Nouri N - 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: nouri n. J Child Neurol. 2015 Apr;30(5):558-62. doi: 10.1177/0883073814521297. Epub 2014 Feb 20. J Child Neurol. 2015. PMID: 24563475

2

A novel mutation in the aprataxin (APTX) gene in an Iranian individual suffering early-onset ataxia with oculomotor apraxia type 1(AOA1) disease.

Nouri N, Nouri N, Aryani O, Kamalidehghan B, Sedghi M, Houshmand M. Nouri N, et al. Iran Biomed J. 2012;16(4):223-5. doi: 10.6091/ibj.1077.2012. Iran Biomed J. 2012. PMID: 23183622 Free PMC article.

3

Cutis laxa type II with mutation in the pyrroline-5-carboxylate reductase 1 gene.

Nouri N, Aryani O, Nouri N, Kamalidehghan B, Houshmand M. Nouri N, et al. Pediatr Dermatol. 2013 Nov-Dec;30(6):e265-7. doi: 10.1111/pde.12065. Epub 2013 Feb 14. Pediatr Dermatol. 2013. PMID: 23406396

4

Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries.

Nouri N, Fazel-Najafabadi E, Behnam M, Nouri N, Aryani O, Ghasemi M, Nasiri J, Sedghi M. Nouri N, et al. Gene. 2014 Feb 10;535(2):250-4. doi: 10.1016/j.gene.2013.11.022. Epub 2013 Nov 22. Gene. 2014. PMID: 24274981

5

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. 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.

6

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: nouri n. 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.

7

Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects.

Ganji H, Salehi M, Sedghi M, Abdali H, Nouri N, Sadri L, Hosseinzadeh M, Vakili B, Lotfi M. Ganji H, et al. Among authors: nouri n. Heart Asia. 2013 Sep 12;5(1):200-2. doi: 10.1136/heartasia-2013-010327. eCollection 2013. Heart Asia. 2013. PMID: 27326128 Free PMC article.

8

An insight into genetics of non-syndromic cleft palate.

Nouri N, Karimi P, Mansoor S, Memarzadeh M, Ganji H, Sedghi M. Nouri N, et al. Adv Biomed Res. 2013 Mar 6;2:6. doi: 10.4103/2277-9175.107969. Print 2013. Adv Biomed Res. 2013. PMID: 23930251 Free PMC article.

9

Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsy.

Nouri N, Bahreini A, Nasiri J, Salehi M. Nouri N, et al. Epilepsy Res. 2021 Nov;177:106782. doi: 10.1016/j.eplepsyres.2021.106782. Epub 2021 Oct 5. Epilepsy Res. 2021. PMID: 34695666

10

A case report of 22q11 deletion syndrome confirmed by array-CGH method.

Sedghi M, Nouri N, Abdali H, Memarzadeh M, Nouri N. Sedghi M, et al. Among authors: nouri n. J Res Med Sci. 2012 Mar;17(3):310-2. J Res Med Sci. 2012. PMID: 23267387 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

162 results

Search Page

Filters