Items where Subject is "WV Otolaryngology"

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Number of items at this level: 89.

A

Abbasi, S. and Khaledi, M. and Gholipour, A. and Heydari, R. (2017) Assessment of the Prevalence of Staphylococcus Areus in Nose of the Surgical Staff of Hajar and kashani's Hospital in 2015. Journal of Shahrekord Uuniversity of Medical Sciences, 19.

Abolhassani, M. and Hashemzade Chaleshtori, M. and Iziy, E. and Motovalibashi, M. and Khazraei, H. and Ramazi, Sh. (2015) Association of interleukin-18 gene polymorphism-137 G/C with allergic rhinitis. Journal of Gorgan University of Medical Sciences, 17 (2).

Aein, F. (2003) Effect of distraction and relaxation on pain-intensity during the postoperative 24 hours in children. Journal of Shahrekord Uuniversity of Medical Sciences, 4.

Ahmadi, H. and Daramadi, P.S. and Asadi-Samani, M. and Givtaj, H. and Sani, M.R.M. (2017) Effectiveness of group training of assertiveness on social anxiety among deaf and hard of hearing adolescents. International Tinnitus Journal, 21 (1). pp. 14-20.

Akhlaghi, M. and Abedinzadeh, M. and Ahmadi, A. and Heidari, Z. (2017) Predicting Difficult Laryngoscopy and Intubation With Laryngoscopic Exam Test: A New Method. Acta medica Iranica, 55 (7). pp. 453-458. ISSN 1735-9694

Akhlaghi, M. and Kheiri, S. and Khazraei, H. and Madineh, H. (2006) Comparsion of atracurium and succinylcholine on post adenotonsillectomy pain in children of 3-12 years old. Journal of Shahrekord Uuniversity of Medical Sciences, 8.

Alipour, P. and Tabatabaiefar, M.A. and Reiisi, S. and Fattahi, N. and Pourahmadian, A. and Hashemzadeh-Chaleshtori, M. (2015) Genetic linkage analysis of the DFNB63 locus in families with autosomal recessive nonsyndromic hearing loss from Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran. Journal of Isfahan Medical School, 33 (346). pp. 1308-1317.

Amani, S. and Khazraei, H. (2011) Nasopharyngeal Mixed Tumor: A Case Report. Zahedan Journal of Research in Medical Sciences, 16 (11).

Amani, S. and Khazraie, H.R. (2005) Relationship between serous otitis media and its risk factors in primary school students in Shahrekord. Journal of Shahrekord Uuniversity of Medical Sciences, 7.

Amani, S. and Moeini, M. (2016) Comparison of boric acid and combination drug of polymyxin, neomycin and hydrocortisone (Polymyxin NH) in the treatment of acute otitis externa. Journal of Clinical and Diagnostic Research, 10 (7).

Amani, S. and Rasti Boroujeni, M. and Abedin zade, M.R. (2006) Effects of local injection of bupivacaine and dexamethasone on postoperative pain of adenotonsillectomy. Journal of Shahrekord Uuniversity of Medical Sciences, 8.

Asgharzade, S. and Chaleshtori, M.H. and Tabatabaifar, M.A. and Reisi, S. and Modaressi, M.H. (2016) Mutation in second exon of myo15a gene cause of nonsyndromic hearing loss and its association in the Arab population in Iran. Genetika, 48 (2). pp. 587-596.

B

Banitalebi, G. and Montazerzohor, M. and Farokhi, E. and Abolhasani, M. and Reissi, S. and Heydari, S. and Ataii, Z. and Azadegan-Dehkordi, F. and Hoseinipoor, A. and Hashemzadeh-Chaleshtory, M. (2012) Study of three common mitochondrial mutations in Arab patients with nonsyndromic hearing loss in Khuzestan province, I.R.Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Baradaranfar, M.H. and Dodangeh, F. and Taghipour-Zahir, S. and Atar, M. (2007) Humoral and cellular immunity parameters in children before and after adenotonsillectomy. Acta Medica Iranica, 45 (5). pp. 345-350.

