Zare-Abdollahi D - Search Results

1

A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.

Darbari E, Zare-Abdollahi D, Alavi A, Rezaei Kanavi M, Feizi S, Hosseini SB, Baradaran-Rafii A, Ahmadieh H, Issazadeh-Navikas S, Elahi E. Darbari E, et al. Among authors: zare abdollahi d. Mol Vis. 2020 Nov 25;26:757-765. eCollection 2020. Mol Vis. 2020. PMID: 33273802 Free PMC article.

2

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. Ophthalmic Genet. 2019 Apr;40(2):141-145. doi: 10.1080/13816810.2019.1592200. Epub 2019 Apr 22. Ophthalmic Genet. 2019. PMID: 31006324

3

The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.

Pashaei M, Rahimi Bidgoli MM, Zare-Abdollahi D, Najmabadi H, Haji-Seyed-Javadi R, Fatehi F, Alavi A. Pashaei M, et al. J Assist Reprod Genet. 2020 Feb;37(2):451-458. doi: 10.1007/s10815-019-01660-1. Epub 2020 Jan 8. J Assist Reprod Genet. 2020. PMID: 31916078 Free PMC article.

4

Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigree.

Alavi A, Darki F, Bidgoli MMR, Zare-Abdollahi D, Moini A, Shahshahani MM, Fischer J, Elahi E. Alavi A, et al. Among authors: zare abdollahi d. Mol Genet Genomics. 2020 Jul;295(4):1039-1053. doi: 10.1007/s00438-020-01663-z. Epub 2020 Apr 6. Mol Genet Genomics. 2020. PMID: 32253496

5

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. Among authors: zare abdollahi d. 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.

6

Clinical spectrum in multiple families with primary COQ₁₀ deficiency.

Hashemi SS, Zare-Abdollahi D, Bakhshandeh MK, Vafaee A, Abolhasani S, Inanloo Rahatloo K, DanaeeFard F, Farboodi N, Rohani M, Alavi A. Hashemi SS, et al. Among authors: zare abdollahi d. Am J Med Genet A. 2021 Feb;185(2):440-452. doi: 10.1002/ajmg.a.61983. Epub 2020 Nov 20. Am J Med Genet A. 2021. PMID: 33215859

7

A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population.

Sadr Z, Zare-Abdollahi D, Rohani M, Alavi A. Sadr Z, et al. Among authors: zare abdollahi d. Neurol Sci. 2023 Jul;44(7):2599-2602. doi: 10.1007/s10072-023-06707-x. Epub 2023 Mar 1. Neurol Sci. 2023. PMID: 36854932 No abstract available.

8

Giant axonal neuropathy: The first Iranian case with a variation in the gigaxonin gene and a glance to the other cases.

Vafaee-Shahi M, Ghasemi S, Ghahvechi-Akbar M, Tahernia L, Davarzani A, Hajati R, Zare-Abdollahi D, Alavi A. Vafaee-Shahi M, et al. Among authors: zare abdollahi d. Curr J Neurol. 2020 Oct 6;19(4):200-210. doi: 10.18502/cjn.v19i4.5548. Curr J Neurol. 2020. PMID: 38011432 Free PMC article.

9

An Iranian family with azoospermia and premature ovarian insufficiency segregating NR5A1 mutation.

Safari S, Zare-Abdollahi D, Mirfakhraie R, Ghafouri-Fard S, Pouresmaeili F, Movafagh A, Omrani MD. Safari S, et al. Climacteric. 2014 Jun;17(3):301-3. doi: 10.3109/13697137.2013.847079. Epub 2013 Oct 28. Climacteric. 2014. PMID: 24067197

10

Intact expression status of RASSF1A in acute myeloid leukemia.

Zare-Abdollahi D, Safari S, Movafagh A, Ghadiani M, Riazi-Isfahani S, Omrani MD. Zare-Abdollahi D, et al. Med Oncol. 2014 Jan;31(1):770. doi: 10.1007/s12032-013-0770-x. Epub 2013 Nov 19. Med Oncol. 2014. PMID: 24248815

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