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Abbasi, Safieh. and Khaledi, Mansoor. and Gholipour, Abolfazl. and Heydari, Reza. (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.
Abedinzadeh, Mohammadreza. and Amani, Soroush. (2015) Effects of Oral Gabapentin, Local Bupivacaine and Intravenous Pethidine on Post Tonsillectomy Pain. Iranian journal of otorhinolaryngology, 27 (82).
Abolhassani, Marziyeh. and Hashemzade Chaleshtori, Morteza. and Iziy, Elham. and Motovalibashi, Majid. and khazraei, Hamid reza. and Ramazi, Shahin. (2015) Association of interleukin-18 gene polymorphism-137 G/C with allergic rhinitis. Journal of Gorgan University of Medical Sciences, 17 (2).
Aein, Fereshteh (2003) Effect of distraction and relaxation on pain-intensity during the postoperative 24 hours in children. Journal of Shahrekord Uuniversity of Medical Sciences, 4.
Afzali, Sayed Lotfollah and Panahi, Hesam and Ganji, Forouzan and Ziaei, Sanaz and Sedaghat, Nahad (2021) Re-Evaluating the Effect of Preoperative Tranexamic Acid on Blood Loss and Field Quality During Rhinoplasty: A Randomized Double-Blinded Controlled Trial. AESTHETIC PLASTIC SURGERY.
Ahmadi, Ali. and Mohammadi-Najafabadi, Ali. and Amani, Soroush. (2016) Comparison of Efficacy and Side Effects of Azithromycin and Co-Amoxiclav in the Treatment of Acute Sinusitis in Adults: A Randomized Clinical Trial. Global journal of health science, 8 (11).
Ahmadi, Hamed. and Sharifi Daramadi, Parviz. and Asadi-Samani, Majid. and Givtaj, Hamed. and Mahmoudian Sani, Mohammad Reza. (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, Mahmood. and Abedinzadeh, Mohammadreza. and Ahmadi, Ali. and Heidari, Zohre. (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, Mahmood. and Kheiri, Soleiman. and khazraei, Hamid reza. and Madineh, Hossein. (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.
Aleebrahim-Dehkordy, E and Ansaripour, S and Rafieian-Kopaei, M and Saberianpour, S (2018) Effects of substances on plants' active compounds on changes in the hormone levels of the pituitary-thyroid axis in hyperthyroidism and hypothyroidism. Pharmacognosy Reviews, 12 (23).
Alipour, Paria. and Tabatabaiefar, Mohammad Amin. and Reiisi, Somayeh. and Fattahi, Najmeh. and Pourahmadian, Azam. and Hashemzadeh-Chaleshtori, Morteza. (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, Soroush. and Khazraie, Hamidreza. (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, Soroush. and Moeini, Mohammad. (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, Soroush. and Rasti Boroujeni, Maryam. and Abedin zade, MohammadReza. (2006) Effects of local injection of bupivacaine and dexamethasone on postoperative pain of adenotonsillectomy. Journal of Shahrekord Uuniversity of Medical Sciences, 8.
Amani, Soroush. and Shabanian, Gholamreza. (2013) Effect of Coriandrum sativum seed extract on the signs of allergic rhinitis. Feyz, Journal of Kashan University of Medical Sciences, 17 (4).
Amani, Soroush. and khazraei, Hamid reza. (2011) Nasopharyngeal Mixed Tumor: A Case Report. Zahedan Journal of Research in Medical Sciences, 16 (11).
Amiri-Andy, Safar-Ali and Sarokhani, Diana and Azami, Milad and Vazini, Hossein and Rezaei-Tavirani, Mostafa and Hasanpour Dehkordi, Ali (2018) Systematic Review and Meta-analysis of Otitis Media in Iran: Prevalence, Etiology, Antibiotic Susceptibility, and Complications. INDIAN JOURNAL OF OTOLOGY, 24 (1).
Arbabi, Mohsen and Sadeghi, Mehraban and Fadaei, Abdolmajid and Hemati, Sara and Shahsavan, S (2018) Evaluation of sulfadiazine(Sdz) removal from wastewater by persulfate activated with iron sulfate. Desalination and Water Treatment, 113.
Asadpour, Nabiallah and Amani, Soroush and Malekpour Tehrani, Afsaneh and Azizian, Sahar (2021) Frequency determination association of parent's smoking with tonsillectomy in children referring to Kashani hospital in Shahrekord in 2017-2018. Jundishapur Scientific Medical Journal, 20 (1). pp. 11-19.
