Gene therapy approaches for GM1 gangliosidosis: Focus on animal and cellular studies von Hosseini, Kamran, Fallahi, Jafar, Tabei, Seyed M. B., Razban, Vahid

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The effect of N-acetyl cysteine consumption on men with abnormal sperm parameters due to positive history of COVID-19 in the last three months von Rafiee, Bahare, Bagher Tabei, Seyed Mohammad

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MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family von Zeraatpisheh, Zahra, Sichani, Ali Saber, Kamal, Neda, Khamirani, Hossein Jafari, Zoghi, Sina, Ehsani, Elham, Mohammadi, Sanaz, Tabei, Seyed Sajjad, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher, Dianatpour, Mehdi

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Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1 von Faghihi, Fatemeh, Khamirani, Hossein Jafari, Zoghi, Sina, Kamal, Neda, Yeganeh, Babak Shirazi, Dianatpour, Mehdi, Bagher Tabei, Seyed Mohammad, Dastgheib, Seyed Alireza

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The effects of melatonin and metformin on histological characteristics of the ovary and uterus in letrozole-induced polycystic ovarian syndrome mice: A stereological study von Lohrasbi, Parvin, Karbalay-Doust, Saied, Mohammad Bagher Tabei, Seyed, Azarpira, Negar, Alaee, Sanaz, Rafiee, Bahare, Bahmanpour, Soghra

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Phenotype of ST3GAL3 deficient patients: A case and review of the literature von Khamirani, Hossein Jafari, Zoghi, Sina, Faghihi, Fatemeh, Dastgheib, Seyed Alireza, Hassanipour, Hamidreza, Bagher Tabei, Seyed Mohammad, Mohammadi, Sanaz, Masoudi, Marjan, Poorang, Shiva, Ehsani, Elham, Dianatpour, Mehdi

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A combination of two novels homozygous FCSK variants cause disorder of glycosylation with defective fucosylation: New patient and literature review von Manoochehri, Jamal, Kamal, Neda, Khamirani, Hossein Jafari, Zoghi, Sina, Haghighi, Maryam Fazelzadeh, Goodarzi, Hamed Reza, Bagher Tabei, Seyed Mohammad

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Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder von Mohammadi, Sanaz, Jafari Khamirani, Hossein, Zoghi, Sina, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher, Talebzadeh, Mahdieh, Adibi, Mohammad Hossein, Dianatpour, Mehdi

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Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS von Khamirani, Hossein Jafari, Zoghi, Sina, Sichani, Ali Saber, Dianatpour, Mehdi, Mohammadi, Sanaz, Tabei, Seyed Mohammad Bagher, Dastgheib, Seyed Alireza

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Designing a "near-death experience" reality testing system von Shakeri, Ali, Ebrahimi, Sedigheh, Jahromi, Mohsen, Tabei, Seyed

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Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1 von Alavi, Omid, Khamirani, Hossein Jafari, Zoghi, Sina, Feili, Afrooz, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher, Manoochehri, Jamal, Panahandeh, Seyed Mehdi, Kamali, Majid, Dianatpour, Mehdi

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Creating cell and animal models of human disease by genome editing using CRISPR/Cas9 von Zarei, Ali, Razban, Vahid, Hosseini, Seyed Ebrahim, Tabei, Seyed Mohammad Bagher

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EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review von Abbasi, Zahra, Jafari Khamirani, Hossein, Tabei, Seyed Mohammad Bagher, Manoochehri, Jamal, Dianatpour, Mehdi, Dastgheib, Seyed Alireza

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Modalization and Transcendence of Health in the Coming Decade: Emphasizing the Human Cognitive System in the Stories of Prophets in the Holy Quran von Tabei, Seyed Ziaeddin, Khiveh, Fatemeh, Ebrahimi, Sedigheh

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A novel PTRH2 missense mutation causing IMNEPD: a case report von Khamirani, Hossein Jafari, Zoghi, Sina, Dianatpour, Mehdi, Jankhah, Aria, Tabei, Seyed Sajjad, Mohammadi, Sanaz, Dastgheib, Seyed Alireza

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An unsigned truncated sequential multiplier with variable error compensation von Tabei, Seyed Mohammad M., Nikmehr, Hooman

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EXOSC9 mutation causes pontocerebellar hypoplasia type 1D (PCH1D): Refining the phenotype and literature review von Khamirani, Hossein Jafari, Sichani, Ali Saber, Panahandeh, Seyed Mehdi, Zoghi, Sina, Tabei, Seyed Sajjad, Darayee, Maryam, Talebzadeh, Mahdieh, Dianatpour, Mehdi, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher

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Exosome as a target for cancer treatment von Nafar, Samira, Nouri, Negar, Alipour, Maedeh, Fallahi, Jafar, Zare, Fateme, Tabei, Seyed Mohammad Bagher

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A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report von Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi

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Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report von Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi

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