Brown adipose tissue transplantation as a novel alternative to obesity treatment: a systematic review von Payab, Moloud, Abedi, Mina, Foroughi Heravani, Najmeh, Hadavandkhani, Mahdieh, Arabi, Maryam, Tayanloo-Beik, Akram, Sheikh Hosseini, Motahareh, Gerami, Hadis, Khatami, Fateme, Larijani, Bagher, Abdollahi, Mohammad, Arjmand, Babak

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Retinitis pigmentosa‐1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation von Neissi, Mostafa, Sheikh‐Hosseini, Motahareh, Mohammadi‐Asl, Javad

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Beneficial effects of cold atmospheric plasma on inflammatory phase of diabetic foot ulcers; a randomized clinical trial von Amini, Mohammad Reza, Sheikh Hosseini, Motahareh, Fatollah, Sara, Mirpour, Shahriar, Ghoranneviss, Mahmoud, Larijani, Bagher, Mohajeri-Tehrani, Mohammad Reza, Khorramizadeh, Mohammad Reza

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Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9 von Neissi, Mostafa, Sheikh‐Hosseini, Motahareh, Mohammadi‐Asl, Misagh, Al‐Badran, Adnan Issa, Roghani, Mojdeh, Mohammadi‐Asl, Javad, Jorfi, Kamele

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Association of Autism Spectrum Disorder in an Iranian Pedigree with a Novel Hereditary Mutation in SETD5 von Hashemipour, Mehdi, Sheikh-Hosseini, Motahareh, Mabudi, Hadideh

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Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene von Neissi, Mostafa, Mohammadi-Asl, Javad, Mohammadi-Asl, Misagh, Roghani, Mojdeh, Sheikh-Hosseini, Motahareh, Issa Al-Badran, Adnan

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A Novel Disease-Causing ASPA Gene Mutation (c.432+1 G>C) in an Iranian Patient with Canavan Disease: A Case Report von Neissi, Mostafa, Sheikh-Hosseini, Motahareh, Mohammadi-Asl, Javad

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Joubert syndrome caused by a TMEM67 mutation: Genotype-phenotype analysis von Neissi, Mostafa, Misagh Mohammadi-Asl, Mojdeh Roghani, Issa Al-Badran, Adnan, Motahareh Sheikh-Hosseini, Mohammadi-Asl, Javad

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A Novel SLC9A6 Mutation Associated with Christianson Syndrome in a Non-Consanguineous Iranian Family: A Case Report von Mehdi Hashemipour, Mostafa Neissi, Mahsa Rashid, Karim Sevari, Motahareh Sheikh-Hosseini, Adnan Issa Al-Badran

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A novel heterozygous TPM2 gene mutation in an Iranian family affected by distal arthrogryposis type 1: a case report von Neissi, Mostafa, Sheikh-Hosseini, Motahareh, Mohammadi-Asl, Javad, Al-Badran, Adnan Issa

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Unveiling a Novel THOC2 Mutation's Role in X-linked Intellectual Disability von Mehdi Hashemipour, Ayad Neissi, Mostafa Neissi, Misagh Mohammadi-Asl, Motahareh Sheikh-Hosseini, Sasan Bavi, Mojdeh Roghani, Javad Mohammadi-Asl

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Clinical and genetic analysis of Niemann-Pick disease type C with a novel NPC1 variant von Neissi, Mostafa, Al-Badran, Adnan Issa, Mohammadi-Asl, Misagh, Al-Badran, Raed Abdulelah, Sheikh-Hosseini, Motahareh, Roghani, Mojdeh, Mohammadi-Asl, Javad

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Homozygous LOXHD1 Nonsense Mutation (c.1787G>A; p.W596X) is Associated with Hearing Loss in an Iranian Family: A Case Report von Neissi, Mostafa, Abdulzahra, Husham, Sheikh-Hosseini, Motahareh, Mabudi, Hadideh, Mohammadi-Asl, Javad, Al-Badran, Raed