Asgharzadeh, Samira. and Hashemzadeh-Chaleshtori, Morteza. and Tabatabaiefar, Mohammad Amin. and Reisi, Somayeh and Modarressi, Mohammad Hossein. (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.
Asgharzadeh, Samira. and Tabatabaiefar, Mohammad Amin. and Mohammadi-Asl, Javad. and Hashemzadeh Chaleshtori, Morteza. (2018) A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing. International Journal of Pediatric Otorhinolaryngology, 108.
Askari, Masomeh and Moradi, Zahra and Mohammadi, Mahsa and Lagzian, Milad and Asgharzade, Samira (2021) Prediction and interpretation of rare missense variant in OTOG associated with hearing loss. GENOMICS, 113 (4). pp. 2793-2799. ISSN 0888-7543
Azadegan-Dehkordi, F and Ahmadi, R and Bahrami, T and Yazdanpanahi, N and Farrokhi, E and Tabatabaiefar, MA and Hashemzadeh-Chaleshtori, mahmoud (2018) A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss. Am J Otolaryngol.
Azadegan-Dehkordi, F and Ahmadi, R and Koohiyan, M and Hashemzadeh-Chaleshtori, M (2018) Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss. Ann Hum Genet.
Azadegan-Dehkordi, Fatemeh and Ahmadi, Reza and Koohiyan, Mahbobeh and Hashemzadeh-Chaleshtori, Morteza (2019) Update of spectrum c.35delG and c.-23+1G>A mutations on theGJB2gene in individuals with autosomal recessive nonsyndromic hearing loss. Annals of Human Genetics, 83 (1). pp. 1-10. ISSN 00034800
Azadegan-Dehkordi, Fatemeh and Ashrafi, Korosh and Mobini, Gholam Reza and Yazdanpanahi, Nasrin and Shirzad, Maryam and Farrokhi, Effat and Hashemzadeh-Chaleshtori, Morteza (2021) Detection of two pathogenesis previously unreported myosin xva pathogenic variants in two large Iranian pedigrees with autosomal recessive nonsyndromic hearing loss. INDIAN JOURNAL OF OTOLOGY, 27 (1). pp. 14-21.
Azadegan-Dehkordi, Fatemeh and Koohiyan, Mahbobeh and Hoseini, Masih (2022) An update on autosomal recessive hearing loss and loci involved in it. Indian Journal of Otology, 28 (1). p. 6. ISSN 0971-7749
Azadegan-Dehkordi, Fatemeh and Koohiyan, Mahbobeh and Shirzad, Maryam and Bahrami, Tayyeb and Yazdanpanahi, Nasrin and Tabatabaiefar, MohammadAmin and Pourpaknia, Reza and Farrokhi, Effat and Hashemzadeh-Chaleshtori, Morteza (2019) Mutation analysis of GJB2 and GJB6 genes and screening of nine common dfnb loci in iranian pedigrees with autosomal recessive nonsyndromic hearing loss. Indian Journal of Otology, 25 (2). p. 97. ISSN 0971-7749
Azadegan-Dehkordi, Fatemeh. and Farrokhi, Effat. and Montazer Zohouri, Mostafa. and Mobini, Gholam Reza. and Taherzadeh Ghahfarrokhi, Maryam. and Raiesi, Marzieh. and Raiesi, Somayeh. and Banitalebi, Mehdi. and Hashemzadeh-Chaleshtori, Morteza. and Soleimani, Mahshid. and kasiri, mahboobeh. and Shirmardi, Seyed Abolfath. and Taji, Fatemeh. and Asgari, Azam. and Banitalebi, Golandam. and safari, javad. (2010) DFNB59 Gene Mutation Screening Using PCR-SSCP/HA Technique in Non-syndromic Genetic Hearing Loss in Bushehr Province. ISMJ, 13 (3).
Banitalebi, Golandam. and Montazerzohor, Mostafa. and Farrokhi, Effat. and Abolhasani, Marzieh. and Reissi, Somayeh. and Heydari, Soraya. and Ataii, Zohreh. and Azadegan-Dehkordi, Fatemeh. and Hoseinipoor, Azam. and Hashemzadeh-Chaleshtori, Morteza. (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, Mohammad Hossein. and Dodangeh, Fatemeh. and Taghipour-Zahir, Shokouh. and Atar, Muge. (2007) Humoral and cellular immunity parameters in children before and after adenotonsillectomy. Acta Medica Iranica, 45 (5). pp. 345-350.
Baradaranfar, Mohammad Hossein. 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.
Dehgan, A. (2009) Analysis of acoustic parameters in normal adults who speak Farsi at Zahedan City. journal of shahrekord university of medical sciences, 11 (2).
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.
