Dastgheib SA - Search Results

1

Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series.

Mahjoub G, Habibzadeh P, Dastsooz H, Mirzaei M, Kavosi A, Jamali L, Javanmardi H, Katibeh P, Faghihi MA, Dastgheib SA. Mahjoub G, et al. Among authors: dastgheib sa. BMC Med Genet. 2019 Oct 29;20(1):167. doi: 10.1186/s12881-019-0893-9. BMC Med Genet. 2019. PMID: 31664948 Free PMC article.

2

Correlation between rs1800871, rs1800872 and rs1800896 Polymorphisms at IL-10 Gene and Lung Cancer Risk.

Vakili M, Shirinzadeh-Dastgiri A, Ershadi R, Dastgheib SA, Shiri A, Aghasipour M, Barahman M, Manzourolhojeh M, Aghili K, Neamatzadeh H, Akbarian E. Vakili M, et al. Among authors: dastgheib sa. Asian Pac J Cancer Prev. 2024 Jan 1;25(1):287-298. doi: 10.31557/APJCP.2024.25.1.287. Asian Pac J Cancer Prev. 2024. PMID: 38285796 Free PMC article.

3

The interaction of breastfeeding and genetic factors on childhood obesity.

Danaie M, Yeganegi M, Dastgheib SA, Bahrami R, Jayervand F, Rahmani A, Aghasipour M, Golshan-Tafti M, Azizi S, Marzbanrad Z, Masoudi A, Shiri A, Lookzadeh MH, Noorishadkam M, Neamatzadeh H. Danaie M, et al. Among authors: dastgheib sa. Eur J Obstet Gynecol Reprod Biol X. 2024 Aug 9;23:100334. doi: 10.1016/j.eurox.2024.100334. eCollection 2024 Sep. Eur J Obstet Gynecol Reprod Biol X. 2024. PMID: 39224127 Free PMC article. Review.

4

A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report.

Ziyaee F, Shorafa E, Dastsooz H, Habibzadeh P, Nemati H, Saeed A, Silawi M, Farazi Fard MA, Faghihi MA, Dastgheib SA. Ziyaee F, et al. Among authors: dastgheib sa. BMC Med Genet. 2019 Jan 14;20(1):13. doi: 10.1186/s12881-018-0743-1. BMC Med Genet. 2019. PMID: 30642275 Free PMC article.

5

Phenotype of ST3GAL3 deficient patients: A case and review of the literature.

Khamirani HJ, Zoghi S, Faghihi F, Dastgheib SA, Hassanipour H, Bagher Tabei SM, Mohammadi S, Masoudi M, Poorang S, Ehsani E, Dianatpour M. Khamirani HJ, et al. Among authors: dastgheib sa. Eur J Med Genet. 2021 Aug;64(8):104250. doi: 10.1016/j.ejmg.2021.104250. Epub 2021 May 20. Eur J Med Genet. 2021. PMID: 34022416 Review.

6

A novel non-sense mutation in TDP2 causes spinocerebellar ataxia autosomal recessive 23 accompanied by bilateral upward gaze; report of a case and review of the literature.

Zoghi S, Khamirani HJ, Hassanipour H, Bostanian P, Masoudian R, Dastgheib SA. Zoghi S, et al. Among authors: dastgheib sa. Eur J Med Genet. 2021 Dec;64(12):104348. doi: 10.1016/j.ejmg.2021.104348. Epub 2021 Oct 1. Eur J Med Genet. 2021. PMID: 34606976 Review.

7

Clinical features of patients with Yin Yang 1 deficiency causing Gabriele-de Vries syndrome: A new case and review of the literature.

Khamirani HJ, Zoghi S, Namdar ZM, Kamal N, Dianatpour M, Tabei SMB, Mohammadi S, Dehghanian F, Farbod Z, Dastgheib SA. Khamirani HJ, et al. Among authors: dastgheib sa. Ann Hum Genet. 2022 Jan;86(1):52-62. doi: 10.1111/ahg.12448. Epub 2021 Nov 3. Ann Hum Genet. 2022. PMID: 34729769 Review.

8

ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review.

Kamal N, Khamirani HJ, Mohammadi S, Dastgheib SA, Dianatpour M, Tabei SMB. Kamal N, et al. Among authors: dastgheib sa. Eur J Med Genet. 2022 Jul;65(7):104522. doi: 10.1016/j.ejmg.2022.104522. Epub 2022 May 23. Eur J Med Genet. 2022. PMID: 35618198 Review.

9

Genotypic and phenotypic spectrum of Myofibrillar Myopathy 7 as a result of Kyphoscoliosis Peptidase deficiency: The first description of a missense mutation in KY and literature review.

Ehsani E, Khamirani HJ, Abbasi Z, Gohari M, Zoghi S, Mohammadi S, Dianatpour M, Tabei SMB, Mohamadjani O, Dastgheib SA. Ehsani E, et al. Among authors: dastgheib sa. Eur J Med Genet. 2022 Aug;65(8):104552. doi: 10.1016/j.ejmg.2022.104552. Epub 2022 Jun 22. Eur J Med Genet. 2022. PMID: 35752288 Review.

10

The third patient of ACACA-related acetyl-CoA carboxylase deficiency with seizure and literature review.

Shafieipour N, Jafari Khamirani H, Kamal N, Tabei SMB, Dianatpour M, Dastgheib SA. Shafieipour N, et al. Among authors: dastgheib sa. Eur J Med Genet. 2023 Apr;66(4):104707. doi: 10.1016/j.ejmg.2023.104707. Epub 2023 Jan 26. Eur J Med Genet. 2023. PMID: 36709796 Review.

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