Nilforoush MH - Search Results

1

A Prevalence Study of Hearing Loss among Primary School Children in the South East of Iran.

Absalan A, Pirasteh I, Dashti Khavidaki GA, Asemi Rad A, Nasr Esfahani AA, Nilforoush MH. Absalan A, et al. Among authors: nilforoush mh. Int J Otolaryngol. 2013;2013:138935. doi: 10.1155/2013/138935. Epub 2013 Jul 1. Int J Otolaryngol. 2013. PMID: 23935628 Free PMC article.

2

The occurrence of laryngeal penetration and aspiration in patients with glottal closure insufficiency.

Rajaei A, Barzegar Bafrooei E, Mojiri F, Nilforoush MH. Rajaei A, et al. Among authors: nilforoush mh. ISRN Otolaryngol. 2014 Mar 11;2014:587945. doi: 10.1155/2014/587945. eCollection 2014. ISRN Otolaryngol. 2014. PMID: 24891957 Free PMC article.

3

Ear surgery techniques results on hearing threshold improvement.

Mokhtarinejad F, Pour SS, Nilforoush MH, Sepehrnejad M, Mirelahi S. Mokhtarinejad F, et al. Among authors: nilforoush mh. J Res Med Sci. 2013 Sep;18(9):746-9. J Res Med Sci. 2013. PMID: 24381615 Free PMC article.

4

Validation of the persian translation of the swallowing disturbance questionnaire in Parkinson's disease patients.

Rajaei A, Azargoon SA, Nilforoush MH, Barzegar Bafrooei E, Ashtari F, Chitsaz A. Rajaei A, et al. Among authors: nilforoush mh. Parkinsons Dis. 2014;2014:159476. doi: 10.1155/2014/159476. Epub 2014 Oct 27. Parkinsons Dis. 2014. PMID: 25405058 Free PMC article.

5

The association between saliva control, silent saliva penetration, aspiration, and videofluoroscopic findings in Parkinson's disease patients.

Rajaei A, Ashtari F, Azargoon SA, Chitsaz A, Nilforoush MH, Taheri M, Sadeghi S. Rajaei A, et al. Among authors: nilforoush mh. Adv Biomed Res. 2015 May 29;4:108. doi: 10.4103/2277-9175.157815. eCollection 2015. Adv Biomed Res. 2015. PMID: 26261810 Free PMC article.

6

A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.

Sarmadi A, Nasrniya S, Soleimani Farsani M, Narrei S, Nouri Z, Sepehrnejad M, Nilforoush MH, Abtahi H, Tabatabaiefar MA. Sarmadi A, et al. Among authors: nilforoush mh. BMC Med Genet. 2020 Jun 9;21(1):127. doi: 10.1186/s12881-020-01061-7. BMC Med Genet. 2020. PMID: 32517708 Free PMC article.

7

Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.

Nasrniya S, Miar P, Narrei S, Sepehrnejad M, Nilforoush MH, Abtahi H, Tabatabaiefar MA. Nasrniya S, et al. Among authors: nilforoush mh. Lab Med. 2022 Mar 7;53(2):111-122. doi: 10.1093/labmed/lmab047. Lab Med. 2022. PMID: 34388253

8

A Novel Biallelic Variant in CDH23 Gene in a Family with Atypical USH1D Manifestation: A Literature Review and Investigation of Genotype-Phenotype Correlation.

Khorram E, Iravani O, Khorrami M, Amini M, Jahanian S, Nilforoush MH, Mousavi SR, Ehsanifard M, Kheirollahi M. Khorram E, et al. Among authors: nilforoush mh. Audiol Neurootol. 2023;28(4):317-326. doi: 10.1159/000529420. Epub 2023 Apr 21. Audiol Neurootol. 2023. PMID: 37088079 Review.

9

Wideband Tympanometry: Normative Data for Young Iranian Adults.

Habibi Z, Sepehrnejad M, Rahimi Ghooradel F, Nilforoush MH. Habibi Z, et al. Among authors: nilforoush mh. Audiol Neurootol. 2023;28(1):22-31. doi: 10.1159/000526380. Epub 2022 Sep 22. Audiol Neurootol. 2023. PMID: 36137525

10

Effect of transcranial direct current stimulation on short-term and long-term treatment of chronic tinnitus.

Abtahi H, Okhovvat A, Heidari S, Gharagazarloo A, Mirdamadi M, Nilforoush MH, Ghazavi H. Abtahi H, et al. Among authors: nilforoush mh. Am J Otolaryngol. 2018 Mar-Apr;39(2):94-96. doi: 10.1016/j.amjoto.2018.01.001. Epub 2018 Jan 6. Am J Otolaryngol. 2018. PMID: 29336898 Clinical Trial.

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