Browsing Otorhinolaryngology by Type "Postprint Article"

Browsing Otorhinolaryngology by Type "Postprint Article"

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  • The application of xylocaine 10% pump-spray to improve immediate post-adenotonsillectomy pain in children : a randomized controlled trial 
    Opperman, Jacobus B.; Tshifularo, Mashudu (Elsevier, 2022-10)
    INTRODUCTION : Post-adenotonsillectomy pain is often severe, requiring substantial analgesia in the first 48–72 h. This pain is not only distressing to the patient and his or her parents, but often reflects poorly on an ...
  • Blood otorrhea : blood stained sweaty ear discharges : Hematohidrosis; four case series (2001-2013) 
    Tshifularo, Mashudu (Elsevier, 2014-03)
    Hematohidrosis/hematidrosis/hemidrosis is a rare clinical condition in which human being sweats blood under condition of extreme physical or emotional stress [1. Jerajai HR, Bhagyashri Jaju, Phiske MM, and Nitin Lade. ...
  • The genetic basis of deafness in populations of African descent 
    Rudman, Jason R.; Kabahuma, Rosemary Ida; Bressler, Sara E.; Feng, Yong; Blanton, Susan H.; Yan, Denise; Liu, Xue-Zhong (Elsevier, 2017-06)
    Hearing loss is the most common sensorineural disorder worldwide and is associated with more than 1000 mutations in more than 90 genes. While mutations in genes such as GJB2 (gap-junction protein β 2) and GJB6 (gap-junction ...
  • Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents 
    Yan, Denise; Tekin, Demet; Bademci, Guney; Foster II, Joseph; Cengiz, F. Basak; Kannan‑Sundhari, Abhiraami; Guo, Shengru; Mittal, Rahul; Zou, Bing; Grati, Mhamed; Kabahuma, Rosemary Ida; Kameswaran, Mohan; Lasisi, Taye J.; Adedeji, Waheed A.; Lasisi, Akeem O.; Menendez, Ibis; Herrera, Marianna; Carranza, Claudia; Maroofian, Reza; Crosby, Andrew H.; Bensaid, Mariem; Masmoudi, Saber; Behnam, Mahdiyeh; Mojarrad, Majid; Feng, Yong; Duman, Duygu; Mawla, Alex M.; Nord, Alex S.; Blanton, Susan H.; Liu, Xue Z.; Tekin, Mustafa (Springer, 2016-08)
    Hearing loss is the most common sensory deficit in humans with causative variants in over 140 genes. With few exceptions, however, the population-specific distribution for many of the identified variants/genes is ...