Fadaei, Reza and Safari-Faramani, Roya and Rezaei, Mohammad and Ahmadi, Reza and Rostampour, Masoumeh and Moradi, Nariman and Khazaie, Habibolah (2020) Circulating levels of oxidized low-density lipoprotein in patients with obstructive sleep apnea: a systematic review and meta-analysis. Sleep and Breathing. ISSN 15209512
Farrokhi, Effat. and Shirmardi, Abolfath. and Khoshdel, Abolfazl. and Amani, Soroush. and Soleimani, Mahshid. and kasiri, mahboobeh. and Rahbarian, Jahanbakhsh. and Parvin, Neda. and Shahinfard, Najmeh. and Hashemzadeh-Chaleshtori, Morteza. (2009) Genetic study of 45 big hearing loss pedigrees and GJB2 gene mutations frequency in Chaharmahal va Bakhtiari province, Iran, 2008. journal of shahrekord university of medical sciences, 10 (4).
Fatehi, Daryoush. and Van Rhoon, Gerard.C. (2008) SAR characteristics of the Sigma-60-Ellipse applicator. INTERNATIONAL JOURNAL OF HYPERTHERMIA, 24 (4). pp. 347-356.
Fattahi, Najmeh. and Tabatabaiefar, Mohammad Amin. and Reeisi, Somayeh. and Alipour, Paria. and Pourahmadian, Azam. and Hashemzadeh-Chaleshtori, Morteza. (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).
Forouzanfar, Fatemeh and Asgharzade, Samira (2020) MicroRNAs in Noise-Induced Hearing Loss and their Regulation by Oxidative Stress and Inflammation. Current Drug Targets, 21. ISSN 13894501
Ghorbani, Raheb. and Sadollahi, Ali. and Mohamadi, Omid. (2011) Effects of smoking cigarette on some acoustic voice parameters and elements of speech pattern of male subjects. Koomesh, 12 (3).
Ghorbani, Raheb. and Sadollahi, Ali. and Mohamadi, Omid. (2010) The effect of hearing loss on acoustic parameters of voice in children. Medical Journal of Mashhad University of Medical Sciences, 53 (3).
Haile, L.M. and Kamenov, K. and Briant, P.S. and Orji, A.U. and Steinmetz, J.D. and Abdoli, A. and Abdollahi, M. and Abu-Gharbieh, E. and Afshin, A. and Ahmed, H. and Rashid, T.A. and Akalu, Y. and Alahdab, F. and Alanezi, F.M. and Alanzi, T.M. and Al Hamad, H. and Ali, L. and Alipour, V. and Al-Raddadi, R.M. and Amu, H. and Arabloo, J. and Arab-Zozani, M. and Arulappan, J. and Ashbaugh, C. and Atnafu, D.D. and Babar, Z.-U.-D. and Baig, A.A. and Banik, P.C. and Bärnighausen, T.W. and Barrow, A. and Bender, R.G. and Bhagavathula, A.S. and Bhardwaj, N. and Bhardwaj, P. and Bibi, S. and Bijani, A. and Burkart, K. and Cederroth, C.R. and Charan, J. and Choudhari, S.G. and Chu, D.-T. and Couto, R.A.S. and Dagnew, A.B. and Dagnew, B. and Dahlawi, S.M.A. and Dai, X. and Dandona, L. and Dandona, R. and Desalew, A. and Dhamnetiya, D. and Dhimal, M.L. and Dhimal, M. and Doyle, K.E. and Duncan, B.B. and Ekholuenetale, M. and Filip, I. and Fischer, F. and Franklin, R.C. and Gaidhane, A.M. and Gaidhane, S. and Gallus, S. and Ghamari, F. and Ghashghaee, A. and Ghozali, G. and Gilani, S.A. and Gl�van, I.-R. and Golechha, M. and Goulart, B.N.G. and Gupta, V.B. and Gupta, V.K. and Hamidi, S. and Hammond, B.R. and Hay, S.I. and Hayat, K. and Heidari, G. and Hoffman, H.J. and Hopf, K.P. and Hosseinzadeh, M. and Househ, M. and Hussain, R. and Hwang, B.