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  1. 1021
    “…Osteogenesis imperfecta (OI) is a genetic disease characterized by bone fragility and repeated fractures. …”
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    Online Artículo Texto
    Restoration of Osteogenesis by CRISPR/Cas9 Genome Editing of the Mutated COL1A1 Gene in Osteogenesis Imperfecta
  2. 1022
    “…Osteogenesis imperfecta (OI) is a heritable and chronically debilitating skeletal dysplasia. …”
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    Online Artículo Texto
    Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
  3. 1023
    “…A final evidence-based list of OI resulted by matching the adjudicated infections with the provisional list of OI. …”
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    Opportunistic infections in immunosuppressed patients with juvenile idiopathic arthritis: analysis by the Pharmachild Safety Adjudication Committee
  4. 1024
    “…Osteogenesis imperfecta (OI) is a hereditary disease occurring in humans and dogs. …”
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    A Missense Mutation in the SERPINH1 Gene in Dachshunds with Osteogenesis Imperfecta
  5. 1025
    “…However, as stricter regulations and environmental concerns are increasing over time, the importance of measuring OiW in real-time intensifies. The significant amount of uncertainties associated with manual samplings, that is currently not taken into consideration, could potentially affect the acceptance of OiW monitors and lower the reputation of all online OiW measurement techniques. …”
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    Online Artículo Texto
    Uncertainty Analysis of Fluorescence-Based Oil-In-Water Monitors for Oil and Gas Produced Water
  6. 1026
    “…Background: Osteogenesis imperfecta (OI) is a rare disease characterized by increased bone fragility and susceptibility for fractures. …”
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    Online Artículo Texto
    Incidence and treatment of adult femoral fractures with osteogenesis imperfecta: An analysis of a center of 72 patients in Taiwan
  7. 1027
    por Deng, Ying, Huo, Yanan, Li, Jinfeng
    Publicado 2021
    “…BACKGROUND: Osteogenesis imperfecta (OI) type V is a rare form of OI which is often characterized by hyperplastic callus. …”
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    Case Report: Hyperplastic Callus of the Femur Mimicking Osteosarcoma in Osteogenesis Imperfecta Type V
  8. 1028
    “…Osteogenesis imperfecta (OI) is a genetic disorder characterized by increased bone fragility and low bone mass, caused mainly by mutations in collagen type I encoding genes. …”
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    Online Artículo Texto
    Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children
  9. 1029
    “…There is no cure for osteogenesis imperfecta (OI), and current treatments can only partially correct the bone phenotype. …”
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    Online Artículo Texto
    A systematic review and meta-analysis on the efficacy of stem cell therapy on bone brittleness in mouse models of osteogenesis imperfecta
  10. 1030
    “…Osteogenesis Imperfecta (OI) is an inherited disorder characterized by extreme bone fragility due to collagen defects. …”
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    Online Artículo Texto
    Finite Element Prediction on Fracture Load of Femur with Osteogenesis Imperfecta under Various Loading Conditions
  11. 1031
    “…It has been validated for use in the United States (OI-US), United Kingdom (OI-UK) and Turkey (OI-TR). …”
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    Creating an Optimality Index – Netherlands: a validation study
  12. 1032
    “…Our long-term goal is to enhance communication of health and disease management findings back to the OI community, especially those who do not have access to major OI clinical centers. …”
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    Online Artículo Texto
    Assessing disease experience across the life span for individuals with osteogenesis imperfecta: challenges and opportunities for patient-reported outcomes (PROs) measurement: a pilot study
  13. 1033
    “…About 70% of people with osteogenesis imperfecta (OI) experience hearing loss. There is no cure for OI, and therapies to ameliorate hearing loss rely on conventional treatments for auditory impairments in the general population. …”
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    Online Artículo Texto
    Treatments for hearing loss in osteogenesis imperfecta: a systematic review and meta-analysis on their efficacy
  14. 1034
    “…Here, we aimed to develop novel biodegradable poly(DL-lactide-co-glycolic acid) phase-transition nanoparticles simultaneously loaded with oxygen and indocyanine green (OI-NPs) and to investigate the cytotoxic effects and the potential mechanisms of OI-NP–mediated PSDT on MH7A synoviocytes. …”
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    Online Artículo Texto
    Oxygen and indocyanine green loaded phase-transition nanoparticle-mediated photo-sonodynamic cytotoxic effects on rheumatoid arthritis fibroblast-like synoviocytes
  15. 1035
    “…Osteogenesis imperfecta (OI) is a rare heritable skeletal disorder which is mainly caused by defected type I collagen. …”
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    Online Artículo Texto
    Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta
  16. 1036
    “…Heritable connective tissue disorders such as osteogenesis imperfecta (OI) belong to this group. Herein, an affected calf showing congenital bone lesions such as intrauterine fractures, abnormally shaped long bones and localized arthrogryposis resembling OI type II is reported. …”
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    Online Artículo Texto
    A De Novo Mutation in COL1A1 in a Holstein Calf with Osteogenesis Imperfecta Type II
  17. 1037
    “…Different types of OI exist, from mild to severe; they may lead to death, multiple bone fractures, skeletal deformity and short stature. …”
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    Online Artículo Texto
    Radiographic features of osteogenesis imperfecta
  18. 1038
    “…Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous brittle bone disorder. …”
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    Online Artículo Texto
    Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans
  19. 1039
    “…RESULTS: Compared to controls, children with OI type I had lower muscle force and power. OI type I children were as active as their healthy counterparts. …”
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    Online Artículo Texto
    Physical activity in youth with osteogenesis imperfecta type I
  20. 1040
    “…In these attempts, the in vivo preclinical studies are of paramount importance; therefore, serious analysis is required to choose the right murine OI model able to emulate as closely as possible the disease of the target OI population. …”
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    Online Artículo Texto
    Murine Animal Models in Osteogenesis Imperfecta: The Quest for Improving the Quality of Life
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