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  1. 1521
    “…BACKGROUND: Children with osteogenesis imperfecta (OI) can suffer from frequent fractures and limb deformities, resulting in impaired ambulation. …”
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    Results of a bone splint technique for the treatment of lower limb deformities in children with type I osteogenesis imperfecta
  2. 1522
    “…BACKGROUND AND PURPOSE: — Osteogenesis imperfecta (OI) is a heritable disorder of connective tissue caused by a defect in collagen type I synthesis. …”
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    Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up
  3. 1523
    “…[Image: see text] The complementary nature of positron emission tomography (PET) and optical imaging (OI) has fueled increasing interest in the development of multimodal PET/OI probes that can be employed during the diagnosis, staging, and surgical treatment of cancer. …”
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    Chemoenzymatic Strategy for the Synthesis of Site-Specifically Labeled Immunoconjugates for Multimodal PET and Optical Imaging
  4. 1524
    “…Objective: Since there is still controversy regarding the best first-line choice for ovulation induction (OI) other than clomiphene citrate (CC) in infertile women diagnosed with polycystic ovary syndrome (PCOS), the aim of the present study was to compare recombinant human FSH with CC as the first course of OI in these women. …”
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    Recombinant FSH Compared to Clomiphene Citrate as the First-Line in Ovulation Induction in Polycystic Ovary Syndrome Using Newly Designed Pens: A Randomized Controlled Trial
  5. 1525
    “…BACKGROUND: The aim of this study is to quantitatively evaluate the effect of rhBMP-2 for repair of bone defects after cyst enucleation using the osteogenesis index (OI). METHODS: Under general anesthesia, 10 patients (12 lesions) underwent oral or maxillofacial surgery for cyst enucleation. …”
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    Bone regenerative effect of recombinant human bone morphogenetic protein-2 after cyst enucleation
  6. 1526
    “…BACKGROUND: Osteogenesis imperfecta (OI) is a collagen-related bone dysplasia leading to a susceptibility to fractures. …”
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    Two novel compound heterozygous BMP1 mutations in a patient with osteogenesis imperfecta: a case report
  7. 1527
    “…The type I collagenopathies are a group of heterogeneous connective tissue disorders, that are caused by mutations in the genes encoding type I collagen and include specific forms of osteogenesis imperfecta (OI) and the Ehlers–Danlos syndrome (EDS). These disorders present with a broad disease spectrum and large clinical variability of which the underlying genetic basis is still poorly understood. …”
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    Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies
  8. 1528
    por Novak, Peter
    Publicado 2018
    “…The objective of the study was to identify markers of hypocapnic cerebral hypoperfusion (HYCH) in patients with orthostatic intolerance (OI) without tachycardia and without orthostatic hypotension. …”
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    Hypocapnic cerebral hypoperfusion: A biomarker of orthostatic intolerance
  9. 1529
    “…In Colombia, the OI and the OP—calculated by the CAC with data from the whole country—offer an opportunity for a more precise real-world estimation of patients with cancer in Colombia.…”
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    Incidence and Prevalence of Cancer in Colombia: The Methodology Used Matters
  10. 1530
    “…The genome of O157 contains 177 genomic islands known as O islands (OIs), including Shiga toxin-converting phages (OI-45 and OI-93) and the locus for enterocyte effacement (LEE) pathogenicity island (OI-148). …”
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    LysR-type transcriptional regulator OvrB encoded in O island 9 drives enterohemorrhagic Escherichia coli O157:H7 virulence
  11. 1531
    “…Osteogenesis Imperfecta (OI) is a rare inherited bone dysplasia, which is mainly caused by mutations in genes encoding type I collagen including COL1A1 and COL1A2. …”
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    Validation and Classification of Atypical Splicing Variants Associated With Osteogenesis Imperfecta
  12. 1532
    por Shinozaki, Kenji, Kawano, Naoki
    Publicado 2020
    “…The raw materials of OI crystal were impregnated into nanoporous glass having 4-nm pores and dried, obtaining a translucent sample of OI nanocrystals in glass (OIiG). …”
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    Rapid Synthesis of Quantum-Sized Organic–Inorganic Perovskite Nanocrystals in Glass
  13. 1533
    “…CASE SUMMARY: Osteogenesis imperfecta (OI) is an inherited disorder related to the synthesis of type 1 collagen. …”
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    Long-term follow-up of a cat with an undetermined osteoporotic bone disease managed with multiple intramedullary pins
  14. 1534
    “…The participants were dementia‐free and completed OI test using the Sniffin’ Sticks Screening Test‐12 at baseline. …”
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    Can dementia be predicted using olfactory identification test in the elderly? A Bayesian network analysis
  15. 1535
    por Miwa, Kunihisa, Inoue, Yukichi
    Publicado 2020
    “…BACKGROUND: Orthostatic intolerance (OI) markedly impairs activities of daily living in patients with myalgic encephalomyelitis (ME) or chronic fatigue syndrome. …”
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    Paradigm shift to disequilibrium in the genesis of orthostatic intolerance in patients with myalgic encephalomyelitis and chronic fatigue syndrome
  16. 1536
    “…BACKGROUND: Osteogenesis imperfecta (OI) is a rare heritable bone disorder that is characterised by increased bone fragility and recurrent fractures. …”
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    Novel mutations in BMP1 result in a patient with autosomal recessive osteogenesis imperfecta
  17. 1537
    “…OBJECTIVES: Osteogenesis Imperfecta (OI) is a heterogeneous condition mainly characterised by bone fragility; extra-skeletal features in OI include blue sclerae, dentinogenesis imperfecta, skin laxity and joint hyper-extensibility. …”
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    High bone mass phenotype in a cohort of patients with Osteogenesis Imperfecta caused due to BMP1 and C-propeptide cleavage variants in COL1A1
  18. 1538
    “…Osteogenesis imperfecta (OI) is an inherited genetic disorder characterized by frequent bone fractures and reduced bone mass. …”
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    A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta
  19. 1539
    “…Here we describe a previously unreported spontaneous vertebral reshaping in an adolescent with osteogenesis imperfecta (OI) with multiple vertebral fractures. CASE REPORT: A 17-year-old female was diagnosed with OI type I at 5 years of age caused by a novel frameshift variant in COL1A1 (NM_000088.4: c.540delC; p.Met181TrpfsTer84). …”
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    Spontaneous reshaping of vertebral fractures in an adolescent with osteogenesis imperfecta
  20. 1540
    “…After reviewing his medical history, he was suspected of having OI. The whole exome sequencing demonstrated a gene mutation in COL1A1 (OMIM 166200) and confirmed the diagnosis of OI. …”
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    Perthes Disease in a Child With Osteogenesis Imperfecta From a Rare Genetic Variant: A Case Report
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