Salehi M - Search Results

1

Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1.

Ganji H, Nouri N, Salehi M, Aryani O, Houshmand M, Basiri K, Fazel-Najafabadi E, Sedghi M. Ganji H, et al. Among authors: salehi m. J Child Neurol. 2015 Apr;30(5):558-62. doi: 10.1177/0883073814521297. Epub 2014 Feb 20. J Child Neurol. 2015. PMID: 24563475

2

Association between mismatch repair gene MSH3 codons 1036 and 222 polymorphisms and sporadic prostate cancer in the Iranian population.

Jafary F, Salehi M, Sedghi M, Nouri N, Jafary F, Sadeghi F, Motamedi S, Talebi M. Jafary F, et al. Among authors: salehi m. Asian Pac J Cancer Prev. 2012;13(12):6055-7. doi: 10.7314/apjcp.2012.13.12.6055. Asian Pac J Cancer Prev. 2012. PMID: 23464402 Free article.

3

Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures.

Meamar R, Ostadsharif M, Saadatnia M, Ghorbani A, Nouri N, Dehghani L, Salehi M. Meamar R, et al. Among authors: salehi m. J Res Med Sci. 2013 Mar;18(Suppl 1):S6-S10. J Res Med Sci. 2013. PMID: 23961289 Free PMC article.

4

Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset.

Nouri N, Fazel-Najafabadi E, Salehi M, Hosseinzadeh M, Behnam M, Ghazavi MR, Sedghi M. Nouri N, et al. Among authors: salehi m. Adv Biomed Res. 2014 Jan 27;3:72. doi: 10.4103/2277-9175.125862. eCollection 2014. Adv Biomed Res. 2014. PMID: 24627880 Free PMC article.

5

Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran.

Sedghi M, Behnam M, Fazel E, Salehi M, Ganji H, Meamar R, Hosseinzadeh M, Nouri N. Sedghi M, et al. Among authors: salehi m. Adv Biomed Res. 2014 Jan 27;3:74. doi: 10.4103/2277-9175.125872. eCollection 2014. Adv Biomed Res. 2014. PMID: 24627882 Free PMC article.

6

Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population.

Nouri N, Memarzadeh M, Carinci F, Cura F, Scapoli L, Nouri N, Jafary F, Sedghi M, Sadri L, Salehi M. Nouri N, et al. Among authors: salehi m. Clin Oral Investig. 2015 May;19(4):891-4. doi: 10.1007/s00784-014-1305-3. Epub 2014 Sep 16. Clin Oral Investig. 2015. PMID: 25220223

7

A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family.

Keivani A, Haghighat-Nia A, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M. Keivani A, et al. Among authors: salehi m. Int J Pediatr Otorhinolaryngol. 2015 Apr;79(4):553-6. doi: 10.1016/j.ijporl.2015.01.027. Epub 2015 Jan 30. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25708704

8

Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation.

Behnam M, Ghorbani F, Shin JH, Kim DS, Jang H, Nouri N, Sedghi M, Salehi M, Ansari B, Basiri K. Behnam M, et al. Among authors: salehi m. Gene. 2015 Oct 1;570(1):150-2. doi: 10.1016/j.gene.2015.06.033. Epub 2015 Jun 15. Gene. 2015. PMID: 26086902

9

Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran.

Haghighat-Nia A, Keivani A, Nadeali Z, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M. Haghighat-Nia A, et al. Among authors: salehi m. Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1892-5. doi: 10.1016/j.ijporl.2015.08.039. Epub 2015 Sep 2. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26409293

10

Non-syndromic cleft lip with or without cleft palate in Asian populations: Association analysis on three gene polymorphisms of the folate pathway.

Martinelli M, Girardi A, Cura F, Nouri N, Pinto V, Carinci F, Morselli PG, Salehi M, Scapoli L. Martinelli M, et al. Among authors: salehi m. Arch Oral Biol. 2016 Jan;61:79-82. doi: 10.1016/j.archoralbio.2015.10.019. Epub 2015 Oct 27. Arch Oral Biol. 2016. PMID: 26540672

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