Baradaranfar, M.H. and Labibi, M. (2007) Anatomic variations of paranasal sinuses in patients with chronic sinusitis and their correlation with CT scan staging. Acta Medica Iranica, 45 (6). pp. 477-480.

D

Delphi, M. and Bayati, A. and Delphi, V. and Ryahi, F. (2013) Evaluation of auditory efferent system function in children with autism. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

F

Fatehi, D. and Van Rhoon, G.C. (2008) SAR characteristics of the Sigma-60-Ellipse applicator. INTERNATIONAL JOURNAL OF HYPERTHERMIA, 24 (4). pp. 347-356.

Fattahi, N. and Tabatabaiefar, M.A. and Reeisi, S. and Alipour, P. and Pourahmadian, A. and Hashemzadeh Chaleshtory, M. (2015) Genetic linkage analysis of DFNB59 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in western provinces of Iran. journal of shahrekord university of medical sciences, 17 (4).

G

Ghorbani, R. and Sadolahi, A. and Mohamadi, O. (2011) Effects of smoking cigarette on some acoustic voice parameters and elements of speech pattern of male subjects. Koomesh, 12 (3).

Ghorbani, R. and Sadolahi, A. and Mohamadi, O. (2010) The effect of hearing loss on acoustic parameters of voice in children. Medical Journal of Mashhad University of Medical Sciences, 53 (3).

H

Hamidi, M. and Karimipoor, M. and Hashemzadeh Chaleshtori, M. and Akbari, M.T. (2009) A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients. JOURNAL OF GENETICS, 88 (3). pp. 359-362.

Hashemzadeh Chaleshtori, M. and Farhud, D.D. and Crosby, A.H. and Farrokhi, E. and Jafari Pour, H. and Ghatreh Samani, K. and Safa Chaleshtori, K. and Kasiri, M. and Shahrani, M. and Mobini, G.R. and Banitalebi, M. and Mansouri, M. and Modarresinia, D. and Jafari, M. (2008) Molecular pathology of 6 novel GJB2 allelic variants detected in familial and sporadic Iranian non syndromic hearing loss cases. IRANIAN JOURNAL OF PUBLIC HEALTH, 37 (3). pp. 9-18.

Hashemzadeh Chaleshtori, M. and Farhud, D.D. and Patton, M.A. (2007) Familial and sporadic GJB2-related deafness in iran: Review of gene mutations. IRANIAN JOURNAL OF PUBLIC HEALTH, 36 (1). pp. 1-14.

Hashemzadeh Chaleshtori, M. and Farrokhi, E. and Shahrani, M. and Kheiri, S. and Dolati, M. and Hoghooghi Rad, L. and Pour-Jafari, H. and Ghatreh Samani, K. and Safa Chaleshtori, K. and Crosby, A.H. (2007) High carrier frequency of the GJB2 mutation (35delG) in the north of Iran. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 71 (6). pp. 863-867.

Hashemzadeh Chaleshtori, M. and Montazer Zohour, M. and Hoghooghi Rad, L. and Pour-Jafari, H. and Farhud, D.D. and Dolati, M. and Safa Chaleshtori, K. and Sasanfar, R. and Hosseinipour, A. and Andonian, L. and Tolouei, A. and Ghadami, M. and Patton, M.A. (2006) Autosomal recessive and sporadic non syndromic hearing loss and the incidence of Cx26 mutations in a province of Iran. Iranian Journal of Public Health, 35 (1). pp. 88-91.

Hashemzadeh Chaleshtori, M. and Simpson, M.A. and Farrokhi, E. and Dolati, M. and Hoghooghi Rad, L. and Amani Geshnigani, S. and Crosby, A.H. (2007) Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. CLINICAL GENETICS, 72 (3). pp. 261-263.

