    “…These results indicate that 4-OI lowers macrophage inflammation, likely promoting a more wound-resolving phenotype.…”
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    Itaconate promotes a wound resolving phenotype in pro-inflammatory macrophages
  10. 1290
    “…OBJECTIVES: To screen the COL1A1 and COL1A2 gene mutation sites in a family with type I osteogenesis imperfecta (OI)/hearing loss and analyze the characteristics and recovery of hearing loss in patients with osteogenesis imperfecta. …”
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    A novel mutation in COL1A1 causing osteogenesis imperfecta/hearing loss
  11. 1291
    “…Subjects underwent five fMRI scanning paradigms: one with heat pain (HP), two with OI-EA and MI-EA, and two with OI-EA and HP, and MI-EA and HP. …”
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    The analgesic effect of electroacupuncture on acute thermal pain perception-a central neural correlate study with fMRI
  12. 1292
    “…Osteogenesis imperfecta (OI) is an inheritable bone disorder characterized by osseous fragility and ligamentous laxity. …”
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    THE SURGICAL TREATMENT METHOD FOR AN ADULT POSTTRAUMATIC THORACOLUMBAR KYPHOSIS PATIENT WITH OSTEOGENESIS IMPERFECTA
  13. 1293
    “…Symptoms of orthostatic intolerance (OI) are common in Chronic Fatigue Syndrome (CFS) and similar disorders. …”
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    Intracranial compliance is associated with symptoms of orthostatic intolerance in chronic fatigue syndrome
  14. 1294
    “…Osteogenesis imperfecta (OI) is an inherited connective tissue disorder characterized by bone fragility and is characterized by clinical and genetic heterogeneity. …”
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    Expanding the Clinical Spectrum of Osteogenesis Imperfecta Type V: 13 Additional Patients and Review
  15. 1295
    por Wu, Dong, Wang, Yuxin, Huang, Huijuan
    Publicado 2020
    “…BACKGROUND: Osteogenesis imperfecta (OI) type V is a rare heritable bone disorder caused by pathogenic variants of IFITM5. …”
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    A novel variant of the IFITM5 gene within the 5′‐UTR causes neonatal transverse clavicular fracture: Expanding the genetic spectrum
  16. 1296
    “…The results for the V(s) of the OE and OI in the right trunk rotation suggest that surface EMG electrodes placed on the OE would detect not only the antagonistic OE activity but also the agonistic OI activity.…”
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    Verification of surface electromyographic activity of the oblique externus abdominis using ultrasound shear wave elastography
  17. 1297
    por Chen, Hong
    Publicado 2022
    “…Substantial intellectual property management (IPM) is vital in retaining competitive advantage and managing outbound open innovation (OI), which may enhance an organization’s commercialization and entrepreneurial performance. …”
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    The impact of intellectual property protection on the development of digital economy and regional entrepreneurial activity: Evidence from small and medium enterprises
  18. 1298
    “…We propose an ornamentation index (OI) derived from 3D scanning technology and a virtual model for quantifying ornamentation complexity. …”
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    A new index for quantifying the ornamentational complexity of animals with shells
  19. 1299
    “…Lamellar bone formed in individuals with moderate and severe osteogenesis imperfecta (OI) is often composed of lamellae that are structurally abnormal. …”
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    Automated measurement of lamellar thickness in human bone using polarized light microscopy
  20. 1300
    “…DI type I is associated with osteogenesis imperfect (OI), which is an inheritable disorder of connective tissue. …”
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    Brittle teeth with brittle bone in a family for four generations: Case report and literature review
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