The Influence of Clinical and Environmental Risk Factors in the Etiology of Congenital Sensorineural Hearing Loss in the Romanian Population
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Abstract
Abstracts Abstracts Abstracts
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3. Abdurehim Y, Lehmann A, Zeitouni AG (2017). Predictive value of GJB2 mutation status for hearing outcomes of pediatric cochlear implantation. Otolaryngol Head Neck Surg, 157:16–24.
4. Naseri M, Akbarzadehlaleh M, Masoudi M, et al (2018). Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Au-tosomal Recessive Non-syndromic Hear-ing Loss: Evidence for Digenic Inher-itance in GJB2 and GJB3 Mutations. Iran J Public Health, 47(1): 95-102.
5. Palmer CGS, Lueddeke JT, Zhou J (2009). Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child. Genet Med, 11(4): 248–255.
6. Lazăr C, Popp R, Trifa A, et al (2010). Preva-lence of the c.35delG and pW24X muta-tions in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania. Int J Pediatr Otorhinolaryn-gol, 74(4): 351-355.
7. Totolin M. Modern, clinical, audiological, and ge-netic methods to investigate congenital neurosensory hypocausts [PhD thesis]. Carol Davila Uni-versity of Medicine and Pharmacy, Ro-mania; 2011.
8. Neagu A. Genetic and clinical study in congenital non-syndromic neurosurgery [PhD thesis]. Carol Davila University of Medicine and Pharmacy, Romania; 2013.
2. Bostan I (2016). Investigating the Effective-ness of Programs on Health Financing Based on Audit Procedures. Iran J Public Health, 45(8): 1074-1079.
3. Abdurehim Y, Lehmann A, Zeitouni AG (2017). Predictive value of GJB2 mutation status for hearing outcomes of pediatric cochlear implantation. Otolaryngol Head Neck Surg, 157:16–24.
4. Naseri M, Akbarzadehlaleh M, Masoudi M, et al (2018). Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Au-tosomal Recessive Non-syndromic Hear-ing Loss: Evidence for Digenic Inher-itance in GJB2 and GJB3 Mutations. Iran J Public Health, 47(1): 95-102.
5. Palmer CGS, Lueddeke JT, Zhou J (2009). Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child. Genet Med, 11(4): 248–255.
6. Lazăr C, Popp R, Trifa A, et al (2010). Preva-lence of the c.35delG and pW24X muta-tions in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania. Int J Pediatr Otorhinolaryn-gol, 74(4): 351-355.
7. Totolin M. Modern, clinical, audiological, and ge-netic methods to investigate congenital neurosensory hypocausts [PhD thesis]. Carol Davila Uni-versity of Medicine and Pharmacy, Ro-mania; 2011.
8. Neagu A. Genetic and clinical study in congenital non-syndromic neurosurgery [PhD thesis]. Carol Davila University of Medicine and Pharmacy, Romania; 2013.
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| Issue | Vol 48 No 12 (2019) | |
| Section | Letter to the Editor | |
| DOI | https://doi.org/10.18502/ijph.v48i12.3566 | |
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How to Cite
1.
MOCANU H, ONCIOIU I. The Influence of Clinical and Environmental Risk Factors in the Etiology of Congenital Sensorineural Hearing Loss in the Romanian Population. Iran J Public Health. 2019;48(12):2301-2303.