Hashmzade Chaleshtori, M. and Akbari, M.T. and Khazraei, H. and Abolhasani, M. and Reisi, S. and Ataei, Z. and Saedi-Marghmaleki, M. and Shirmardi, S.A. and Farrokhi,, E. and Montazer-Zohouri, M. and Azadegan-Dehkordi, F. (2011) Screening of three common mtDNA mutations among subjects with autosomal recessive non-syndromic hearing loss in Sistan va Baluchestan province, Iran. Zahedan Journal of Research in Medical Sciences, 13 (5).

Hemati, Z. and Abbasi, S. and Paki, S. and Kiani, D. (2017) The Effect of Happiness Training Based on Fordyce Model on Perceived Stress in the Mothers of Children with Cleft Lip and Palate. Journal of caring sciences, 6 (2). pp. 173-181. ISSN 2251-9920

Hemati, Z. and Derakhshande, F. and Abbasi, S. and Kiani, D. (2017) The effect of happiness training on self-esteem in the mothers of children with cleft lip and palate in Isfahan 2015. Journal of education and health promotion, 6. p. 68. ISSN 2277-9531

Hosseinipour, A. and Chaleshtori, M.H. and Sasanfar, R. and Farhud, D.D. and Tolooi, A. and Doulati, M. and Rad, L.H. and Montazer Zohour, M. and Ghadami, M. (2005) Report of a new mutation and frequency of connexin 26 gene (GJB2) mutations in patients from three provinces of Iran. Iranian Journal of Public Health, 34 (1). pp. 47-50.

I

Iranmanesh, S. and Rafiei, H. and Esmaeili Abdar, M. (2012) Letter: A case of pressure ulcer development on a patient's ear as a result of pulse oximetry probe. International Wound Journal, 9 (6). pp. 701-702.

K

Karami-Eshkaftaki, R. and Ahmadinejad, F. and Aghaei, Sh. and Moghim, H. and Hashemzadeh-Chaleshtori, M. and Jami, M. (2017) Hearing loss: A review on molecular genetics and epidemiologic aspects. International Journal of Epidemiologic Research, 4 (2). pp. 166-172.

Kargoshaie, A.A. and Akhlaghi, M. and Najafi, M. (2009) Oxygen saturation improvement after adenotonsillectomy in children. Pakistan journal of biological sciences : PJBS, 12 (3). pp. 276-80. ISSN 1028-8880

Kargoshaie, A.A. and Najafi, M. and Akhlaghi, M. and Khazraie, H.R. and Hekmatdoost, A. (2009) The correlation between tonsil size and academic performance is not a direct one, but the results of various factors. ACTA OTORHINOLARYNGOLOGICA ITALICA, 29 (5). pp. 255-258.

Khazraei, H. and Amani, S. (2006) Comparison of the effect of amoxicillin and cefriaxone in treatment of acute otitis media in children under 6 years old. Journal of Shahrekord Uuniversity of Medical Sciences, 7.

Khodami, A. and Shahtoosi, M. and Amani, S. and Khazraei, H. (2015) The Comparison of Ginkgo biloba and Cinnarizine effectiveness in tinnitus intensity of patients with subjective tinnitus. Journal of Birjand University of Medical Sciences, 21 (4).

Khoshdel, A. and Panahande, G.R. and Noorbakhsh, M.K. and Ahmadi, M.R.M. and Lotfizadeh, M. and Parvin, N. (2014) A comparison of the efficacy of amoxicillin and nasal irrigation in treatment of acute sinusitis in children. Korean Journal of Pediatrics, 57 (11). pp. 479-483.

Kooshavar, D. and Tabatabaiefar, M.A. and Farrokhi, E. and Abolhasani, M. and Noori-Daloii, M.R. and Hashemzadeh Chaleshtori, M. (2013) Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 77 (2). pp. 189-193.

M

Madineh, H. and Khazraei, H. and Kheiri, S. and Akhlaghi, M. (2006) Comparsion of atracurium and succinylcholine on post adenotonsillectomy pain in children of 3-12 years old. Journal of Shahrekord Uuniversity of Medical Sciences, 8.

