Dehghan Tezerjani M - Search Results

1

A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II).

Dehghan Tezerjani M, Vahidi Mehrjardi MY, Hozhabri H, Rahmanian M. Dehghan Tezerjani M, et al. Front Pediatr. 2020 Jun 25;8:340. doi: 10.3389/fped.2020.00340. eCollection 2020. Front Pediatr. 2020. PMID: 32671003 Free PMC article.

2

Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report.

Vahidi Mehrjardi MY, Dehghan Tezerjani M, Nori-Shadkam M, Kalantar SM, Dehghani M. Vahidi Mehrjardi MY, et al. Among authors: dehghan tezerjani m. Iran J Public Health. 2016 Mar;45(3):376-80. Iran J Public Health. 2016. PMID: 27141501 Free PMC article.

3

A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report.

Dehghan Tezerjani M, Maroofian R, Vahidi Mehrjardi MY, Chioza BA, Zamaninejad S, Kalantar SM, Nori-Shadkam M, Ghadimi H, Baple EL, Crosby AH, Dehghani M. Dehghan Tezerjani M, et al. Iran J Public Health. 2016 Oct;45(10):1359-1366. Iran J Public Health. 2016. PMID: 27957444 Free PMC article.

4

A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous Families.

Dehghani M, Dehghan Tezerjani M, Metanat Z, Vahidi Mehrjardi MY. Dehghani M, et al. Among authors: dehghan tezerjani m. Int J Mol Cell Med. 2017 Spring;6(2):131-134. doi: 10.22088/acadpub.BUMS.6.2.7. Epub 2017 Jun 6. Int J Mol Cell Med. 2017. PMID: 28890889 Free PMC article.

5

Molecular biomarkers in diabetes mellitus (DM).

Aghaei Zarch SM, Dehghan Tezerjani M, Talebi M, Vahidi Mehrjardi MY. Aghaei Zarch SM, et al. Among authors: dehghan tezerjani m. Med J Islam Repub Iran. 2020 Apr 1;34:28. doi: 10.34171/mjiri.34.28. eCollection 2020. Med J Islam Repub Iran. 2020. PMID: 32617267 Free PMC article. Review.

6

Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes.

Sadeghzadeh S, Dehghani Ashkezari M, Seifati SM, Vahidi Mehrjardi MY, Dehghan Tezerjani M, Sadeghzadeh S, Ladan SAB. Sadeghzadeh S, et al. Among authors: dehghan tezerjani m. Diabetes Metab Syndr Obes. 2020 Oct 2;13:3461-3469. doi: 10.2147/DMSO.S263883. eCollection 2020. Diabetes Metab Syndr Obes. 2020. PMID: 33061506 Free PMC article.

7

Incomplete penetrance of autosomal recessive anophthalmia in a large consanguineous family.

Dehghan Tezerjani M, Fathi Dizaji B, Metanat Z, Vahidi Mehrjardi MY. Dehghan Tezerjani M, et al. Ophthalmic Genet. 2021 Dec;42(6):787-789. doi: 10.1080/13816810.2021.1955276. Epub 2021 Jul 21. Ophthalmic Genet. 2021. PMID: 34287093 No abstract available.

8

Association study of ESR1 rs9340799, rs2234693, and MMP2 rs243865 variants in Iranian women with premature ovarian insufficiency: A case-control study.

Sadat Eshaghi F, Dehghan Tezerjani M, Ghasemi N, Dehghani M. Sadat Eshaghi F, et al. Among authors: dehghan tezerjani m. Int J Reprod Biomed. 2022 Nov 2;20(10):841-850. doi: 10.18502/ijrm.v20i10.12268. eCollection 2022 Oct. Int J Reprod Biomed. 2022. PMID: 36381354 Free PMC article.

9

Association of GSTP1, GSTT1 and GSTM1 Gene Variants with Coronary Artery Disease in Iranian Population: A Case-Control Study.

Pourkeramati A, Zare Mehrjardi E, Dehghan Tezerjani M, Seifati SM. Pourkeramati A, et al. Among authors: dehghan tezerjani m. Int J Gen Med. 2020 May 28;13:249-259. doi: 10.2147/IJGM.S252552. eCollection 2020. Int J Gen Med. 2020. PMID: 32547167 Free PMC article.

10

Frequency of TNFR1 36 A/G gene polymorphism in azoospermic infertile men: A case-control study.

Ashrafzadeh HR, Nazari T, Dehghan Tezerjani M, Khademi Bami M, Ghasemi-Esmailabad S, Ghasemi N. Ashrafzadeh HR, et al. Among authors: dehghan tezerjani m. Int J Reprod Biomed. 2017 Aug;15(8):521-526. Int J Reprod Biomed. 2017. PMID: 29082371 Free PMC article.

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