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  1. 1041
    “…PURPOSE: Osteogenesis imperfecta (OI) predisposes to recurrent fractures. The moderate-to-severe forms of OI present with antenatal fractures and the mode of delivery that would be safest for the fetus is not known. …”
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    Delivery by Cesarean Section is not Associated With Decreased at-Birth Fracture Rates in Osteogenesis Imperfecta
  2. 1042
    “…BACKGROUND: The long-term effects of occupational injury (OI) on psychiatric diseases are unclear. This study assessed and compared the effects of OI, no injury (control), and non-OI (NOI) on the development of psychiatric diseases. …”
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    Occupational and Non-occupational Injuries Can Result in Prolonged Augmentation of Psychiatric Disorders
  3. 1043
    “…As a specific activator of nuclear factor E2-related factor 2 (Nrf2), the 4-octyl itaconate (4-OI) has the beneficial effects in antioxidant and anti-inflammation; however, whether 4-OI can alleviate hepatic steatosis and its mechanism is still unknown. …”
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    4-Octyl Itaconate Prevents Free Fatty Acid-Induced Lipid Metabolism Disorder through Activating Nrf2-AMPK Signaling Pathway in Hepatocytes
  4. 1044
    “…Osteogenesis imperfecta (OI) is an inherited skeletal dysplasia characterized by low bone density, bone fragility and recurrent fractures. …”
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    Omics Profiling of S2P Mutant Fibroblasts as a Mean to Unravel the Pathomechanism and Molecular Signatures of X-Linked MBTPS2 Osteogenesis Imperfecta
  5. 1045
    “…RESULTS: The P-BD and NP-BD groups exhibited impaired OI compared with the HC group, but there was no significant difference in OI between the P-BD and NP-BD groups, or in OS among all three groups. …”
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    Impaired olfactory function in bipolar disorder patients during acute episodes regardless of psychotic symptoms
  6. 1046
    “…The diagnosis of OI is easily missed in its mild form. Early diagnosis is important, and there is a need for improved awareness of OI among health care professionals. …”
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    Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene causing osteogenesis imperfecta
  7. 1047
    “…WB and qPCR were used to verify the effect of 4-OI on inflammation and oxidative stress caused by MRSA. …”
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    Itaconate ameliorates methicillin-resistant Staphylococcus aureus-induced acute lung injury through the Nrf2/ARE pathway
  8. 1048
    “…Pediatric patients with Osteogenesis Imperfecta (OI), a heritable connective tissue disorder, frequently suffer from long bone deformations. …”
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    Characterization and functional analysis of the adipose tissue-derived stromal vascular fraction of pediatric patients with osteogenesis imperfecta
  9. 1049
    “…We describe a case of siblings who presented with metaphyseal corner fractures and multiple posterior rib fractures who were later found to carry FKBP10 mutations, a rare cause of Osteogenesis Imperfecta (OI) known as Bruck syndrome. This clinical presentation led to a literature review examining fracture types in OI and inflicted injury. …”
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    Metaphyseal and posterior rib fractures in osteogenesis imperfecta: Case report and review of the literature
  10. 1050
    “…Osteogenesis imperfecta (OI) is a hereditary disorder characterized by increased tendency for bone fractures due to high fragility. …”
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    Osteogenesis Imperfecta (Type IV) with Dental Findings in Siblings
  11. 1051
    “…Bone fragility and skeletal irregularities are the characteristic features of osteogenesis imperfecta (OI). Many patients with OI have weakened maxillary and mandibular bone, leading to poor oral hygiene and subsequent loss of teeth. …”
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    Implant therapy for a patient with osteogenesis imperfecta type I: review of literature with a case report
  12. 1052
    “…The prevalence of hip dysplasia and OI was therefore 0.87% (per patient). In 4 of the 5 patients (80%), OI was caused by mutations affecting the C-propeptide of collagen type I, which is otherwise rare in OI. …”
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    Hip Dysplasia in Children With Osteogenesis Imperfecta: Association With Collagen Type I C-Propeptide Mutations
  13. 1053
    por Zhao, Xuemin, Bie, Mengjun
    Publicado 2020
    “…BACKGROUND: Acute aortic dissection (AAD) is an acute life-threatening cardiovascular disease, which is frequently complicated with oxygenation impairment (OI). We aim to investigate predictors of the development of OI in the patients with AAD. …”
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    Predictors for the development of preoperative oxygenation impairment in acute aortic dissection in hypertensive patients
  14. 1054
    “…Osteogenesis imperfecta (OI) is a rare genetic disorder associated with low bone density and increased bone fragility. …”
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    Use of Netnography to Understand GoFundMe(®) Crowdfunding Profiles Posted for Individuals and Families of Children with Osteogenesis Imperfecta
  15. 1055
    “…Background: Osteogenesis imperfecta (OI) and transplantation (TP) are independently associated with fractures. …”
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    Lung Transplantation in a Patient With Osteogenesis Imperfecta and Osteoporosis
  16. 1056
    “…However, the influence of BPV in orthostatic intolerance (OI) is unknown. Herein, we assessed BPV profiles in patients with OI and determined their association with orthostatic symptoms. …”
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    Association of blood pressure variability with orthostatic intolerance symptoms
  17. 1057
    “…PURPOSE: Osteogenesis imperfecta (OI) is a heritable skeletal dysplasia. Dominant pathogenic variants in COL1A1 and COL1A2 explain the majority of OI cases. …”
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    Monoallelic and Biallelic CREB3L1 Variant Causes Mild and Severe Osteogenesis Imperfecta, Respectively
  18. 1058
    “…Of the 12 patients, 4 had no OI and 8 had a clinical suspicion of OI. In 8 patients with OI, absolute blood volumes were significantly lower than for the 4 without OI (56 [2] vs. 66 [5]; p < 0.05) as were the differences between the measured and the reference blood volume (−14 [2]; vs. −4 [3]; p < 0.02). …”
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    Blood Volume Status in ME/CFS Correlates With the Presence or Absence of Orthostatic Symptoms: Preliminary Results
  19. 1059
    “…BACKGROUND: Patients with Osteogenesis imperfecta (OI) suffer from increased bone fracture tendency generally caused by a mutation in genes coding for type I collagen. …”
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    Is sleep apnea underdiagnosed in adult patients with osteogenesis imperfecta? –a single-center cross-sectional study
  20. 1060
    “…Osteogenesis imperfecta (OI) is mainly characterized by bone fragility and Ehlers-Danlos syndrome (EDS) by connective tissue defects. …”
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    A novel mutation in COL1A2 leads to osteogenesis imperfecta/Ehlers-Danlos overlap syndrome with brachydactyly
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