Occupational and Individual Factors Associated with Return to Work in Workers with Multiple Sclerosis von Hosseininejad, Mahin, Kabir-Mokamelkhah, Elaheh, Harirchian, Mohammad Hossein, Sirous, Razieh, Mohammadi, Saber, Kabiri, Samaneh

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Occupational and Individual Factors Associated with Return to Work in Workers with Multiple Sclerosis/Multipl Sklerozlu Iscilerde Ise Donus ile Iliskili Mesleki ve Bireysel Faktorl... von Hosseininejad, Mahin, Kabir-Mokamelkhah, Elaheh, Harirchian, Mohammad Hossein, Sirous, Razieh, Mohammadi, Saber, Kabiri, Samaneh

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Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran von Sharifi, Zohreh, Taheri, Mohammad, Fallah, Mohammad-Sadegh, Abiri, Maryam, Golnabi, Fatemeh, Bagherian, Hamideh, Zeinali, Razieh, Farahzadi, Hossein, Alborji, Marjan, Tehrani, Pardis Ghazizadeh, Amini, Masoume, Asnavandi, Sadaf, Hashemi, Mehrdad, Forouzesh, Flora, Zeinali, Sirous

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Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations von Abiri, Maryam, Saei, Hassan, Eghbali, Maryam, Karamzadeh, Razieh, Shirzadeh, Tina, Sharifi, Zohreh, Zeinali, Sirous

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Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abn... von Vahidnezhad, Hassan, Youssefian, Leila, Saeidian, Amir Hossein, Touati, Andrew, Pajouhanfar, Sara, Baghdadi, Taghi, Shadmehri, Azam Ahmadi, Giunta, Cecilia, Kraenzlin, Marius, Syx, Delfien, Malfait, Fransiska, Has, Cristina, Lwin, Su M., Karamzadeh, Razieh, Liu, Lu, Guy, Alyson, Hamid, Mohammad, Kariminejad, Ariana, Zeinali, Sirous, McGrath, John A., Uitto, Jouni

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Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinit... von Vahidnezhad, Hassan, Youssefian, Leila, Saeidian, Amir Hossein, Zeinali, Sirous, Mansouri, Parvin, Sotoudeh, Soheila, Barzegar, Mohammadreza, Mohammadi-asl, Javad, Karamzadeh, Razieh, Abiri, Maryam, McCormick, Kevin, Fortina, Paolo, Uitto, Jouni

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Inherited Interleukin 2–Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma von Youssefian, Leila, Vahidnezhad, Hassan, Yousefi, Mehdi, Saeidian, Amir Hossein, Azizpour, Arghavan, Touati, Andrew, Nikbakht, Neda, Hesari, Kambiz Kamyab, Adib-Sereshki, Mohammad Mahdi, Zeinali, Sirous, Mansoori, Behzad, Jazayeri, Ali, Karamzadeh, Razieh, Fortina, Paolo, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, Uitto, Jouni

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Librarians’ Participation in the Systematic Reviews Published by Iranian Researchers and Its Impact on the Quality of Reporting Search Strategy von Eskrootchi, Rogheyeh, Shahraki Mohammadi, Azita, Panahi, Sirous, Zahedi, Razieh

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A novel autosomal recessive GJB2‐associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma von Youssefian, Leila, Vahidnezhad, Hassan, Saeidian, Amir Hossein, Mahmoudi, Hamidreza, Karamzadeh, Razieh, Kariminejad, Ariana, Huang, Jianhe, Li, Leping, Jannace, Thomas F., Fortina, Paolo, Zeinali, Sirous, White, Thomas W., Uitto, Jouni

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Molecular Dynamics Simulation of the Consequences of a PYCR1 Mutation (p.Ala189Val) in Patients with Complex Connective Tissue Disorder and Severe Intellectual Disability von Vahidnezhad, Hassan, Karamzadeh, Razieh, Saeidian, Amir Hossein, Youssefian, Leila, Sotoudeh, Soheila, Zeinali, Sirous, Vasei, Mohammad, Golnabi, Fatemeh, Baghdadi, Taghi, Uitto, Jouni

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A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss and palmoplantar keratoderma von Youssefian, Leila, Vahidnezhad, Hassan, Saeidian, Amir Hossein, Mahmoudi, Hamidreza, Karamzadeh, Razieh, Kariminejad, Ariana, Huang, Jianhe, Li, Leping, Jannace, Thomas F., Fortina, Paolo, Zeinali, Sirous, White, Thomas W., Uitto, Jouni

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Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abn... von Vahidnezhad, Hassan, Youssefian, Leila, Saeidian, Amir Hossein, Touati, Andrew, Pajouhanfar, Sara, Baghdadi, Taghi, Shadmehri, Azam Ahmadi, Giunta, Cecilia, Kraenzlin, Marius, Syx, Delfien, Malfait, Fransiska, Has, Cristina, Lwin, Su M, Karamzadeh, Razieh, Liu, Lu, Guy, Alyson, Hamid, Mohammad, Kariminejad, Ariana, Zeinali, Sirous, McGrath, John A, Uitto, Jouni

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In silico analysis of novel mutations in maple syrup urine disease patients from Iran von Abiri, Maryam, Karamzadeh, Razieh, Mojbafan, Marziyeh, Alaei, Mohammad Reza, Jodaki, Atefeh, Safi, Masomeh, Kianfar, Soodeh, Bandehi Sarhaddi, Ameneh, Noori-Daloii, Mohammad Reza, Karimipoor, Morteza, Zeinali, Sirous

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