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主办单位:

解放军总医院耳鼻咽喉头颈外科医院
 
协办单位:
 
生物芯片北京国家工程研究中心
 
澳麦尔基因技术有限公司

主席致辞

          亲爱的同行朋友们，欢迎亲临2009年耳聋与基因医学国际研讨会！
对于我们所有人来说，这是与世界耳聋遗传学界同行交流与分享最新研究发现的好机会。毋庸置疑，在研讨会上知识的碰撞与交流必将促进耳聋基因医学的进一步发展。

 

注册信息

报到时间：2009年8月28日（星期五）全天报到

报到地点：北京美泉宫饭店大厅（北京西四环的四季青桥南侧）

大堂电话：010-88869999

网         址：
http://www.schonbrunnbj.com

会议时间：2009年8月29日-30日

会议地点：北京解放军总医院外科大楼17层会议中心
 
会议语言：英语（同声传译）

联系电话：010-66936753-608
 
会务组：王国建    韩    冰   康东洋 
                 卢    宇   金占国   朱玉华
 
手    机：13146469952(王国建)
                 13301256629(韩   冰)
 
              daisy9716@yahoo.com.cn
 
注册费用：500元，安排食宿，费用自理。
 
联系地址：北京市复兴路28号解放军总医院耳鼻喉研究所(100853) 
 

 

访问统计

今日访问量: 5
总访问量: 5065
最大月访问量: 1515
最大月访问量发生时间: 2009-8
统计起始时间: 2009-07-25
Simon I. Angeli 教授

        Simon博士现为迈阿密大学医学院耳鼻喉科教授。他于1987年毕业于委内瑞拉中央大学，随后在美国爱荷华大学医学院及临床中心的耳鼻咽喉头颈外科，以及众议院耳诊所神经耳科学继续学习和工作。 他的主要研究方向：1）遗传性耳聋表型和基因型的转化学研究；非综合症性耳聋和老年性聋的分子筛查。2）氧化应激在突发性感音神经性聋中的作用，分析参与氧化应激反应酶的多态性及抗氧化治疗的临床疗效。3）中耳炎及耳硬化的手术治疗，中耳伤口愈合中透明质酸凝胶的应用。4）人工耳蜗植入术效果、手术及创伤预防的研究。5）前庭功能异常及其临床疗效。6）听神经瘤手术及疗效。

 

CURRICULUM VITAE
 
NAME： SIMON I. ANGELI
 
Current position:    Professor of Clinical Otolaryngology, University of Miami School of Medicine, Miami, Florida, U.S.A.
 
Education:
Fellowship:         House Ear Clinic, Los Angeles, California
July 1994 – June 1995
Neurotologic Skull Base Surgery
Residency:          University of Iowa Hospitals and Clinics, Iowa City, Iowa
July 1990 – June 1994
Otolaryngology-Head and Neck Surgery
Research Fellowship: University of Iowa Hospitals and Clinics, Iowa City, Iowa
July 1989 – June 1990
Otolaryngology-Head and Neck Surgery
Internship:                 University of Iowa Hospitals and Clinics, Iowa City, Iowa
July 1988 – June 1989
General Surgery
Medical School: Universidad Central de Venezuela, Caracas, Venezuela
September 1980 – December 1986
Date of graduation: March 7th, 1987
 
Research Interests:
Translational research in hereditary deafness, phenotype/genotype correlations; molecular screening for nonsyndromic deafness and presbycusis.
Role of oxidative stress in sudden sensorineural hearing loss, analysis of polymorphisms of enzymes involved in oxidative stress and clinical response to treatment with antioxidants (funded clinical trial).
Middle ear surgery for otitis media and otosclerosis, use of hyaluronic acid gel for middle ear wound healing (funded research)
Cochlear implantation outcomes, surgery, avoidance of trauma.
Vestibular disorders, clinical outcomes
Acoustic neuroma surgery and outcome.
 
