Genotype–phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients von Erfanian Omidvar, Maryam, Torkamandi, Shahram, Rezaei, Somaye, Alipoor, Behnam, Omrani, Mir Davood, Darvish, Hossein, Ghaedi, Hamid

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Stability and release kinetics of nanoliposomes containing bitter melon fruit extract at different temperatures and pH values, and in simulated gastrointestinal conditions von Raftani Amiri, Zeynab, Rezaei Erami, Somaye, Jafari, Seid Mahdi, Ahmadian, Soheila

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Physicochemical properties of yogurt enriched with nanoliposomes containing bitter melon extract von Raftani Amiri, Zeynab, Rezaei Erami, Somaye, Jafari, Seid Mahdi, Ahmadian, Soheila

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Dysregulation of long noncoding RNA MEG3 and NLRC5 expressions in patients with relapsing-remitting multiple sclerosis: is there any correlation? von Torkamandi, Shahram, Bahrami, Shima, Ghorashi, Tahereh, Dehani, Mohammad, Bayat, Hadi, Hoseini, Seyyed Mohamad, Rezaei, Somaye, Soosanabadi, Mohsen

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Nanoliposomal encapsulation of Bitter Gourd (Momordica charantia) fruit extract as a rich source of health-promoting bioactive compounds von Rezaei Erami, Somaye, Raftani Amiri, Zeynab, Jafari, Seid Mahdi

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The novel homozygous p.Asn197_Ser201del mutation in BTD gene is associated with profound biotinidase deficiency in an Iranian consanguineous family von Torkamandi, Shahram, Rezaei, Somaye, Mirfakhraie, Reza, Golmohamadi, Sara, Gholami, Milad

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Barite Replacement as a Key Factor in the Genesis of Sediment-Hosted Zn-Pb±Ba and Barite-Sulfide Deposits: Ore Fluids and Isotope (S and Sr) Signatures from Sediment-Hosted Zn-Pb±B... von Rajabi, Abdorrahman, Mahmoodi, Pouria, Alfonso, Pura, Canet, Carles, Andrew, Colin, Azhdari, Saeideh, Rezaei, Somaye, Alaminia, Zahra, Tamarzadeh, Somaye, Yarmohammadi, Ali, Khan Mohammadi, Ghazaleh, Saeidi, Rasoul

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Reactive arthritis after Gam-COVID-Vac vaccination: A case report von Shokraee, Kamyar, Rezaei, Somaye Sadat, Shahriarian, Shahriar, Masoumi, Maryam, Parsaei, Amirhossein, Amini, Behnam

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Mineralization and Structural Controls of the AB-Bid Carbonate-Hosted Pb-Zn (±Cu) Deposit, Tabas-Posht e Badam Metallogenic Belt, Iran von Rajabi, Abdorrahman, Canet, Carles, Alfonso, Pura, Mahmoodi, Pouria, Yarmohammadi, Ali, Sharifi, Shahba, Mahdavi, Amir, Rezaei, Somaye

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Isolated intracranial Rosai-Dorfman disease in an adult man: Report of a rare case von Rezaei, Somaye, Zarzanalivan, Fariba, Pirouti, Pouya, Amiri Nikpour, Mohammad Reza, Javadi, Abdolreza, Torkamandi, Shahram

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Sarcoidosis with multiple organ involvement and uncommon symptoms: A case report von Khalaji, Amirmohammad, Rezaei, Somaye Sadat, Shajari, Rasoul, Masoumi, Maryam

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Ventricular and atrial function assessment with transthoracic echocardiography in patients with rheumatic inflammatory disease von Norouzi, Somayyeh, Khalaji, Amirmohammad, Namazi, Mansoor, Rezaei, Somaye Sadat, Behnoush, Amir Hossein, Masoumi, Maryam

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COVID-19 in Patients with Rheumatic Disease Using Immunomodulatory Drugs: Imaging Findings and Predictors of Hospitalization von Azizi, Hossein, Karimi, Hanie, Kazemi, Mahdi, Rezaei, Somaye Sadat, Parsaei, Amirhossein, Aghaali, Mohammad, Vafaeimanesh, Jamshid, Torabi, Pouya, Amini, Behnam, Masoumi, Maryam

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Comparative Study of PRMT1 and MAPK14 Genes Expression in Healthy and Oligospermic Individuals von Somaye Rezaei, Maryam Khoshsokhan-Mozaffar, Naser Kalhor

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Gut microbiome and multiple sclerosis: New insights and perspective von Esmaeil Amini, Mohammad, Shomali, Navid, Bakhshi, Arash, Rezaei, Somaye, Hemmatzadeh, Maryam, Hosseinzadeh, Ramin, Eslami, Solat, Babaie, Farhad, Aslani, Saeed, Torkamandi, Shahram, Mohammadi, Hamed

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Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome von Torkamandi, Shahram, Rezaei, Somaye, Mirfakhraei, Reza, Askari, Masomeh, Piltan, Samira, Gholami, Milad

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Arts Education in Iran: An Interview with Khosrow Bagheri Noaparast von Rezaei, Somaye

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A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity) von Torkamandi, Shahram, Rezaei, Somaye, Mirfakhraie, Reza, Bayat, Sahar, Piltan, Samira, Gholami, Milad

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Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss von Torkamandi, Shahram, Bayat, Sahar, Mirfakhraie, Reza, Rezaei, Somaye, Askari, Masomeh, Piltan, Samira, Gholami, Milad

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COVID-19 in Patients with Rheumatic Disease Using Immunomodulatory Drugs: Imaging Findings and Predictors of Hospitalization von Azizi, Hossein, Karimi, Hanie, Kazemi, Mahdi, Rezaei, Somaye Sadat, Parsaei, Amirhossein, Aghaali, Mohammad, Vafaeimanesh, Jamshid, Torabi, Pouya, Amini, Behnam, Masoumi, Maryam

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