Mahmoudian Sani, M. and Mehri-Ghahfarrokhi, A. and Ahmadi, H. and Shojaeian, A. and Hashemzadeh-Chaleshtori, M. and Mahdavinezhad, A. and Saidijam, M. (2017) Study of common mitochondrial mutations in patients with nonsyndromic hearing loss. Otorinolaringologia, 67 (2). pp. 61-67.

Mahmoudian-Sani, M.R. and Hashemzadeh-Chaleshtori, M. and Asadi-Samani, M. and Luther, T. (2017) A review of medicinal plants for the treatment of earache and tinnitus in Iran. International Tinnitus Journal, 21 (1). pp. 44-49.

Mahmoudian-Sani, M.R. and Hashemzadeh-Chaleshtori, M. and Asadi-Samani, M. and Yang, Q. (2017) Ginkgo Biloba in the treatment of tinnitus: An updated literature review. International Tinnitus Journal, 21 (1). pp. 58-62.

Mahmoudian-sani, M.-R. and Mehri-Ghahfarrokhi, A. and Ahmadinejad, F. and Hashemzadeh-Chaleshtori, M. and Saidijam, M. and Jami, M.-S. (2017) MicroRNAs: effective elements in ear-related diseases and hearing loss. European Archives of Oto-Rhino-Laryngology. pp. 1-8.

Mahmoudian-sani, M.-R. and Mehri-Ghahfarrokhi, A. and Ahmadinejad, F. and Hashemzadeh-Chaleshtori, M. and Saidijam, M. and Jami, M.-S. (2017) MicroRNAs: effective elements in ear-related diseases and hearing loss. European Archives of Oto-Rhino-Laryngology, 274 (6). pp. 2373-2380.

Mehri-Ghahfarrokhi, A. and Hashemzadeh-Chaleshtori, M. and Shojaeian, A. and Mahmoudian-Sani, M.R. (2017) Studying gap junction beta 2-related deafness in Iranian population. Otorinolaringologia, 67 (3). pp. 89-95.

Moghim, H. and Ganji, F. and Khalili, B. and Khazraei, H. (2013) Prevalence of fungi in patients with allergic rhinitis in Shahrekord, Iran (2009). Journal of Gorgan University of Medical Sciences, 15 (1).

Mohamadi, O. and Pourgharib, J. (2008) Persian vowels formants; an investigation and comparison between Persian children 7-9 years old and Persian adults 18-22 years old. Koomesh, 9 (2).

Mojtabavi Naeini, M. and Vallian, S. and Hashmzadeh Chaleshtori, M. (2014) Investigation of D7S496 marker characteristics in five Iranian ethnic groups for linkage analysis of autosomal recessive non syndromic hearing loss. journal of shahrekord university of medical sciences, 15 (6).

Montazer Zohour, M. and Tabatabaiefar, M.A. and Azadegan Dehkordi, F. and Farrokhi, E. and Akbari, M.T. and Hashemzade Chaleshtori, M. (2012) Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment. GENETIC TESTING AND MOLECULAR BIOMARKERS, 16 (4). pp. 271-278.

Montazer- Zohour, M. and Hashemzadeh-Chaleshtori, M. and Akbari, M. T. (2012) Frequency of the common mitochondrial DNA (mtDNA) mutations in non-syndromic hearing impairment in southwest subpopulations of Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Moradipour, N. and Ghasemi-Dehkordi, P. and Heibati, F. and Parchami-Barjui, S. and Abolhasani, M. and Rashki, A. and Hashemzadeh-Chaleshtori, M. (2016) Mutation screening of exons 7 and 13 of the TMC1 gene in autosomal recessive non-syndromic hearing loss (ARNSHL) in Iran. Iranian Red Crescent Medical Journal, 18 (2).

Mortazavi, M. and Shareghi, A. and Ghiassi-Nejad, M. and Kavousi, A and Jafari Zadeh, M. and Nazeri, F. and Mozdarani, H. (2004) The need for national diagnostic reference levels: Entrance surface dose measurement in intraoral radiography. Iran. J. Radiat. Res, 2 (3).

