Hasil Pencarian - Mohammad hasan Mohammadi

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  1. 1
    Model of managing challenges facing banking system in sanction

    Model of managing challenges facing banking system in sanction oleh Hossein Ghazaavi, Mohammad hasan Mohammadi

    Diterbitkan 2015-09-01
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  2. 2
    The use of magnetic resonance imaging to study the brain size of young children with autism

    The use of magnetic resonance imaging to study the brain size of young children with autism oleh Farah Ashrafzadeh, Mehran Beiraghi Toosi, Mohammad Hasan Mohammadi

    Diterbitkan 2016-07-01
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  3. 3
    Protective Effects of Ursodeoxycholic Acid on Valproic Acid Induced Hepatotoxicity in Epileptic Children with Recurrent Seizure; A Double-Blinded Randomized Clinical Trial

    Protective Effects of Ursodeoxycholic Acid on Valproic Acid Induced Hepatotoxicity in Epileptic Children with Recurrent Seizure; A Double-Blinded Randomized Clinical Trial oleh Iraj Shahramian, Ali Bazi, Rosa Mostafaee, Mohammad Hasan Mohammadi

    Diterbitkan 2020-03-01
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  4. 4
    Assessment of scaling and corrosion potential of drinking water resources of Iranshahr

    Assessment of scaling and corrosion potential of drinking water resources of Iranshahr oleh Mahmoud Taghavi, Mohammad Hasan Mohammadi, Majid Radfard, Yadolah Fakhri, Safoura Javan

    Diterbitkan 2019-01-01
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  5. 5
    PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy

    PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy oleh Hormos Salimi Dafsari, Joshua G. Pemberton, Elizabeth A. Ferrer, Tony Yammine, Chantal Farra, Mohammad Hasan Mohammadi, Ehsan Ghayoor Karimiani, Narges Hashemi, Mirna Souaid, Sandra Sabbagh, Paria Najarzadeh Torbati, Suliman Khan, Emmanuel Roze, Andres Moreno‐De‐Luca, Aida M. Bertoli‐Avella, Henry Houlden, Tamas Balla, Reza Maroofian

    Diterbitkan 2022-09-01
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  6. 6
    Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

    Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders oleh Paola Borgia, Simona Baldassari, Nicoletta Pedemonte, Ebba Alkhunaizi, Gianluca D’Onofrio, Domenico Tortora, Elisa Calì, Paolo Scudieri, Ganna Balagura, Ilaria Musante, Maria Cristina Diana, Marina Pedemonte, Maria Stella Vari, Michele Iacomino, Antonella Riva, Roberto Chimenz, Giuseppe D. Mangano, Mohammad Hasan Mohammadi, Mehran Beiraghi Toosi, Farah Ashrafzadeh, Shima Imannezhad, Ehsan Ghayoor Karimiani, Andrea Accogli, Maria Cristina Schiaffino, Mohamad Maghnie, Miguel Angel Soler, Karl Echiverri, Charles K. Abrams, Pasquale Striano, Sara Fortuna, Reza Maroofian, Henry Houlden, Federico Zara, Chiara Fiorillo, Vincenzo Salpietro

    Diterbitkan 2022-07-01
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  7. 7
    Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity

    Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity oleh Sheng-Jia Lin, Barbara Vona, Tracy Lau, Kevin Huang, Maha S. Zaki, Huda Shujaa Aldeen, Ehsan Ghayoor Karimiani, Clarissa Rocca, Mahmoud M. Noureldeen, Ahmed K. Saad, Cassidy Petree, Tobias Bartolomaeus, Rami Abou Jamra, Giovanni Zifarelli, Aditi Gotkhindikar, Ingrid M. Wentzensen, Mingjuan Liao, Emalyn Elise Cork, Pratishtha Varshney, Narges Hashemi, Mohammad Hasan Mohammadi, Aboulfazl Rad, Juanita Neira, Mehran Beiraghi Toosi, Cordula Knopp, Ingo Kurth, Thomas D. Challman, Rebecca Smith, Asmahan Abdalla, Thomas Haaf, Mohnish Suri, Manali Joshi, Wendy K. Chung, Andres Moreno-De-Luca, Henry Houlden, Reza Maroofian, Gaurav K. Varshney

    Diterbitkan 2023-11-01
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