Selected Publications:
1.        Bared A, Angeli SI. Malleus handle: determinant of success in ossiculoplasty . Accepted for publication, American Journal of Otolaryngology Head and Neck Medicine and Surgery 2009.
2.        Amit Kochhar, Simon I Angeli, Sandeep Dave,  Xue Z. Liu. Imaging correlation of children with DFNB1 versus non-DFNB1 hearing loss. Otolaryngology Head and Neck Surgery 2009.
3.        Angeli SI. Phenotype/genotype correlations in a DFNB1 cohort with ethnic heterogeneity. Laryngoscope, May 2008.
4.        Xue Z. Liu, Simon I. Angeli, Kaukab Rajput, Denise Yan, Annelle V. Hodges, Adrien Eshraghi, Fred F. Telischi, Thomas J. Balkany. Cochlear implantation in individuals with Usher type 1 syndrome. International Journal of Pediatric Otorhinolaryngology (2008) 72, 841-847.
5.        Christine Dinh, Kimberly Hoang, Scott Haake, Shibing Chen, Simon I. Angeli, Eva Nong, Adrien Eshraghi, Thomas J. Balakny, and Thomas R. Van De Water. Biopolymer-Release Dexamethasone Prevents Tumor Necrosis Facor a Induced Loss of Auditory Hair Cells In Vitro: Implications Toward the Development of a Drug-Eluting Cochlear Implant Electrode Array. Otology & Neurology 2008; 29:1012-1019.
6.        Connell S, Angeli SI, Suarez H, et al. Performance after cochlear implantation in DFNB1 patients.  Otolaryngol Head Neck Surg; 137:596-602 2007
7.        Angeli SI, van de Water T, Connell S, Ozdek, et al. Injectable form of cross-linked hyaluronan is effective for middle ear wound healing.  Annals Otol Rhino Laryngol; 116:667-673 2007
8.        Utreta R, Angeli SI. Detection of the 35delG/GJB2 and del (GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive non-syndromic hearing loss.  Genet Testing May 10, 2007
9.        Yan D, Ouyang XM, Angeli SI, et al.  Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss.  AM J Med Genet Part A 143A:385-386, 2007
10.    Suarez H, Angeli SI, Suarez A.  Balance Sensory Organization in Children with Profound Hearing Loss and Cochlear Implants.  Int J Pediatr Otorhinolaryngol 71: 629-637 2007
11.    Angeli SI, Kulak J, Guzman J. Lateral tympanoplasty for total and near-total perforations: prognostic factors. Laryngoscope 116:1594-1599, 2006.
12.    Ulubil AS, Furze A, Angeli SI. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure. J Laryngol Otol 120:230-2 2006
13.    Simon I. Angeli MD. Hyaluronate gel stapedotomy.  Otolaryngology-Head and Neck Surgery, Volumen 134, No. 3, pp 225-231, 2006
14.    Simon I. Angeli, MD, Denise Yan, PhD, Fred Telischi, MD, Thomas J. Balkany, MD, Xiao M. Ouyang, MD, Li L. Du, MSC, Adrian Eshraghi, MD, Leslie Goodwin, MSN, Xue Z. Liu, MD, PhD. Etiologic diagnosis of sensorineural hearing loss in adults. Otolaryngology-Head and Neck Surgery, Volumen 132, No. 6, pp 888-893, 2005.
15.    Simon I. Angeli, MD, Xue Z. Liu, MD PhD, Denise Yan PhD, Thomas Balkany, MD, Fred Telischi, MD. Coenzyme Q-10 treatment of patients with a 7445A>G mitochondrial DNA mutation stopped the progression of their hearing loss. Acta Oto-Laryngologica;125:1-3 2005
16.    Liu XZ, Pandya A, Angeli SI, Telischi FF, Arnos KS, Nance WE, Balkany T.  Audiological Features of GJB2 (Connexin 26) Deafness.  Ear & Hearing; 26:361-369 2005
17.    Ouyang XM, Yan D, Du LL, Hetjmancik JF, Jacobson SE, Nance WE, Li AR, Angeli SI, Kaiser M, Newton V, Brown SDM, Balkany T, Liu XZ. Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population. Hum Genet;116:292-299 2005
18.    Ouyang XM, Hejtmancik JF, Jacobson SG, Li AR, Du LL, Angeli SI, Kaiser M, Balkany T, Liu XZ. Mutational spectrum in Usher syndrome type II. Clin Genet. 2004 Apr;65(4):288-93. Erratum in: Clin Genet;65(5):433 May 2004.
19.    S Angeli, O Gomez and R Hawley. Systematic approach to BPPV in the elderly. Otolaryngology-Head and Neck Surgery 128:719-25 2003
20.     S Angeli. The value of quantitative vestibular testing in infants and young children with sensorineural hearing loss. Archives of Otolaryngology-Head and Neck Surgery; 129: 478-482 2003
21.    Angeli SI and Balkany TJ. Post-cochlear implant meningitis. Operative Techniques in Otolaryngology-Head and Neck Surgery;14(4):293-296 2003
 
22.    Liu XZ, Xia XJ, Ouyang XM, Ke XM, Wang HL, Angeli S, Du LL, Telischi F, Liu YH, Balkany T, Nance WE, Xu LR. The prevalence of the conexin 26 (GJB2) mutations in the Chinese population. Human Genetics;11:394-7 2002
23.    Angeli SI, A De La Cruz, and Hitselberger T. The transcochlear approach revisited. Otology and Neurotology; 22:690-695 2001
24.    S Angeli, R Utrera, S Dib, E Chiossone, C Naranjo.  GJB2 mutations in childhood deafness. Acta Otolaryngol (Stockh) 120: 133-136 2000
25.   S Angeli, C. Naranjo, R.A. Freidman, A. Naranjo, O. Henriquez, N. Fischel-Ghodsian and E. Chiossone. An analysis of a large postlingually deaf family with hereditary non-syndromic profound Hearing loss. Acta Otolaryngol (Stockh); 119: 158-162 1999