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  1. 1461
    “…Purpose: This study aim was to compare the effectiveness of the median nerve neural mobilization (MNNM) and cervical lateral glide (CLG) intervention versus oral ibuprofen (OI) in subjects who suffer cervicobrachial pain (CP). …”
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    Is pharmacologic treatment better than neural mobilization for cervicobrachial pain? A randomized clinical trial
  2. 1462
    “…Classical osteogenesis imperfecta (OI) is a bone disease caused by type I collagen mutations and characterized by bone fragility, frequent fractures in absence of trauma and growth deficiency. …”
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    The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta
  3. 1463
    “…OBJECTIVES: Osteogenesis Imperfecta (OI) is a heterogeneous condition mainly characterised by bone fragility; intelligence is reported to be normal. …”
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    Online Artículo Texto
    Autism and heritable bone fragility: A true association?
  4. 1464
    “…We aimed to evaluate efficacy of ozone injection (OI) in MPS patients, compared with two currently used methods including lidocaine injection (LI) and dry needling (DN). …”
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    Comparison of ozone and lidocaine injection efficacy vs dry needling in myofascial pain syndrome patients
  5. 1465
    “…INTRODUCTION: Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disease with skeletal fragility and variable extra-skeletal manifestations. …”
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    Online Artículo Texto
    Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta
  6. 1466
    “…BACKGROUND: A Diagnostic Laboratory Hub (DLH) was set up in Guatemala to provide opportunistic infection (OI) diagnosis for people with HIV (PWH). METHODS: Patients newly presenting for HIV, PWH not receiving antiretrovirals (ARVs) for >90 days but returned to care (Return/Restart), and PWH on ARVs with symptoms of OIs (ARV treatment) were prospectively included. …”
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    The Diagnostic Laboratory Hub: A New Health Care System Reveals the Incidence and Mortality of Tuberculosis, Histoplasmosis, and Cryptococcosis of PWH in Guatemala
  7. 1467
    “…The mutation in WNT1 causes autosomal recessive OI (AR‐OI) due to the key role of WNT/β‐catenin signaling in bone formation. …”
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    The role of WNT1 mutant variant (WNT1(c.677C>T)) in osteogenesis imperfecta
  8. 1468
    “…Osteogenesis imperfecta (OI) and other decreased bone density disorders comprise a heterogeneous group of heritable diseases with skeletal fragility. …”
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    A Novel IFITM5 Variant Associated with Phenotype of Osteoporosis with Calvarial Doughnut Lesions: A Case Report
  9. 1469
    por Daripa, Bob, Lucchese, Scott
    Publicado 2022
    “…Increased susceptibility to opportunistic infections (OI) in multiple sclerosis (MS) patients is a real concern amongst neurologists when using disease-modifying therapies (DMTs). …”
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    Varicella-Zoster Reactivation in a Non-immunized Elderly Multiple Sclerosis Patient While on Delayed-Release Dimethyl Fumarate With Grade 2 Lymphopenia and Profoundly Low CD4+ and CD8+ Cell Counts: A Case Report
  10. 1470
    “…BACKGROUND: Osteogenesis imperfecta (OI) is a rare heterogeneous disorder typically featured by fragile bones and susceptibility to fracture. …”
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    Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing
  11. 1471
    “…Similarly, the P300 amplitudes following outcome feedback were larger in the CI group than that in the OI group with gain feedback and had no significant difference between OE and OI.…”
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    The Effect of Social Exclusion on Trust Among Youth Orphaned by HIV/AIDS: Evidence From an Event-Related Potentials Study
  12. 1472
    “…Of the remaining patients, only 1 woman successfully delivered after a cycle of ovulation induction with intrauterine insemination (OI/IUI). Other patients pursuing OI/IUI, OI/TIC, or monitored natural cycles had unsuccessful experiences. …”
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    Fumarase Deficiency and Its Effect on Infertility: A Case Series
  13. 1473
    “…RESULTS: Receiver-operator curve analysis demonstrated that the E(2)/P ratio could differentiate between clinical pregnancies and non-pregnant cycles (area under the curve on OI +4 days = 0.70; 95% CI = 0.60–0.80; p = 0.003, on OI +5 days = 0.76; 95% CI = 0.64–0.88; p = 0.001, OI +7 days = 0.85; 95% CI = 0.75–0.96; p < 0.0001). …”
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    Serum estradiol/progesterone ratio on day of embryo transfer may predict reproductive outcome following controlled ovarian hyperstimulation and in vitro fertilization
  14. 1474
    “…In the absence of differences between OI and IT conditions, BI mice exhibited half as much Paw-licking behavior than OI group. …”
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    A Trouble Shared Is a Trouble Halved: Social Context and Status Affect Pain in Mouse Dyads
  15. 1475
    “…Moreover, complete excision of the islands occurred by site-specific recombination between flanking direct repeats. Complete excision of OI 43 and OI 48 occurred in 1.81 × 10(−3) and 1.97 × 10(−4) cells in culture, respectively; internal deletion of OI 48 was more frequent (9.7 × 10(−1) cells). …”
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    Chromosomal instability in enterohaemorrhagic Escherichia coli O157:H7: impact on adherence, tellurite resistance and colony phenotype
  16. 1476
    “…Our study thus highlights the phenotypic variability of OI type V caused by the IFITM5 mutation.…”
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    Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM5 Mutation
  17. 1477
    “…Ultrasound images of the LM, TrA, OI, and obliquus externus (OE) were captured during stimulation at each frequency. …”
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    Activations of Deep Lumbar Stabilizing Muscles by Transcutaneous Neuromuscular Electrical Stimulation of Lumbar Paraspinal Regions
  18. 1478
    “…BACKGROUND: Joint hypermobility is a common clinical characteristic of patients with Osteogenesis imperfecta (OI), a disorder with serious comorbidities of scoliosis and cranial base anomalies. …”
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    Association between joint hypermobility, scoliosis, and cranial base anomalies in paediatric Osteogenesis imperfecta patients: a retrospective cross-sectional study
  19. 1479
    “…Osteogenesis imperfecta (OI) is a hereditary bone fragility disorder that in most patients is caused by mutations affecting collagen type I. …”
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    A cephalometric method to diagnosis the craniovertebral junction abnormalities in osteogenesis imperfecta patients
  20. 1480
    “…Osteogenesis imperfecta (OI) is a rare genetic disorder of type I collagen. …”
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    Developmental charts for children with osteogenesis imperfecta, type I (body height, body weight and BMI)
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