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Mostrando 961 - 980 Resultados de 3,184 Para Buscar '"Oi!"', tiempo de consulta: 0.17s Limitar resultados
  1. 961
    “…(1) Background: Odor identification (OI) dysfunction is a potential predictor of developing dementia in late life depression (LLD). …”
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    Differences in Odor Identification in Early-Onset and Late-Onset Depression
  2. 962
    “…However, the long-term effects of OI alone on offspring health have not been studied. …”
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    MON-LB001 Ovulation Induction Results in Altered Growth and Metabolic Dysfunction in Mice Offspring
  3. 963
    “…All patients with an AIDS-defining OI were included. In patients with more than one OI the first event reported was considered. …”
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    Time to HAART Initiation after Diagnosis and Treatment of Opportunistic Infections in Patients with AIDS in Latin America
  4. 964
    “…Sclerostin antibody (SclAb) therapy has been suggested as a novel therapeutic approach toward addressing the fragility phenotypic of osteogenesis imperfecta (OI). Observations of cellular and transcriptional responses to SclAb in OI have been limited to mouse models of the disorder, leaving a paucity of data on the human OI osteoblastic cellular response to the treatment. …”
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    Gene Expression Profile and Acute Gene Expression Response to Sclerostin Inhibition in Osteogenesis Imperfecta Bone
  5. 965
    “…BACKGROUND: Osteogenesis imperfecta (OI) affects dental and craniofacial development and may therefore impair Oral Health-Related Quality of Life (OHRQoL). …”
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    Oral health-related quality of life in children and adolescents with osteogenesis imperfecta: cross-sectional study
  6. 966
    “…RESULTS: Ninety-nine patients (OI type 1 (n = 72), OI type 3 (n = 13), OI type 4 (n = 14) completed the FSS questionnaire. …”
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    Fatigue in adults with Osteogenesis Imperfecta
  7. 967
    “…BACKGROUND: Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mineral density and fractures. …”
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    Health-related quality of life of children and adolescents with osteogenesis imperfecta: a cross-sectional study using PedsQL™
  8. 968
    “…Osteogenesis imperfecta (OI) is a rare genetic disorder also known as a “brittle bone disease.” …”
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    Inter‐ and Intrafamilial Phenotypic Variability in Individuals with Collagen‐Related Osteogenesis Imperfecta
  9. 969
    “…Oxidative stress, inflammation, and apoptosis are crucial in the pathogenesis of acute liver failure (ALF). 4-Octyl itaconate (OI) showed antioxidative and anti-inflammatory properties in many disease models. …”
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    Protective Role of 4-Octyl Itaconate in Murine LPS/D-GalN-Induced Acute Liver Failure via Inhibiting Inflammation, Oxidative Stress, and Apoptosis
  10. 970
    “…The aim is to recommend a minimum standard set of clinician-reported outcome measures (CROMs) and patient-reported outcome measures (PROMs) on hearing for people with osteogenesis imperfecta (OI). This project is part of the larger “Key4OI” project initiated by the “Care4BrittleBones foundation” of which the goal is to improve quality of life of people with OI. …”
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    The International Standard Set of Outcome Measures for the Assessment of Hearing in People with Osteogenesis Imperfecta
  11. 971
    “…However, neuropsychiatric symptoms (NPSs) are common in LLD and are associated with OI deficits. In subjects with LLD, when OI deficits forecast cognitive decline, whether and how NPS affects the relationship between OI and cognition still must be further explored. …”
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    Interactive Effects of Agitation and Cognitive Impairment on Odor Identification in Patients With Late-Life Depression
  12. 972
    “…Using a cross-lagged panel design with two measurement times, Study 1 examined the directionality of the relationship between OI and AC, and showed that OI is positively related to temporal change in AC, confirming the antecedence of OI on AC. …”
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    Employees’ Organizational Identification and Affective Organizational Commitment: An Integrative Approach
  13. 973
    por Plotkin, Horacio
    Publicado 2004
    “…BACKGROUND: There is no clear definition of osteogenesis imperfecta (OI). The most widely used classification of OI divides the disease in four types, although it has been suggested that there may be at least 12 forms of OI. …”
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    Syndromes with congenital brittle bones
  14. 974
    “…To explore the role of BH4 in ME/CFS, serum samples of CFS patients (n = 32), CFS patients with OI only (n = 10; CFS + OI), and CFS patients with both OI and small fiber polyneuropathy (n = 12; CFS + OI + SFN) were subjected to BH4 ELISA. …”
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    Detection of Elevated Level of Tetrahydrobiopterin in Serum Samples of ME/CFS Patients with Orthostatic Intolerance: A Pilot Study
  15. 975
    “…BACKGROUND: Osteogenesis imperfecta (OI) is a rare genetic disorder that causes increased bone fragility. …”
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    The impact of severe osteogenesis imperfecta on the lives of young patients and their parents – a qualitative analysis
  16. 976
    “…Osteogenesis imperfecta (OI) is a heritable brittle bone disease mainly caused by mutations in the two type I collagen genes. …”
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    4-Phenylbutyric acid enhances the mineralization of osteogenesis imperfecta iPSC-derived osteoblasts
  17. 977
    “…OBJECTIVE: Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disease characterized by recurrent fractures, blue sclera, and hearing loss. …”
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    Effects of Long-Term Pamidronate Treatment on Bone Density and Fracture Rate in 65 Osteogenesis Imperfecta Patients
  18. 978
    “…OBJECTIVE: The objective of the current study is to assess the effect of a seven-week voluntary wheel running intervention on muscles and bones properties in a mouse model mimicking dominant severe osteogenesis imperfecta (OI). METHODS: Female wild-type (WT) and OI (Col1a1(Jrt/+)) mice either performed voluntarily wheel-running exercise for 7-weeks or remained sedentary. …”
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    Muscle-bone properties after prolonged voluntary wheel running in a mouse model of dominant severe osteogenesis imperfecta
  19. 979
    “…BACKGROUND: Osteogenesis Imperfecta (OI) is a rare genetic disorder involving bone fragility. …”
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    Reproductive options for families at risk of Osteogenesis Imperfecta: a review
  20. 980
    “…Based on this concept, we performed a functional proteomic study to delineate affected molecular pathways in primary fibroblasts from recessive OI patients, carrying mutations in CRTAP (OI type VII), P3H1 (OI type VIII), and PPIB (OI type IX) genes. …”
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    Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective
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