Houshmand G - Search Results

1

A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report.

Hesami H, Ghasemi S, Houshmand G, Nilipour Y, Hesami M, Biglari A, Nafissi S, Maleki M, Kalayinia S. Hesami H, et al. Among authors: houshmand g. BMC Musculoskelet Disord. 2024 Mar 27;25(1):241. doi: 10.1186/s12891-024-07354-9. BMC Musculoskelet Disord. 2024. PMID: 38539162 Free PMC article.

2

Endomyocardial Biopsy via the Femoral Vein Using a Long, Curved Sheath.

Naderi N, Taghavi S, Amin A, Houshmand G, Mozaffari K, Maleki M. Naderi N, et al. Among authors: houshmand g. Transplant Proc. 2017 Jul-Aug;49(6):1436-1439. doi: 10.1016/j.transproceed.2017.03.076. Transplant Proc. 2017. PMID: 28736019

3

Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family.

Mahdavi M, Mohsen-Pour N, Maleki M, Hesami M, Naderi N, Houshmand G, Rasouli Jazi HR, Shahzadi H, Kalayinia S. Mahdavi M, et al. Among authors: houshmand g. Cardiol Young. 2021 Nov 16:1-6. doi: 10.1017/S1047951121004455. Online ahead of print. Cardiol Young. 2021. PMID: 34782032

4

Cytokine storm after heart transplantation in COVID-19-related haemophagocytic lymphohistiocytosis (HLH).

Mahdavi M, Hejri GM, Pouraliakbar H, Shahzadi H, Hesami M, Houshmand G. Mahdavi M, et al. Among authors: houshmand g. ESC Heart Fail. 2022 Feb;9(1):219-223. doi: 10.1002/ehf2.13728. Epub 2021 Nov 24. ESC Heart Fail. 2022. PMID: 34821079 Free PMC article.

5

Whole -exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family - CORRIGENDUM.

Mahdavi M, Mohsen-Pour N, Maleki M, Hesami M, Naderi N, Houshmand G, Rasouli Jazi HR, Shahzadi H, Kalayinia S. Mahdavi M, et al. Among authors: houshmand g. Cardiol Young. 2021 Dec 6:1. doi: 10.1017/S1047951121004832. Online ahead of print. Cardiol Young. 2021. PMID: 34865674 No abstract available.

6

Multimodality imaging in the diagnostic approach to a patient with carcinoid heart disease involving four heart valves.

Habibi Khorasani S, Parsaee M, Samiei N, Hesami M, Noohi F, Hosseini S, Houshmand G. Habibi Khorasani S, et al. Among authors: houshmand g. Clin Case Rep. 2022 Jul 25;10(7):e6152. doi: 10.1002/ccr3.6152. eCollection 2022 Jul. Clin Case Rep. 2022. PMID: 35898747 Free PMC article.

7

Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathy.

Kalayinia S, Mahdavi M, Houshmand G, Hesami M, Pourirahim M, Maleki M. Kalayinia S, et al. Among authors: houshmand g. BMC Cardiovasc Disord. 2022 Aug 6;22(1):359. doi: 10.1186/s12872-022-02802-7. BMC Cardiovasc Disord. 2022. PMID: 35933355 Free PMC article.

8

Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy.

Mahdavi M, Mohsen-Pour N, Maleki M, Ghasemi S, Tabib A, Houshmand G, Naderi N, Masoumi T, Pouraliakbar H, Kalayinia S. Mahdavi M, et al. Among authors: houshmand g. Lab Med. 2024 Jan 6;55(1):62-70. doi: 10.1093/labmed/lmad038. Lab Med. 2024. PMID: 37246508

9

Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac death.

Azimi A, Pourirahim M, Houshmand G, Adimi S, Maleki M, Kalayinia S. Azimi A, et al. Among authors: houshmand g. BMC Med Genomics. 2023 Oct 26;16(1):266. doi: 10.1186/s12920-023-01701-w. BMC Med Genomics. 2023. PMID: 37885024 Free PMC article.

10

Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population.

Houshmand G, Alemzadeh-Ansari MJ, Mazloumzadeh S, Naderi N, Pourirahim M, Heshmatzad K, Maleki M, Kalayinia S. Houshmand G, et al. J Cardiovasc Thorac Res. 2023;15(3):168-173. doi: 10.34172/jcvtr.2023.31742. Epub 2023 Sep 23. J Cardiovasc Thorac Res. 2023. PMID: 38028723 Free PMC article.

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