Showing 81 - 100 results of 759 for search '"recession"', query time: 0.05s Refine Results
  1. 81
  2. 82
  3. 83

    Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family by Xia Wu, Shan Wang, Sen Chen, Ying-ying Wen, Bo Liu, Wen Xie, Dan Li, Lin Liu, Xiang Huang, Yu Sun, Wei-jia Kong

    Published 2018-01-01
    “…The two mutations are the first reported to be the cause of recessively inherited sensorineural hearing loss. Hearing loss levels and progression involved by PTPRQ mutations among the existing cases seem to be varied, and the relationship between genotypes and phenotypes is unclear. …”
    Get full text
    Article
  4. 84
  5. 85
  6. 86

    Recessive transition of rural residential land use from the perspective of value co-creation: A case study of Yiwu City, Zhejiang by ZHANG Cong, LONG Hualou, FENG Dedong

    Published 2025-01-01
    Subjects: “…value co-creation|recessive transition of land use|rural residential land redevelopment|yiwu…”
    Get full text
    Article
  7. 87

    Skeletal abnormalities caused by a Connexin43R239Q mutation in a mouse model for autosomal recessive craniometaphyseal dysplasia by Yasuyuki Fujii, Iichiro Okabe, Ayano Hatori, Shyam Kishor Sah, Jitendra Kanaujiya, Melanie Fisher, Rachael Norris, Mark Terasaki, Ernst J. Reichenberger, I-Ping Chen

    Published 2025-01-01
    “…Abstract Craniometaphyseal dysplasia (CMD), a rare craniotubular disorder, occurs in an autosomal dominant (AD) or autosomal recessive (AR) form. CMD is characterized by hyperostosis of craniofacial bones and metaphyseal flaring of long bones. …”
    Get full text
    Article
  8. 88
  9. 89

    Two-Stage Mucogingival Surgery with Free Gingival Autograft and Biomend Membrane and Coronally Advanced Flap in Treatment of Class III Millers Recession by Avita Rath, Smrithi Varma, Renny Paul

    Published 2016-01-01
    “…Introduction. Gingival recession is an apical shift of the gingival margin with exposure of the root surface. …”
    Get full text
    Article
  10. 90
  11. 91
  12. 92
  13. 93

    Clinical Comparison of the Subepithelial Connective Tissue versus Platelet-Rich Fibrin for the Multiple Gingival Recession Coverage on Anterior Teeth Using the Tunneling Technique by Victor Fabrizio Cabrera Pazmiño, Miguel Agusto Riquelme Rodas, Carlos David Barrios Cáceres, Guillermo Gustavo Renault Duarte, Melanie Vanesa Cano Azuaga, Bruna Luísa de Paula, Eliana Aparecida Caliente, Simone Soares, Elcia Maria Varize Silveira

    Published 2017-01-01
    “…The aim of this study was to evaluate and compare, clinically, the efficiency of the subepithelial connective tissue graft (SCTG) and platelet-rich fibrin (L-PRF) using the tunnel technique to cover the multiple gingival recessions on anterior teeth, in the same patient. Within the limits of this study, we conclude that both SCTG and L-PRF proved to be reliable options for the treatment of gingival recessions, efficiently supporting the biological and aesthetic demand, stimulating the periodontal tissues’ health, and bringing reliable and highly predictable results.…”
    Get full text
    Article
  14. 94
  15. 95

    Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families by Pengcheng Xu, Jun Xu, Hu Peng, Tao Yang

    Published 2020-01-01
    “…Auditory features of the affected individuals are consistent with that previously reported for recessive mutations in TMC1 and MYO15A. The two novel mutations identified in this study, p.M413T in TMC1 and p.R1407T in MYO15A, are classified as likely pathogenic according to the guidelines of ACMG. …”
    Get full text
    Article
  16. 96
  17. 97
  18. 98

    A Novel p.G141R Mutation in ILDR1 Leads to Recessive Nonsyndromic Deafness DFNB42 in Two Chinese Han Families by Xueling Wang, Longhao Wang, Hu Peng, Tao Yang, Hao Wu

    Published 2018-01-01
    “…Consistent with the recessive inheritance, cosegregation of the p.G141R variant with the hearing loss was confirmed in members of both families by PCR amplification and Sanger sequencing. …”
    Get full text
    Article
  19. 99
  20. 100