Nafissi S - Search Results

1

Correlation between distribution of muscle weakness, electrophysiological findings and CTG expansion in myotonic dystrophy.

Khoshbakht R, Soltanzadeh A, Zamani B, Abdi S, Gharagozli K, Kahrizi K, Khoshbakht R, Nafissi S. Khoshbakht R, et al. Among authors: nafissi s. J Clin Neurosci. 2014 Jul;21(7):1123-6. doi: 10.1016/j.jocn.2013.09.016. Epub 2013 Nov 18. J Clin Neurosci. 2014. PMID: 24417793

2

Wilson's disease: a great masquerader.

Soltanzadeh A, Soltanzadeh P, Nafissi S, Ghorbani A, Sikaroodi H, Lotfi J. Soltanzadeh A, et al. Among authors: nafissi s. Eur Neurol. 2007;57(2):80-5. doi: 10.1159/000098056. Epub 2006 Dec 15. Eur Neurol. 2007. PMID: 17179709

3

Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients.

Alavi A, Nafissi S, Rohani M, Zamani B, Sedighi B, Shamshiri H, Fan JB, Ronaghi M, Elahi E. Alavi A, et al. Among authors: nafissi s. Neurobiol Aging. 2013 May;34(5):1516.e1-8. doi: 10.1016/j.neurobiolaging.2012.09.006. Epub 2012 Oct 9. Neurobiol Aging. 2013. PMID: 23062701

4

Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients.

Alavi A, Nafissi S, Rohani M, Shahidi G, Zamani B, Shamshiri H, Safari I, Elahi E. Alavi A, et al. Among authors: nafissi s. Neurobiol Aging. 2014 Jan;35(1):267.e1-7. doi: 10.1016/j.neurobiolaging.2013.07.016. Epub 2013 Aug 17. Neurobiol Aging. 2014. PMID: 23962495

5

Chronic inflammatory demyelinating polyneuropathy associated with diabetes mellitus.

Fatehi F, Nafissi S, Basiri K, Amiri M, Soltanzadeh A. Fatehi F, et al. Among authors: nafissi s. J Res Med Sci. 2013 May;18(5):438-41. J Res Med Sci. 2013. PMID: 24174953 Free PMC article. Review.

6

Clinical and electrophysiological features of Guillain-Barré syndrome in Iran.

Yadegari S, Kazemi N, Nafissi S. Yadegari S, et al. Among authors: nafissi s. J Clin Neurosci. 2014 Sep;21(9):1554-7. doi: 10.1016/j.jocn.2013.11.041. Epub 2014 Apr 29. J Clin Neurosci. 2014. PMID: 24786718

7

Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathy.

Fattahi Z, Kahrizi K, Nafissi S, Fadaee M, Abedini SS, Kariminejad A, Akbari MR, Najmabadi H. Fattahi Z, et al. Among authors: nafissi s. Arch Iran Med. 2015 Jan;18(1):60-4. Arch Iran Med. 2015. PMID: 25556389

8

Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study.

Shamshiri H, Fatehi F, Davoudi F, Mir E, Pourmirza B, Abolfazli R, Etemadifar M, Harirchian MH, Gharagozli K, Ayromlou H, Basiri K, Zamani B, Rohani M, Sedighi B, Roudbari A, Delavar Kasmaei H, Nikkhah K, Ranjbar Naeini A, Nafissi S. Shamshiri H, et al. Among authors: nafissi s. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(7-8):506-11. doi: 10.3109/21678421.2015.1074698. Epub 2015 Oct 5. Amyotroph Lateral Scler Frontotemporal Degener. 2015. PMID: 26437387

9

Report of limb girdle muscular dystrophy type 2a in 6 Iranian patients, one with a novel deletion in CAPN3 gene.

Fadaee M, Kariminejad A, Fattahi Z, Nafissi S, Godarzi HR, Beheshtian M, Vazehan R, Akbari MR, Kahrizi K, Najmabadi H. Fadaee M, et al. Among authors: nafissi s. Neuromuscul Disord. 2016 Apr-May;26(4-5):277-82. doi: 10.1016/j.nmd.2016.02.003. Epub 2016 Feb 15. Neuromuscul Disord. 2016. PMID: 27020652

10

Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population.

Fattahi Z, Kalhor Z, Fadaee M, Vazehan R, Parsimehr E, Abolhassani A, Beheshtian M, Zamani G, Nafissi S, Nilipour Y, Akbari MR, Kahrizi K, Kariminejad A, Najmabadi H. Fattahi Z, et al. Among authors: nafissi s. Clin Genet. 2017 Mar;91(3):386-402. doi: 10.1111/cge.12810. Epub 2016 Jul 21. Clin Genet. 2017. PMID: 27234031

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