Kahrizi K - 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: kahrizi k. 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

CTG expansion & haplotype analysis in DM1 gene in healthy Iranian population.

Shojasaffar B, Moradin N, Kahrizi K, Cobo AM, Najmabadi H. Shojasaffar B, et al. Among authors: kahrizi k. Can J Neurol Sci. 2008 May;35(2):216-9. doi: 10.1017/s0317167100008660. Can J Neurol Sci. 2008. PMID: 18574937

3

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: kahrizi k. Arch Iran Med. 2015 Jan;18(1):60-4. Arch Iran Med. 2015. PMID: 25556389

4

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: kahrizi k. 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

5

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: kahrizi k. Clin Genet. 2017 Mar;91(3):386-402. doi: 10.1111/cge.12810. Epub 2016 Jul 21. Clin Genet. 2017. PMID: 27234031

6

LGMD2E is the most common type of sarcoglycanopathies in the Iranian population.

Alavi A, Esmaeili S, Nilipour Y, Nafissi S, Tonekaboni SH, Zamani G, Ashrafi MR, Kahrizi K, Najmabadi H, Jazayeri F. Alavi A, et al. Among authors: kahrizi k. J Neurogenet. 2017 Sep;31(3):161-169. doi: 10.1080/01677063.2017.1346093. Epub 2017 Jul 7. J Neurogenet. 2017. PMID: 28687063

7

Genotype and phenotype analysis of 43 Iranian facioscapulohumeral muscular dystrophy patients; Evidence for anticipation.

Alavi A, Esmaeili S, Nafissi S, Kahrizi K, Najmabadi H. Alavi A, et al. Among authors: kahrizi k. Neuromuscul Disord. 2018 Apr;28(4):303-314. doi: 10.1016/j.nmd.2018.01.001. Epub 2018 Jan 12. Neuromuscul Disord. 2018. PMID: 29402602

8

Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum.

Taghizadeh S, Vazehan R, Beheshtian M, Sadeghinia F, Fattahi Z, Mohseni M, Arzhangi S, Nafissi S, Kariminejad A, Najmabadi H, Kahrizi K. Taghizadeh S, et al. Among authors: kahrizi k. Arch Iran Med. 2020 Jul 1;23(7):426-433. doi: 10.34172/aim.2020.39. Arch Iran Med. 2020. PMID: 32657593 Free article.

9

Expanding the Molecular Spectrum of HK1-Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in Iran.

Goleyjani Moghadam M, Elahi Z, Soveyzi M, Arzhangi S, Nafissi S, Najmabadi H, Kahrizi K, Fattahi Z. Goleyjani Moghadam M, et al. Among authors: kahrizi k. Arch Iran Med. 2023 May 1;26(5):279-284. doi: 10.34172/aim.2023.43. Arch Iran Med. 2023. PMID: 38301092 Free PMC article.

10

Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.

Abolhassani A, Fattahi Z, Beheshtian M, Fadaee M, Vazehan R, Ahangari F, Dehdahsi S, Faraji Zonooz M, Parsimehr E, Kalhor Z, Peymani F, Mozaffarpour Nouri M, Babanejad M, Noudehi K, Fatehi F, Zamanian Najafabadi S, Afroozan F, Yazdan H, Bozorgmehr B, Azarkeivan A, Sadat Mahdavi S, Nikuei P, Fatehi F, Jamali P, Ashrafi MR, Karimzadeh P, Habibi H, Kahrizi K, Nafissi S, Kariminejad A, Najmabadi H. Abolhassani A, et al. Among authors: kahrizi k. NPJ Genom Med. 2024 Feb 19;9(1):12. doi: 10.1038/s41525-024-00393-0. NPJ Genom Med. 2024. PMID: 38374194 Free PMC article.

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