Motamedi, S. and Hashemzadeh-Chaleshtori, M. and Mojtabavi-Naeini, M. and Teimori, H. (2015) Genetic variation of D9S1837 Marker located at TMC1 gene in Iranian population. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

N

Naeini, M.M. and Boroujeni, S.V. and Chaleshtori, M.H. (2014) Population data on d7s2425 marker in five ethnic groups of the iranian population: A highly informative marker for molecular diagnosis of ARNSHL. Journal of Kerman University of Medical Sciences, 21 (6). pp. 540-550.

Nasimi, A. and Rees, A. (2000) Temporal pattern of neuronal responses (PSTH) to pure tone in the inferior Colliculus. Journal of Shahrekord Uuniversity of Medical Sciences, 2.

O

Okhovat, A.R. and Mirmohammad Sadeghi, M. and Roghani, M. (2005) The effect of lidocaine spray early after tonsillectomy on pain and vomiting. Journal of Shahrekord Uuniversity of Medical Sciences, 7.

P

Parchami-Barjui, S. and Reiisi, S. and Rezaiean, F. and Heybati, F. and Hashemzadeh-Chaleshtori, M. (2014) Screening LRTOMT gene (DFNB63 locus) in patients with recessive nonsyndromic hearing loss in hormozgan province, Iran. Journal of Isfahan Medical School, 32 (298). pp. 1330-1337.

Parvin, N. and Shahinfard, N. and Farrokhi, E. and Kasiri, M. and Khoshdel, A. and Amani, S. and Hoseynzadeh, Sh. and Shirmardi, A. and Noeparast, Z. and HashemzadehChaleshtori, M. (2009) The frequenc of hearing loss etiology among deaf students in Chaharmahal va Bakhtiari province Iran 2008-2009. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

Pourahmadiyam, A. and Tabatabaefar, M.A. and Reiisi, S. and Alipour, P. and Fattahi, N. and Hashemzadeh Chaleshtori, M. (2016) Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province. journal of shahrekord university of medical sciences, 18 (3).

Pourahmadiyan, A. and Tabatabaiefar, M.A. and Reiisi, S. and Alipour, P. and Fattahi, N. and Hashemzadeh-Chaleshtori, M. (2016) Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran. Journal of Isfahan Medical School, 34 (374).

R

Ramazi, Sh. and Motovalibashi, M. and Hashemzade-Chaleshtori, M. and Khazraei, H. (2014) Introduction of Interleukin-18 genotype as a risk factor for allergic rhinitis in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Reiisi, S. and Sanati, M.H. and Tabatabaiefar, M.A. and Ahmadian, Sh. and Reiisi, S. and Parchami-Barjui, Sh. and Porjafari, H. and Shahi, H. and Shavarzi, A. and Hashemzade Chaleshtori, M. (2014) The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations. International journal of molecular and cellular medicine, 3 (3). pp. 176-82. ISSN 2251-9637

Reiisi, S. and Sanati, M.H. and Tabatabaiefar, M.A. and Pourjafari, H.R. and Minuchehr, Z. and Shavarzi, A. and Ataie, M. and Kasiri, M. and Hashemzadeh-Chaleshtori, M. (2014) Study of the association of DFNB3 locus with autosomal recessive non-syndromic hearing loss in iranian deaf population using genetic linkage analysis. Journal of Isfahan Medical School, 32 (285). pp. 669-677.

Reiisi, S. and Tabatabaiefar, M.A. and Sanati, M.H. and Chaleshtori, M.H. (2016) Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family. Iranian Journal of Basic Medical Sciences, 19 (7). pp. 772-778.

Reissi, N. and Kargoshaie, A.A. (2004) Prevalence of hearing loss in patients with Beta thalassemia major, Hajar hospital of Shahrekord, 2002. Journal of Shahrekord Uuniversity of Medical Sciences, 6.

