Bushehri A - Search Results

1

Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability.

Fattahi M, Bushehri A, Alavi A, Asghariazar V, Nozari A, Ghasemi Firouzabadi S, Motamedian Dehkordi P, Javid M, Farajzadeh Valiliou S, Karimian J, Behjati F. Fattahi M, et al. Among authors: bushehri a. Gene. 2020 Jul 1:144918. doi: 10.1016/j.gene.2020.144918. Online ahead of print. Gene. 2020. PMID: 32621952

2

Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa.

Bushehri A, Zare-Abdollahi D, Alavi A, Dehghani A, Mousavimikala M, Khorram Khorshid HR. Bushehri A, et al. Int J Mol Cell Med. 2019 Summer;8(3):179-190. doi: 10.22088/IJMCM.BUMS.8.3.179. Int J Mol Cell Med. 2019. PMID: 32489947 Free PMC article.

3

MFSD8 gene mutations; evidence for phenotypic heterogeneity.

Zare-Abdollahi D, Bushehri A, Alavi A, Dehghani A, Mousavi-Mirkala M, Effati J, Miratashi SAM, Dehani M, Jamali P, Khorram Khorshid HR. Zare-Abdollahi D, et al. Among authors: bushehri a. Ophthalmic Genet. 2019 Apr;40(2):141-145. doi: 10.1080/13816810.2019.1592200. Epub 2019 Apr 22. Ophthalmic Genet. 2019. PMID: 31006324

4

RPE65 and retinal dystrophy: Report of new and recurrent mutations.

Safari S, Zare-Abdollahi D, Bushehri A, Safari MR, Dehghani A, Tahmasebi Z, Khorram Khorshid HR, Ghadami M. Safari S, et al. Among authors: bushehri a. J Gene Med. 2020 Mar;22(3):e3154. doi: 10.1002/jgm.3154. Epub 2020 Jan 19. J Gene Med. 2020. PMID: 31957135

5

Genome-wide identification of human- and primate-specific core promoter short tandem repeats.

Bushehri A, Barez MR, Mansouri SK, Biglarian A, Ohadi M. Bushehri A, et al. Gene. 2016 Aug 1;587(1):83-90. doi: 10.1016/j.gene.2016.04.041. Epub 2016 Apr 22. Gene. 2016. PMID: 27108803

6

Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia.

Bushehri A, Zare-Abdollahi D, Hashemian H, Safavizadeh L, Effati J, Khorram Khorshid HR. Bushehri A, et al. Iran Biomed J. 2020 Jul;24(4):257-63. doi: 10.29252/ibj.24.4.257. Epub 2020 Dec 28. Iran Biomed J. 2020. PMID: 32306724 Free PMC article.

7

Identification of a Novel Homozygous Mutation in BBS10 Gene in an Iranian Family with Bardet-Biedl Syndrome.

Dehani M, Zare-Abdollahi D, Bushehri A, Dehghani A, Effati J, Miratashi SAM, Khorram Khorshid HR. Dehani M, et al. Among authors: bushehri a. Avicenna J Med Biotechnol. 2021 Oct-Dec;13(4):230-233. Avicenna J Med Biotechnol. 2021. PMID: 34900151 Free PMC article.

8

Peer Review in Radiation Oncology: Where Does the Middle East, North Africa, and Türkiye Region Stand?

Abutaha S, Mula-Hussain L, ElHaddad M, Sami S, Ammar K, Dahbi Z, Jabbour C, Selek U, Abu-Hijlih R, Al-Ibraheem A, Abuhijla F, Abbasi A, Bushehri A, Alotain I, Aldehaim M, Alghamdi M, Abu-Gheida I, Pervez N, Youssef B, Alrashidi S, El-Sheshtawy W, Hosni A, Mohamad I. Abutaha S, et al. Among authors: bushehri a. JCO Glob Oncol. 2024 Aug;10:e2400229. doi: 10.1200/GO.24.00229. JCO Glob Oncol. 2024. PMID: 39208368

9

The Evolving Role of Stereotactic Body Radiation Therapy for Head and Neck Cancer: Where Do We Stand?

Mohamad I, Karam I, El-Sehemy A, Abu-Gheida I, Al-Ibraheem A, Al-Assaf H, Aldehaim M, Alghamdi M, Alotain I, Ashour M, Bushehri A, ElHaddad M, Hosni A. Mohamad I, et al. Among authors: bushehri a. Cancers (Basel). 2023 Oct 16;15(20):5010. doi: 10.3390/cancers15205010. Cancers (Basel). 2023. PMID: 37894377 Free PMC article. Review.

10

Radiation-induced nausea and vomiting: a comparison between MASCC/ESMO, ASCO, and NCCN antiemetic guidelines.

McKenzie E, Zaki P, Raman S, Olson R, McFarlane T, DeAngelis C, Chan S, Pidduck W, Razvi Y, Bushehri A, Chow E. McKenzie E, et al. Among authors: bushehri a. Support Care Cancer. 2019 Mar;27(3):783-791. doi: 10.1007/s00520-018-4586-2. Epub 2019 Jan 3. Support Care Cancer. 2019. PMID: 30607675 Review.

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