In vitro cytotoxicity of Cuminum cyminum essential oil loaded SLN nanoparticle von Masoud Tavasoli, Maryam Tatari, Maliheh Samadi Kazemi, Seyedeh Faezeh Taghizadeh

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Identification of novel loss of function variants in MBOAT7 resulting in intellectual disability von Heidari, Erfan, Caddeo, Andrea, Zarabadi, Kiana, Masoudi, Maryam, Tavasoli, Ali Reza, Romeo, Stefano, Garshasbi, Masoud

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Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum von Heidari, Erfan, Harrison, Alexander N., Jafarinia, Ehsan, Tavasoli, Ali Reza, Almadani, Navid, Molday, Robert S., Garshasbi, Masoud

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Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy von Heidari, Erfan, Rasoulinezhad, Maryam, Pak, Neda, Reza Ashrafi, Mahmoud, Heidari, Morteza, Banwell, Brenda, Garshasbi, Masoud, Reza Tavasoli, Ali

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Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report von Zardadi, Safoura, Razmara, Ehsan, Rasoulinezhad, Maryam, Babaei, Meisam, Ashrafi, Mohammad Reza, Pak, Neda, Garshasbi, Masoud, Tavasoli, Ali Reza

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Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case report von Aryan, Hajar, Razmara, Ehsan, Farhud, Dariush, Zarif-Yeganeh, Marjan, Zokaei, Shaghayegh, Hassani, Seyed Abbas, Ashrafi, Mahmoud Reza, Garshasbi, Masoud, Tavasoli, Ali Reza

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Identification of a Novel Homozygous GLS Gene Variant Associated with Developmental and Epileptic Encephalopathy (DEE) Type 71 von Bazgir, Afsaneh, Agha Gholizadeh, Mehdi, Kahani, Seyyed Mohammad, Tavasoli, Ali Reza, Garshasbi, Masoud

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Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients von Dehnavi, Ali Zare, Bemanalizadeh, Maryam, Kahani, Seyyed Mohammad, Ashrafi, Mahmoud Reza, Rohani, Mohammad, Toosi, Mehran Beiraghi, Heidari, Morteza, Hosseinpour, Sareh, Amini, Behnam, Zokaei, Shaghayegh, Rezaei, Zahra, Aryan, Hajar, Amanat, Man, Vahidnezhad, Hassan, Mohammadi, Pouria, Garshasbi, Masoud, Tavasoli, Ali Reza

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Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients von Dehnavi, Ali Zare, Bemanalizadeh, Maryam, Kahani, Seyyed Mohammad, Ashrafi, Mahmoud Reza, Rohani, Mohammad, Toosi, Mehran Beiraghi, Heidari, Morteza, Hosseinpour, Sareh, Amini, Behnam, Zokaei, Shaghayegh, Rezaei, Zahra, Aryan, Hajar, Amanat, Man, Vahidnezhad, Hassan, Mohammadi, Pouria, Garshasbi, Masoud, Tavasoli, Ali Reza

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Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian families von Ashrafi, Mahmoud Reza, Dehnavi, Ali Zare, Tavasoli, Ali Reza, Heidari, Morteza, Ghahvechi Akbari, Masoud, Ronagh, Ali Reza, Ghafouri, Mohammad, Mahdieh, Nejat, Mohammadi, Pouria, Rezaei, Zahra

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Association of intestinal oxalate‐degrading bacteria with recurrent calcium kidney stone formation and hyperoxaluria: a case–control study von Tavasoli, Sanaz, Alebouyeh, Masoud, Naji, Mohammad, Shakiba majd, Ghazaleh, Shabani Nashtaei, Maryam, Broumandnia, Nasrin, Basiri, Abbas

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RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant von Kameli, Reyhaneh, Amanat, Man, Rezaei, Zahra, Hosseionpour, Sareh, Nikbakht, Sedigheh, Alizadeh, Houman, Ashrafi, Mahmoud Reza, Omrani, Abdolmajid, Garshasbi, Masoud, Tavasoli, Ali Reza

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Evaluation of Serum and Salivary Interleukin-6 and Interleukin-8 Levels in Oral Squamous Cell Carcinoma Patients: Systematic Review and Meta-Analysis von Rezaei, Farzad, Mozaffari, Hamid Reza, Tavasoli, Jafar, Zavattaro, Elisa, Imani, Mohammad Moslem, Sadeghi, Masoud

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Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1: a case report von Khalesi, Raziyeh, Razmara, Ehsan, Asgaritarghi, Golareh, Tavasoli, Ali Reza, Riazalhosseini, Yasser, Auld, Daniel, Garshasbi, Masoud

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Death Causes Among Iranian Children With Leukodystrophies von Shiva, Mahsa, Hosseinpour, Sareh, Ashrafi, Mahmoud Reza, Heidari, Morteza, Rezaei, Zahra, Zebardast, Jayran, Mohammadpour, Masoud, Bonkowsky, Joshua L, Tavasoli, Ali Reza

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Efficacy and safety of miglustat in the treatment of GM2 gangliosidosis: A systematic review von Mansouri, Vahid, Tavasoli, Ali Reza, Khodarahmi, Masoud, Dakkali, Mohammad Sedigh, Daneshfar, Sara, Ashrafi, Mahmoud Reza, Heidari, Morteza, Hosseinpour, Sareh, Sharifianjazi, Fariborz, Bemanalizadeh, Maryam

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Homozygous in‐frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family von Heidari, Erfan, Razmara, Ehsan, Hosseinpour, Sareh, Tavasoli, Ali Reza, Garshasbi, Masoud

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Gas Separation Polysulfone Membranes Modified by Cadmium-based Nanoparticles von Tavasoli, Elmira, Sadeghi, Morteza, Riazi, Hossein, Shamsabadi, Ahmad Arabi, Soroush, Masoud

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A novel missense variant in the LMNB2 gene causes progressive myoclonus epilepsy von Soleimanipour, Fardin, Razmara, Ehsan, Rahbarizadeh, Fatemeh, Fallahi, Elnaz, Khodaeian, Mehrnoosh, Tavasoli, Ali Reza, Garshasbi, Masoud

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The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population von Mahdieh, Nejat, Heidari, Morteza, Rezaei, Zahra, Tavasoli, Ali Reza, Hosseinpour, Sareh, Rasulinejad, Maryam, Dehnavi, Ali Zare, Ghahvechi Akbari, Masoud, Badv, Reza Shervin, Vafaei, Elahe, Mohebbi, Ali, Mohammadi, Pouria, Hosseiny, Seyyed Mohammad Mahdi, Azizimalamiri, Reza, Nikkhah, Ali, Pourbakhtyaran, Elham, Rohani, Mohammad, Khanbanha, Narges, Nikbakht, Sedigheh, Movahedinia, Mojtaba, Karimi, Parviz, Ghabeli, Homa, Hosseini, Seyed Ahmad, Rashidi, Fatemeh Sadat, Garshasbi, Masoud, Kashani, Morteza Rezvani, Ghiasvand, Noor M, Zuchner, Stephan, Synofzik, Matthis, Ashrafi, Mahmoud Reza

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