Search Results - "STERN, Ryan E"

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  1. 1

    Analysis of free flap viability based on recipient vein selection by Francis, David O., Stern, Ryan E., Zeitler, Daniel, Izzard, Mark, Futran, Neal D.

    Published in Head & neck (01-10-2009)
    “…Background. Venous anastomotic failure is the primary reason for microvascular free tissue transfer failure. Donor and recipient veins can be oriented in the…”
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    Journal Article
  2. 2

    Aquaporin 4 expression in the mammalian inner ear and its role in hearing by Mhatre, Anand N, Stern, Ryan E, Li, Jiang, Lalwani, Anil K

    “…Aquaporin 4 (Aqp4), a member of a family of water transport proteins, is a candidate for playing a critical role in inner ear fluid homeostasis. In this study,…”
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    Journal Article
  3. 3

    Cochlear gene delivery through an intact round window membrane in mouse by Jero, J, Mhatre, A N, Tseng, C J, Stern, R E, Coling, D E, Goldstein, J A, Hong, K, Zheng, W W, Hoque, A T, Lalwani, A K

    Published in Human gene therapy (20-03-2001)
    “…Cochlear gene transfer studies in animal models have utilized mainly two delivery methods: direct injection through the round window membrane (RWM) or…”
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    Journal Article
  4. 4

    Recent Epidemiology of Pediatric Cochlear Implantation in the United States: Disparity Among Children of Different Ethnicity and Socioeconomic Status by Stern, Ryan E., Yueh, Bevan, Lewis, Charlotte, Norton, Susan, Sie, Kathleen C. Y.

    Published in The Laryngoscope (01-01-2005)
    “…Objectives/Hypothesis: Congenital severe to profound sensorineural hearing loss (SNHL) is found in higher proportions of children with minority and/or lower…”
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    Journal Article
  5. 5

    Audiologic evidence for further genetic heterogeneity at DFNA2 by STERN, Ryan E, LALWANI, Anil K

    Published in Acta oto-laryngologica (01-10-2002)
    “…A large American family has been mapped to the DFNA2 locus. However, mutation screening of CX31 and KCNQ4, the two genes associated with deafness at this…”
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    Journal Article
  6. 6

    Audiologic Evidence for Further Genetic Heterogeneity at DFNA2 by Stern, Ryan E., Lalwani, Anil K.

    Published in Acta oto-laryngologica (2002)
    “…A large American family has been mapped to the DFNA2 locus. However, mutation screening of CX31 and KCNQ4 , the two genes associated with deafness at this…”
    Get full text
    Journal Article