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Page 1
Infected Ruptured Pseudo-aneurysm in Descending Aorta; a Case Report.
Sanei Taheri M, Nekooghadam SM, Tabatabaei ZS, Rezaei S. Sanei Taheri M, et al. Among authors: tabatabaei zs. Arch Acad Emerg Med. 2024 Jan 7;12(1):e23. doi: 10.22037/aaem.v12i1.2203. eCollection 2024. Arch Acad Emerg Med. 2024. PMID: 38572220 Free PMC article.
Prenatal diagnosis of Sex determining region Y -box transcription factor 2 anophthalmia syndrome caused by germline mosaicism using next-generation sequencing: A case report.
Nikuei P, Ph D, Khashavy Z, Ali Farazi Fard M, Tabasi S, Zeidi B Sc Student A, Pourkashani P, Tabatabaei Z, Eftekhar E, Saberi M, Mahjoubi F. Nikuei P, et al. Among authors: tabatabaei z. Int J Reprod Biomed. 2023 Sep 20;21(8):667-672. doi: 10.18502/ijrm.v21i8.14022. eCollection 2023 Aug. Int J Reprod Biomed. 2023. PMID: 37885978 Free PMC article.
Deep Learning for Skin Melanocytic Tumors in Whole-Slide Images: A Systematic Review.
Mosquera-Zamudio A, Launet L, Tabatabaei Z, Parra-Medina R, Colomer A, Oliver Moll J, Monteagudo C, Janssen E, Naranjo V. Mosquera-Zamudio A, et al. Among authors: tabatabaei z. Cancers (Basel). 2022 Dec 21;15(1):42. doi: 10.3390/cancers15010042. Cancers (Basel). 2022. PMID: 36612037 Free PMC article. Review.
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.
Polla DL, Farazi Fard MA, Tabatabaei Z, Habibzadeh P, Levchenko OA, Nikuei P, Makrythanasis P, Hussain M, von Hardenberg S, Zeinali S, Fallah MS, Schuurs-Hoeijmakers JHM, Shahzad M, Fatima F, Fatima N, Kaat LD, Bruggenwirth HT, Fleming LR, Condie J, Ploski R, Pollak A, Pilch J, Demina NA, Chukhrova AL, Sergeeva VS, Venselaar H, Masri AT, Hamamy H, Santoni FA, Linda K, Ahmed ZM, Nadif Kasri N, de Brouwer APM, Bergmann AK, Hethey S, Yavarian M, Ansar M, Riazuddin S, Riazuddin S, Silawi M, Ruggeri G, Pirozzi F, Eftekhar E, Taghipour Sheshdeh A, Bahramjahan S, Mirzaa GM, Lavrov AV, Antonarakis SE, Faghihi MA, van Bokhoven H. Polla DL, et al. Among authors: tabatabaei z. Genet Med. 2021 Jul;23(7):1246-1254. doi: 10.1038/s41436-021-01133-w. Epub 2021 Apr 6. Genet Med. 2021. PMID: 33824500 Free PMC article.
Expanding the molecular and clinical phenotypes of FUT8-CDG.
Ng BG, Dastsooz H, Silawi M, Habibzadeh P, Jahan SB, Fard MAF, Halliday BJ, Raymond K, Ruzhnikov MRZ, Tabatabaei Z, Taghipour-Sheshdeh A, Brimble E, Robertson SP, Faghihi MA, Freeze HH. Ng BG, et al. Among authors: tabatabaei z. J Inherit Metab Dis. 2020 Jul;43(4):871-879. doi: 10.1002/jimd.12221. Epub 2020 Feb 23. J Inherit Metab Dis. 2020. PMID: 32049367 Free PMC article.
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