• Proceedings of the KSLP Conference
• /
• 2015.03a
• /
• pp.20-20
• /
• 2015

• Proceedings of the KSLP Conference
• /
• 2006.12a
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• pp.167-167
• /
• 2006

• Proceedings of the KSLP Conference
• /
• 1999.11a
• /
• pp.178-178
• /
• 1999

배경 : 치유 과정에서 성대점막에 반흔을 형성하여 영구히 음성변화를 유발시킬 수도 있는 성대 점막하 출혈은 드물지 않게 접하게 되는 질환이지만, 이것에 대한 자세한 연구는 많지가 않았다. 목적 : 저자들은 성대 저막하 출혈을 만들어 낼 수 있는 원인과 이것에 영향을 주게 되는 요소들이 어떤 것인지 알아보기 위하여 본 연구를 시작하였다. (중략)

• Proceedings of the KSLP Conference
• /
• 2012.03a
• /
• pp.22-22
• /
• 2012

• Proceedings of the KSLP Conference
• /
• 2012.03a
• /
• pp.35-35
• /
• 2012

• Proceedings of the KSLP Conference
• /
• 2013.03a
• /
• pp.15-15
• /
• 2013

• Proceedings of the KSLP Conference
• /
• 2015.03a
• /
• pp.38-38
• /
• 2015

• Proceedings of the KSLP Conference
• /
• 1999.11a
• /
• pp.176-176
• /
• 1999

배경 : trill은 혀의 첨부가 호기에 따라 진동하면서 경구개 전방에 부딪혀 나는 소리로 주로 "르" 발음으로 들린다. trill은 성악가들에게는 발성전에 후두의 준비운동으로 사용되고, 성대수술 반흔에 의한 애성환자나 노인성 음성장애환자의 음성치료에도 이용되고 있다. 목적 : trill을 실시할 때 전기성문파 측정법상에서 나타난 성대점막의 움직임을 조사하고 효과적인 trill 기법을 찾아보고자 하였다. (중략)

• Journal of the Korean Society of Laryngology, Phoniatrics and Logopedics
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• v.25 no.1
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• pp.36-38
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• 2014

The patient suffered cardiac arrest 8 months before presentation. She has been suffering hoarseness and exertional dyspnea and nocturnal stridor. Upon flexible laryngoscopy, her vocal cords showed no motion and fixed in paramedian position. There was no causal finding on neck CT. EMG showed some muscular activity. Under the suspicion of crico arytenoid fixation, we performed suspension laryngoscopy, and found the arytenoid cartilage was fixed with short and stout scar, which was removed with scissors. Just after surgery she regained her voice and respiration.

• Journal of the Korean Society of Laryngology, Phoniatrics and Logopedics
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• v.23 no.1
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• pp.28-32
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• 2012

Vocal fold scar disrupts structure of lamina propria and causes significant change in vocal fold tissue biomechanics, resulting in a range of voice problems that often significantly compromise patient quality of life. Although several therapeutic management have been offered in an attempt to improve vocal fold scar, the ideal treatment has not yet been found. Recently, several tissue engineering technique for vocal fold scar using growth factors, several cells, and scaffolds have been described in tissue culture and animal models. Several growth factors such as hepatocyte growth factor, basic fibroblast growth factor, and transforming growth factor beta 3 for therapy and prevention of vocal fold scar have been studied. Cell types to regenerate vocal folds in scarring tissue have been introduced autologous or scarred vocal fold fibroblast and adult mesenchymal stem cells. Decellularized organ matrix and several hyaluronic acid materials have used as scaffolds for vocal fold scar.