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    Diverse Linguistic Development in Prelingually Deaf Children with Cochlear Implants by Pia De Stefano, Francesco Pisani, Giuseppe Cossu

    Published 2019-01-01
    “…This case series explores the variability of language acquisition in congenitally deaf children with cochlear implants. We report 4 prelingually deaf children (mean age=10.5; SD=1.08), affected by a genetically determined bilateral deafness, due to GJB2 gene mutation Cx26. …”
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  3. 63

    Magic in the ancient world: revealing antiquity 10 by F. Graf by S. P. J. K. Riekert

    Published 2003-06-01
    “…Dan is u reg ingestel om die werk van Graf aan te durf. Dit is ’n omvattende werk oor die toordery in die Hellenisties-Romeinse wêreld. …”
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    BRAF V600E-Negative Hairy Cell Leukaemia by Stephen E. Langabeer, David O'Brien, Anthony M. McElligott, Michelle Lavin, Paul V. Browne

    Published 2013-01-01
    “…Since the initial report of the BRAF V600E mutation in hairy cell leukemia, numerous investigators have demonstrated the presence of this activating mutation in nearly all cases of this disease. …”
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    Seizure, Deafness, and Renal Failure: A Case of Barakat Syndrome by Nasrollah Maleki, Bahman Bashardoust, Manouchehr Iranparvar Alamdari, Zahra Tavosi

    Published 2013-01-01
    “…Barakat syndrome (also known as HDR syndrome) is an autosomal dominant disorder characterized by hypoparathyroidism, sensorineural deafness, and renal disease caused by mutation of the GATA3 gene located at chromosome 10p15. …”
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  8. 68

    Grouting Reinforcement Mechanism and Multimodel Simulation Analysis of Longwall Goaf by Xueliang Li, Xiaoli Guo, Guang Sun

    Published 2021-01-01
    “…Grouting reinforcement is one of the most effective methods to enhance the stability of the goaf, and its scheme selection, hole location, and parameter determination directly affect the success or failure of goaf treatment. …”
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    Identification of Binding Partners of Deafness-Related Protein PDZD7 by Haibo Du, Rui Ren, Panpan Chen, Zhigang Xu, Yanfei Wang

    Published 2018-01-01
    “…PDZD7 is an important deafness gene, whose mutations are associated with syndromic and nonsyndromic hearing loss. …”
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    Auditory Hallucinations in a Deaf Patient: A Case Report by Natalia Pedersen, René Ernst Nielsen

    Published 2013-01-01
    “…This case report describes the progression of symptoms in a young deaf female. Her initial psychotic symptoms occur at the age of 16, but she did not come into contact with a psychiatric treatment facility before the age of 27, where she felt symptoms were distressing. …”
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  13. 73

    Knee phenotypes distribution according to CPAK classification in Turkish population by Vahit Emre Özden, Göksel Dikmen, Kayahan Karaytuğ, Arda Mavi, Yılmaz Onat Köylüoğlu, İsmail Remzi Tözün

    Published 2024-11-01
    “…Objective: This study aimed to investigate the distribution of knee phenotypes based on the CPAK classification in healthy nonarthritic subjects and osteoarthritic patients in Türkiye. …”
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    Yeşim Ustaoğlu Sinemasında Aile: Araf ve Tereddüt Filmlerinin Analizi by Semih Salman

    Published 2019-01-01
    “…Çalışmanın analiz bölümünde, hem filmlerin yakın zamanda kalıcı bir iz bırakmaları açısından hem de yönetmenin film dilinin belirgin yansımalarını daha net görebilmek amacıyla Araf ve Tereddüt filmleri tercih edilmektedir. Bu filmler, aile kavramı çerçevesinde analiz edilmektedir.…”
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  19. 79

    Research and response strategies on the impact of goaf collapse on overhead transmission lines by Siqing Xu, Xiaokai Meng, Shuai Wang, Zhumao Lu, Wen Shang

    Published 2025-01-01
    “…This article examines the impact of goaf collapse on overhead transmission lines, delving into various aspects such as foundation deformation, tower foundation and simulation calculation errors, tower deformation, and the effects at hanging points. …”
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