The association of upper respiratory infections with neuro-radiological course and attack rate of multiple sclerosis: Results from a large prospective cohort von Ghasemi, Moein, Farazandeh, Dorreh, Amini, Behnam, Sedaghat, Mona, Najafi, Anahita, Khayatzadeh Kakhki, Simin, Torabi, Pouya, Jafarimehrabady, Niloofar, Bitaraf, Ali, Shariati, Houria, Gholampour, Golsa, Kazemi, Saminnaz, Naser Moghadasi, Abdorreza, Vajihinejad, Maryam

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Guillain-Barre Syndrome Deterioration After an Abdominal Surgery von Khosroshahi, Nahid, Habibi Zoham, Mojdeh, Khayatzadeh Kakhki, Simin

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Cultural adaptation, validation and standardization of the developmental screening tools ASQ:SE-2 in Iranian children von Shariatpanahi, Ghazal, Kakhki, Simin Khayatzadeh, Pourpashang, Paniz, Ashournia, Parisa, Rahimi, Malihe, Ghasempour, Masoumeh, Ghanbari, Niloufar

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Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation von Karimzadeh, Parvaneh, Khayatzadeh Kakhki, Simin, Esmail Nejad, Shaghayegh Sadat, Houshmand, Masood, Ghofrani, Mohammad

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Pancake Kidney, Rare Kidney Fusion Anomaly in Pediatrics von Yousef Mojtahedi, Sayed, Afshin, Azadeh, Khayatzadeh Kakhki, Simin

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The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy von Mansouri, Vahid, Heidari, Morteza, Bemanalizadeh, Maryam, Azizimalamiri, Reza, Nafissi, Shahriar, Akbari, Masood Ghahvechi, Barzegar, Mohammad, Moayedi, Ali Reza, Badv, Reza Shervin, Mohamadi, Mahmood, Tavasoli, Ali Reza, Amirsalari, Susan, Khajeh, Ali, Inaloo, Soroor, Fatehi, Farzad, Hosseinpour, Sareh, Babaei, Meisam, Hosseini, Seyed Ahmad, Mahdi Hosseiny, Seyyed Mohammad, Fayyazi, Afshin, Hosseini, Firoozeh, Toosi, Mehran Beiraghi, Khosroshahi, Nahid, Ghabeli, Homa, Biglari, Habibeh Nejad, Kakhki, Simin Khayatzadeh, Mirlohi, Seyed Hossein, Bidabadi, Elham, Mohammadi, Bahram, Omrani, Abdolmajid, Sedighi, Mostafa, Vafaee-Shahi, Mohammad, Rasulinezhad, Maryam, Hoseini, Seyyed Mohamad, Movahedinia, Mojtaba, Rezaei, Zahra, Karimi, Parviz, Farshadmoghadam, Hossein, Anvari, Saeed, Yaghini, Omid, Nasiri, Jafar, Zamani, Gholamreza, Ashrafi, Mahmoud Reza

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The clinical features and diagnosis of Metachromatic leukodystrophy: A case series of Iranian Pediatric Patients von Jabbehdari, Sayena, Rahimian, Elham, Jafari, Narjes, Sanii, Sara, Khayatzadehkakhki, Simin, Nejad Biglari, Habibe

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Guillain-Barre Syndrome Deterioration After an Abdominal Surgery von Khosroshahi, Nahid, Habibi Zoham, Mojdeh, Khayatzadeh Kakhki, Simin

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Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation von Karimzadeh, Parvaneh, Khayatzadeh Kakhki, Simin, Esmail Nejad, Shaghayegh Sadat, Houshmand, Masood, Ghofrani, Mohammad

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