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A-Kinase anchor protein 4 (AKAP4) may be considered as a potential early diagnostic breast cancer marker detectable in blood von Sheikh-Hosseini, Motahareh, Salimi, Mahdieh, Mozdarani, Hossein

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Gene Therapy as an Emerging Therapeutic Approach to Breast Cancer: New Developments and Challenges von Sheikh-Hosseini, Motahareh, Larijani, Bagher, Gholipoor Kakroodi, Zahra, Shokoohi, Mahshid, Moarefzadeh, Mohammad, Sayahpour, Forough Azam, Goodarzi, Parisa, Arjmand, Babak

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GMP-Compliant Adenoviral Vectors for Gene Therapy von Arjmand, Babak, Alavi-Moghadam, Sepideh, Payab, Moloud, Goodarzi, Parisa, Sheikh Hosseini, Motahareh, Tayanloo-Beik, Akram, Rezaei-Tavirani, Mostafa, Larijani, Bagher

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Mesenchymal stem cells’ seeded amniotic membrane as a tissue-engineered dressing for wound healing von Aghayan, Hamid Reza, Hosseini, Motahareh Sheikh, Gholami, Mahdi, Mohamadi-jahani, Fereshteh, Tayanloo-Beik, Akram, Alavi-Moghadam, Sepideh, Payab, Moloud, Goodarzi, Parisa, Abdollahi, Mohammad, Larijani, Bagher, Arjmand, Babak

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Birjand longitudinal aging study (BLAS): the objectives, study protocol and design (wave I: baseline data gathering) von Moodi, Mitra, Firoozabadi, Mohammad Dehghani, Kazemi, Tooba, Payab, Moloud, Ghaemi, Kazem, Miri, Mohammad Reza, Sharifzadeh, Gholamreza, Fakhrzadeh, Hosein, Ebrahimpur, Mahbube, Arzaghi, Seyed Masoud, Zarban, Asghar, Mirimoghadam, Ebrahim, Sharifi, Ali, Hosseini, Motahareh Sheikh, Esmaeili, Aliakbar, Mohammadifard, Mahyar, Ehsanbakhsh, Alireza, Ahmadi, Zahra, Yaghoobi, Gholam Hossain, Hosseinirad, Seyed Abbas, Davari, Mohamad Hossein, Heydari, Behroz, Nikandish, Malihe, Norouzpour, Amir, Naseri, Saeed, Khorashadizadeh, Masoumeh, Mohtashami, Somayeh, Mehdizadeh, Kambiz, Ahmadi, Galileh, Soltani, Huriye, Khodbakhshi, Huriye, Sharifi, Farshad, Larijan, Bagher

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Birjand longitudinal aging study von Moodi, Mitra, Firoozabadi, Mohammad Dehghani, Kazemi, Tooba, Payab, Moloud, Ghaemi, Kazem, Miri, Mohammad Reza, Sharifzadeh, Gholamreza, Fakhrzadeh, Hosein, Ebrahimpur, Mahbube, Arzaghi, Seyed Masoud, Zarban, Asghar, Mirimoghadam, Ebrahim, Sharifi, Ali, Hosseini, Motahareh Sheikh, Esmaeili, Aliakbar, Mohammadifard, Mahyar, Ehsanbakhsh, Alireza, Ahmadi, Zahra, Yaghoobi, Gholam Hossain, Hosseinirad, Seyed Abbas, Davari, Mohamad Hossein, Heydari, Behroz, Nikandish, Malihe, Norouzpour, Amir, Naseri, Saeed, Khorashadizadeh, Masoumeh, Mohtashami, Somayeh, Mehdizadeh, Kambiz, Ahmadi, Galileh, Soltani, Huriye, Khodbakhshi, Huriye, Sharifi, Farshad, Larijan, Bagher

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Retinitis pigmentosa-1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation von Neissi, Mostafa, Sheikh-Hosseini, Motahareh, Mohammadi-Asl, Javad

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