-F. and Iavicoli, I. and Ibitoye, S.E. and Ilesanmi, O.S. and Irvani, S.S.N. and Islam, S.M.S. and Iwagami, M. and Jacob, L. and Jayapal, S.K. and Jha, R.P. and Jonas, J.B. and Kalhor, R. and Al-Salihi, N.K. and Kandel, H. and Kasa, A.S. and Kayode, G.A. and Khalilov, R. and Khan, E.A. and Khatib, M.N. and Kosen, S. and Koyanagi, A. and Kumar, G.A. and Landires, I. and Lasrado, S. and Lim, S.S. and Liu, X. and Lobo, S.W. and Lugo, A. and Makki, A. and Mendoza, W. and Mersha, A.G. and Mihretie, K.M. and Miller, T.R. and Misra, S. and Mohamed, T.A. and Mohammadi, M. and Mohammadian-Hafshejani, A. and Mohammed, A. and Mokdad, A.H. and Moni, M.A. and Kandel, S.N. and Nguyen, H.L.T. and Nixon, M.R. and Noubiap, J.J. and Nuñez-Samudio, V. and Oancea, B. and Oguoma, V.M. and Olagunju, A.T. and Olusanya, B.O. and Olusanya, J.O. and Orru, H. and Owolabi, M.O. and Padubidri, J.R. and Pakshir, K. and Pardhan, S. and Kan, F.P. and Pasovic, M. and Pawar, S. and Pham, H.Q. and Pinheiro, M. and Pourshams, A. and Rabiee, N. and Rabiee, M. and Radfar, A. and Rahim, F. and Rahimi-Movaghar, V. and Ur Rahman, M.H. and Rahman, M. and Rahmani, A.M. and Rana, J. and Rao, C.R. and Rao, S.J. and Rashedi, V. and Rawaf, D.L. and Rawaf, S. and Renzaho, A.M.N. and Rezapour, A. and Ripon, R.K. and Rodrigues, V. and Rustagi, N. and Saeed, U. and Sahebkar, A. and Samy, A.M. and Santric-Milicevic, M.M. and Sathian, B. and Satpathy, M. and Sawhney, M. and Schlee, W. and Schmidt, M.I. and Seylani, A. and Shaikh, M.A. and Shannawaz, M. and Shiferaw, W.S. and Siabani, S. and Singal, A. and Singh, J.A. and Singh, J.K. and Singhal, D. and Skryabin, V.Y. and Skryabina, A.A. and Sotoudeh, H. and Spurlock, E.E. and Taddele, B.W. and Tamiru, A.T. and Tareque, M.I. and Thapar, R. and Tovani-Palone, M.R. and Tran, B.X. and Ullah, S. and Tahbaz, S.V. and Violante, F.S. and Vlassov, V. and Vo, B. and Vongpradith, A. and Vu, G.T. and Wei, J. and Yadollahpour, A. and Jabbari, S.H.Y. and Yeshaw, Y. and Yiǧit, V. and Yirdaw, B.W. and Yonemoto, N. and Yu, C. and Yunusa, I. and Zamani, M. and Zastrozhin, M.S. and Zastrozhina, A. and Zhang, Z.-J. and Zhao, J.T. and Murray, C.J.L. and Davis, A.C. and Vos, T. and Chadha, S. and Collaborators, GBD 2019 Hearing Loss (2021) Hearing loss prevalence and years lived with disability, 1990-2019: Findings from the Global Burden of Disease Study 2019. The Lancet, 397 (10278). pp. 996-1009. ISSN 01406736
Hamidi, MOHAMMAD. and Karimipoor, MORTEZA. and Hashemzadeh-Chaleshtori, Morteza. and Akbari, mohammad taghi. (2009) A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients. JOURNAL OF GENETICS, 88 (3). pp. 359-362.
Hashemi, Z and Parvari, R.A and Mirzaeian, Razieh. (2018) Identification of the major sources of noise and noise control techniques in hospitals of Behbahan. Iran Occupational Health, 15 (2).
Hashemzadeh Chaleshtori, M. and Farhud, D.D. and Patton, M.A. (2007) Congratulation to margaret chan familial and sporadic GJB2-Related Deafness in Iran: Review of Gene Mutations. Iranian Journal of Public Health, 36 (1).
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 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.
Hashemzadeh-Chaleshtori, Morteza. and Akbari, mohammad taghi. and Khazraei, Hamid. and Abolhasani, Marzieh. and Reisi, Somayeh and Ataei, Zohreh. and Saedi-Marghmaleki, Mojtaba. and Shirmardi, Seyed Abolfath. and Farrokhi, Effat. and Montazer Zohouri, Mostafa and Azadegan-Dehkordi, Fatemeh. (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).
Hashemzadeh-Chaleshtori, Morteza. and Banitalebi, Golandam. and Reisi, Somayeh and Azadegan-Dehkordi, Fatemeh. and Abolhasani, Marzieh. and Ghasemi, Soraya. and Shirmardi, Seyed Abolfath. and Farrokhi, Effat. and Taherzadeh Ghahfarrokhi, Maryam. (2010) DFNB59 Gene Mutations and its Association with Deafness in Schoolchildren in Kohgilooyeh & Boyerahmad Province. Armaghane danesh, 14 (4).