Rezaeian, F. and Tabatabaiefar, M.A. and Heybati, F. and Reiisi, S. and Parchami, Sh. and Abolhasani, M. and Amiri, B. and Salehi, A.R. and Hashemzadeh-Chaleshtori, M. (2014) Genetic linkage analysis of DFNB93 locus in a group of families with autosomal recessive non-syndromic hearing loss in Chahar Mahal & Bakhtiari and Kohkiluyeh & Boyer Ahmad provinces of Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Rouzbahani, H. and Badiee, P. and Barkhordar, M. and Rabiee, A. and Faramarzi, A. and Rouzbahani, R. and Moghadami, M. (2011) Etiologic Causes of Invasive Fungal Sinusitis among Patients of, University Hospitals in Shiraz, Iran. Journal of Isfahan Medical School, 29 (153).

S

Sadeghi, A. and Sanati, M.H. and Alasti, F. and Chaleshtori, M.H. and Mahmoudian, S. and Ataei, M. (2009) Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran. Iranian Journal of Biotechnology, 7 (2). 108-111+120.

Sadeghi, M. and Kheyri, S. and Jafari dastenai, A. and Shahrani, M. (2007) Sound level in a ten year period in Shahrekord City. Journal of Shahrekord Uuniversity of Medical Sciences, 8.

Sadeghian, Ladan and Tabatabaiefar, Mohammad Amin and Zarepour, Narges and Hashemzadeh-chaleshtori, Morteza (2017) Genetic linkage analysis of DFNB24 locus in a group of families with autosomal recessive non-syndromic hearing loss in Khouzestan province of Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 19.

Safavi, M.R. and onarmand, A. (2008) Prediction of difficult laryngoscopy in the patients undergone cesarean section. Journal of Shahrekord Uuniversity of Medical Sciences, 9.

Salehi Chaleshtori, A.R. and Tabatabaiefar, M.A. and Salehi, H.R. and Chaleshtori, M.H. (2014) Analysis of CABP2 c.637+1G>T mutation in iranian patients with non-syndromic sporadic hearing loss. Genetics in the Third Millennium, 12 (2). pp. 3504-3511.

Sani, M.R.M. and Hashemzadeh-Chaleshtori, M. and Mehri-Ghahfarrokhi, A. and Ghasemi-Dehkordi, P. and Saidijam, M. and Jami, M.-S. (2016) MicroRNA-183 family in inner ear: Hair cell development and deafness. Journal of audiology and otology, 20 (3). pp. 131-138.

Sasanfar, R. and Tolouei, A. and Hoseinipour, A. and Farhud, D. and Dolati, M. and Rad, L. and Zohour, M. and Ghadami, M. and Pour-Jafari, H. and Chaleshtori, M. (2004) Frequency of a very rare 35delG mutation in two ethnic groups of Iranian populations. Iranian Journal of Public Health, 33 (4). pp. 26-30.

Schrauwen, I. and Helfmann, S. and Inagaki, A. and Predoehl, F. and Tabatabaiefar, M.A. and Picher, M.M. and Sommen, M. and Seco, C.Z. and Oostrik, J. and Kremer, H. and Dheedene, A. and Claes, Ch. and Fransen, E. and Hashemzadeh Chaleshtori, M. and Coucke, P. and Lee, A. and Moser, T. and Van Camp, G. (2012) A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. AMERICAN JOURNAL OF HUMAN GENETICS, 91 (4). pp. 636-645.

Sedehi, M. and Rahimi-Madiseh, M. and Mohamadi, O. (2016) The prevalence of stuttering, voice disorder and speech sound disorders in preschoolers in Shahrkord, Iran. Intenational Journal of child, youth and family studies, 7 (3/4).

T

Tabatabaiefar, M.A. and Alasti, F. and Montazer Zohour, M. and Shariati, L. and Farrokhi, E. and Farhud, D.D. and Camp, G.V. and Noori-Daloii, M.R. and Hashemzadeh Chaleshtori, M. (2011) Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss. IRANIAN JOURNAL OF PUBLIC HEALTH, 40 (2). pp. 34-48.

