Mostrando 821 - 840 Resultados de 20,093 Para Buscar '"recession"', tiempo de consulta: 0.34s Limitar resultados
  1. 821
  2. 822
    por Mukherji, Arnav
    Publicado 2016
    “…The use of guided tissue regeneration (GTR) procedures for the treatment of gingival recession has shown encouraging results and is gaining clinical acceptance. …”
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  3. 823
    “…These results not only present the ground data for the functional recovery of recessive AQP2 mutants through heteromerization, which prompt to revisit the accepted NDI model, but more importantly describe a general recovery process that could impact on all multimeric systems where recessive mutations are found.…”
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  4. 824
  5. 825
    “…CONCLUSIONS: Gingival recession in subjects with pre‐existing recession was significantly reduced after 3 years of brushing with either a power or manual toothbrush.…”
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  6. 826
    “…Autosomal recessive polycystic kidney disease (ARPKD) is a severe monogenic disorder that occurs due to mutations in the PKHD1 gene. …”
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  7. 827
    “…Our study delineates a unique form of recessive ASD and defines a role for CPAMD8, a protein of unknown function, in anterior segment development, implying another pathway for the pathogenicity of ASD.…”
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  8. 828
    por Lee, Dong Cheol, Lee, Se Youp
    Publicado 2017
    “…Recession and anteriorization were matched to vertical deviation in the primary position at far distance. …”
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  9. 829
  10. 830
  11. 831
  12. 832
    “…To evaluate the importance of TMPRSS3 mutations in recessive deafness among the Chinese, we screened 150 autosomal recessive nonsyndromic hearing loss (ARNSHL) families and identified 6 that carried seven causative TMPRSS3 mutations, including five novel mutations (c.809T>A, c.1151T>G, c.1204G>A, c.1244T>C, and c.1250G>A) and two previously reported mutations (c.323-6G>A and c.916G>A). …”
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  13. 833
    “…In this design, redox cycling occurs between the recessed disk and the top planar portion of a macroscopic thin film bipolar electrode in each nanopore. …”
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  14. 834
    “…Occasionally, bi‐allelic mutations in KCNQ1 are also found in patients without any deafness, referred to as autosomal recessive long QT syndrome, type 1 (AR LQT1). METHODS: We used Sanger sequencing to detect the pathogenic mutations in KCNQ1 gene in eight families from Saudi Arabia with autosomal recessive LQT1. …”
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  15. 835
    “…This is the first report of a unique autosomal recessive Inherited Palmoplantar keratoderma - sensorineural hearing loss syndrome which has not been reported before in 3 siblings of a large consanguineous family. …”
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  16. 836
  17. 837
    “…RESULTS: This study characterised the FJ spaces and recesses of the spine and found that (1) the configuration and extent of the FJ recesses varied along the spine. …”
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  18. 838
    “…Autosomal recessive bestrophinopathy (ARB) is caused by mutations in the gene BEST1 which encodes bestrophin 1 (Best1), an anion channel expressed in retinal pigment epithelial (RPE) cells. …”
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  19. 839
  20. 840
    “…This study aimed to describe the trends in horizontal inequity in the use of health services in Andalusia, Spain, during the early years of the Great Recession, and the contribution of demographic, economic and social factors. …”
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