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Page 1
Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII.
Ebrahimi AH, Bolhassani M, Zarei MR, Heidari M, ArdeshirDavani A, Mehrtash AH, Shiri Z, Heidari M, Soleyman-Nejad M, Taskhiri MH, Norouzbeigi A, Heidari M. Ebrahimi AH, et al. Among authors: mehrtash ah. Arch Iran Med. 2024 Apr 1;27(4):223-226. doi: 10.34172/aim.2024.32. Arch Iran Med. 2024. PMID: 38685849 Free PMC article.
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.
Vaseghi P, Habibi L, Neidich JA, Cao Y, Fattahi N, Rashidi-Nezhad R, Salehnezhad T, Dalili H, Rahimi Sharbaf F, Zarkesh MR, Malekian M, Mokhberdezfuli M, Mehrtash A, Ardeshirdavani A, Kariminejad R, Ghorbansabagh V, Sadeghimoghadam P, Naddaf A, Esmaeilnia Shirvany T, Mosayebi Z, Sahebdel B, Golshahi F, Shirazi M, Shamel S, Moeini R, Heidari A, Daneshmand MA, Ghasemi R, Akrami SM, Rashidi-Nezhad A. Vaseghi P, et al. Among authors: mehrtash a. Eur J Hum Genet. 2024 Oct;32(10):1238-1249. doi: 10.1038/s41431-024-01533-x. Epub 2024 Jan 26. Eur J Hum Genet. 2024. PMID: 38278869
CardioVision: A fully automated deep learning package for medical image segmentation and reconstruction generating digital twins for patients with aortic stenosis.
Rouhollahi A, Willi JN, Haltmeier S, Mehrtash A, Straughan R, Javadikasgari H, Brown J, Itoh A, de la Cruz KI, Aikawa E, Edelman ER, Nezami FR. Rouhollahi A, et al. Among authors: mehrtash a. Comput Med Imaging Graph. 2023 Oct;109:102289. doi: 10.1016/j.compmedimag.2023.102289. Epub 2023 Aug 19. Comput Med Imaging Graph. 2023. PMID: 37633032 Free PMC article.
Deep Learning for Detection and Localization of B-Lines in Lung Ultrasound.
Lucassen RT, Jafari MH, Duggan NM, Jowkar N, Mehrtash A, Fischetti C, Bernier D, Prentice K, Duhaime EP, Jin M, Abolmaesumi P, Heslinga FG, Veta M, Duran-Mendicuti MA, Frisken S, Shyn PB, Golby AJ, Boyer E, Wells WM, Goldsmith AJ, Kapur T. Lucassen RT, et al. Among authors: mehrtash a. IEEE J Biomed Health Inform. 2023 Sep;27(9):4352-4361. doi: 10.1109/JBHI.2023.3282596. Epub 2023 Sep 6. IEEE J Biomed Health Inform. 2023. PMID: 37276107 Free PMC article.
Clinical whole-exome sequencing analysis reveals a novel missense COL11A1 mutation resulting in an 18-week Iranian male aborted fetus with Fibrochondrogenesis 1: A case report.
Mirtavoos-Mahyari H, Ajami S, Mehrtash A, Marashiyan SM, Bahreini F, Sheikhy K, Ghanbari S, Ardeshirdavani A. Mirtavoos-Mahyari H, et al. Among authors: mehrtash a. Clin Case Rep. 2022 Nov 15;10(11):e6574. doi: 10.1002/ccr3.6574. eCollection 2022 Nov. Clin Case Rep. 2022. PMID: 36397853 Free PMC article.
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