Tabatabaiefar, M.A. and Alasti, F. and Shariati, L. and Farrokhi, E. and Fransen, E. and Nooridaloii, M.R. and Chaleshtori, M.H. and Van Camp, G. (2011) DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment. CLINICAL GENETICS, 79 (6). pp. 594-598.

Taghipour-Sheshdeh, A. and Tabatabaiefar, M.A. and Nemati-Zargaran, F. and Moradi, F. and Zarepour, N. and Hashemzadeh Chaleshtori, M. (2016) Genetic linkage analysis of the DFNB48 and DFNB98 loci in families with Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) from Khouzestan province. journal of shahrekord university of medical sciences, 18 (6).

Taghizadeh, S.H. and Kazeminezhad, S.R. and Sefidgar, S.A.A. and Yazdanpanahi, N. and Tabatabaeifar, M.A. and Yousefi, A. and Lesani, S.M. and Abolhasani, M. and Hashemzadeh Chaleshtori, M. (2013) Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss. International journal of molecular and cellular medicine, 2 (1). pp. 41-5. ISSN 2251-9637

Tahmasebian, Sh. and Habibi Gahfarokhi, H. and Safdari, R. and Danesh Shahraki, A. (2015) The Usage of Association Rule Mining to Identify Influencing Factors on Deafness After Birth. Acta Informatica Medica, 23 (6).

TahrzadehGharofi, M. and Farkhoi, E. and Shirmardi, S.A. and Safari Chaleshtori, J. and Asadi, S. and Ghatreh Samani, K. and Abolhasani, M. and HajiHoseyni, R. and HashemzadehChaleshtori, M. (2010) DFNB59 gene mutations screening in non syndromic deaf subjects in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

V

Vanwesemael, M. and Schrauwen, I. and Ceuppens, R. and Alasti, F. and Jorssen, E. and Farrokhi, E. and Chaleshtori, M.H. and Van Camp, G. (2011) A 1bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame. American Journal of Medical Genetics, Part A, 155 (8). pp. 2021-2023.

Vatankhah, V. and Khazraei, H. and Iranpoor, H. and Lotfizadeh, M. (2017) Impact of high body mass index on allergic rhinitis patients. Revue Francaise d'Allergologie.

Vatankhah, V. and Lotfizadeh, M. and Iranpoor, H. and Jafari, F. and Khazraei, H. (2016) Comparison vitamin D serum levels in allergic rhinitis patients with normal population. Revue Francaise d'Allergologie, 56 (7-8). pp. 539-543.

Y

Yazdanpanahi, N. and Hashemzadeh Chaleshtori, M. and Tabatabaiefar, M.A. and Noormohammadi, Z. and Farrokhi, E. and Najmabadi, H. and Shahbazi, Sh. and Hosseinipour, A. (2012) Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 76 (6). pp. 845-850.

Yazdanpanahi, N. and Tabatabaiefar, M.A. and Bagheri, N. and Azadegan Dehkordi, F. and Farrokhi, E. and Hashemzadeh Chaleshtori, M. (2015) The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness. INTERNATIONAL JOURNAL OF AUDIOLOGY, 54 (2). pp. 124-130.

Yazdanpanahi, N. and Tabatabaiefar, M.A. and Farrokhi, E. and Abdian, N. and Bagheri, N. and Shahbazi, Sh. and Noormohammadi, Z. and Hashennzadeh Chaleshtori, M. (2013) Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome. CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY, 6 (4). pp. 201-208.

Z

Zohour, M.M. and Akbari, M.T. and Chaleshtori, M.H. (2012) Frequency of the mitochondrial A1555G mutation in Iranian patients with non-syndromic hearing impairment. Indian Journal of Science and Technology, 5 (10). pp. 3378-3383.

This list was generated on Mon Sep 25 01:01:04 2017 IRST.