Hashemzadeh-Chaleshtori, Morteza. and Farhud, D.D. and Taylor, R. and Hadavi, V. and Patton, Michael. and Afzal, A.R. and Gharavi, Mohammad javad. (2002) Deafness–associated connexin 26 gene (GJB2) mutations in Iranian population. Iranian Journal of Public Health, 31 (3-4).
Hashemzadeh-Chaleshtori, Morteza. and Farhud, Daryoush. and Crosby, Andrew.H. and Farrokhi, Effat. and Jafari Pour, H. and Ghatreh Samani, Keihan. and Safa Chaleshtori, K. and Kasiri, Mansureh. and Shahrani, Mehrdad. and Mobini, GholamReza. 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, Morteza. and Farrokhi, Effat. and Shahrani, Mehrdad. and Kheiri, Soleiman. and Dolati, Masoumeh. and Hoghooghi Rad, Laleh. and Pour-Jafari, Hamid. and Ghatreh Samani, Keihan. and Safa Chaleshtori, Katayoon. and Crosby, Andrew 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, Morteza. and Montazer Zohouri, Mostafa. and Hoghooghi Rad, L. and Pour-Jafari, Hamid. and Farhud, Daryoush. and Dolati, M. and Safa Chaleshtori, K. and Sasanfar, Roksana. and Hosseinipour, A. and Andonian, Laris. 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.
Hemati, Zeinab. and Abbasi, Samira. and Paki, Somayeh. and Kiani, Davood. (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, Zeinab. and Derakhshande, Fateme. and Abbasi, Samira. and Kiani, Davood. (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 Hashemzadeh-Chaleshtori, Morteza. and Sasanfar, Roksana. and Farhud, Daryoush. and Tolooi, A. and Doulati, M. and Rad, L.H. and Montazer Zohouri, Mostafa. 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.
Iranmanesh, Sedigheh. and Rafiei, Hossein. and Esmaeili Abdar, Mohammad. (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.
Kamrava, Seyed Kamran and Tavakol, Zeinab and Talebi, Atefeh and Farhadi, Mohammad and Jalessi, Maryam and Hosseini, Seyedeh Fahimeh and Amini, Elahe and Chen, Ben and Hummel, Thomas and Alizadeh, Rafieh (2021) A study of depression, partnership and sexual satisfaction in patients with post-traumatic olfactory disorders. SCIENTIFIC REPORTS, 11 (1).
Karami-Eshkaftaki, Raziyeh. and Ahmadinejad, Fereshteh. and Aghaei, Shahrzad. and Moghim, Hassan. and Hashemzadeh-Chaleshtori, Morteza. and Jami, Mohammad-Saeid. (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 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.
Kargoshaie, Amir. and Akhlaghi, Mahmood. and Najafi, Mostafa. (2009) Oxygen saturation improvement after adenotonsillectomy in children. Pakistan journal of biological sciences : PJBS, 12 (3). pp. 276-80. ISSN 1028-8880
Khatami, Somayeh and Askari, Masomeh and Bahreini, Fatemeh and Hashemzadeh-Chaleshtori, Morteza and Hematian, Saeed and Asgharzade, Samira (2020) Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees. BMC Medical Genetics, 21 (1). ISSN 1471-2350
Khodami, Nasim. and Shahtoosi, Mina. and Amani, Soroush. and khazraei, Hamid reza. and Khodami, Alireza. (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, Abolfazl. and Panahandeh, Gholamreza. and Noorbakhsh, Mohamad Kazem. and Malek Ahmadi, Mohamad Reza. and Lotfizadeh Dehkordi, Masoud. and Parvin, Neda. (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.
Khosrofar, Mahtab. and Pourreza, Mohammad Reza. and Asgharzadeh, Samira. and Tahmasebi, Parisa. and Ali Asgari, Elahe. and Ghasemikhah, Reza. and Saki, Nader. and Mohammadi-Asl, Javad. and Hashemzadeh-Chaleshtori, Morteza. and Tabatabaiefar, Mohammad Amin. (2017) Genetic Linkage Analysis of the DFNB21 Locus in Autosomal Recessive Hearing Loss in Large Families from Khuzestan Province. Arak Medical University Journal, 20 (3).
Koohiyan, M and Ahmadi, A and Koohian, F and Aghaei, S and Amiri, B and Hashemzadeh-Chaleshtori, M (2019) An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review. Int J Pediatr Otorhinolaryngol, 25 (119).
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