Search Results - Foroughmand, A M

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  1. 1
    A preliminary mutation analysis of phenylketonuria in southwest Iran

    A preliminary mutation analysis of phenylketonuria in southwest Iran by Ajami, N, Kazeminezhad, S R, Foroughmand, A M, Hasanpour, M, Aminzadeh, M

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  2. 2
    The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree

    The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree by ADEOKUN, A. M, WEST, S. P, ELLIS, F. R, HALSALL, P. J, HOPKINS, P. M, FOROUGHMAND, A. M, ILES, D. E, ROBINSON, R. L, STEWART, A. D, CURRAN, J. L

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  3. 3
    CytoGTA: A cytoscape plugin for identifying discriminative subnetwork markers using a game theoretic approach

    CytoGTA: A cytoscape plugin for identifying discriminative subnetwork markers using a game theoretic approach by Farahmand, S, Foroughmand-Araabi, M H, Goliaei, S, Razaghi-Moghadam, Z

    Published in PloS one
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  4. 4
    Combination of Epigallocatechin-3-gallate and Silibinin: A Novel Approach for Targeting Both Tumor and Endothelial Cells

    Combination of Epigallocatechin-3-gallate and Silibinin: A Novel Approach for Targeting Both Tumor and Endothelial Cells by Mirzaaghaei, Somaye, Foroughmand, Ali M, Saki, Ghasem, Shafiei, Mohammad

    Published in ACS omega
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  5. 5
    Metal concentrations in cerebrospinal fluid, blood, serum, plasma, hair, and nails in amyotrophic lateral sclerosis: A systematic review and meta-analysis

    Metal concentrations in cerebrospinal fluid, blood, serum, plasma, hair, and nails in amyotrophic lateral sclerosis: A systematic review and meta-analysis by Roos, Per, Kamalian, Aida, Koski, Lassi, Foroughmand, Iman, Darvish, Mahtab, Kamalian, Amirhossein, Fotouhi, Akbar, Razavi, Zahra Emami, Abdi, Siamak, Dehgolan, Shahram Rahimi

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  6. 6
    Metal concentrations in cerebrospinal fluid, blood, serum, plasma, hair, and nails in amyotrophic lateral sclerosis: A systematic review and meta-analysis

    Metal concentrations in cerebrospinal fluid, blood, serum, plasma, hair, and nails in amyotrophic lateral sclerosis: A systematic review and meta-analysis by Kamalian, Aida, Foroughmand, Iman, Koski, Lassi, Darvish, Mahtab, Saghazadeh, Amene, Kamalian, Amirhossein, Razavi, Seyedeh Zahra Emami, Abdi, Siamak, Dehgolan, Shahram Rahimi, Fotouhi, Akbar, Roos, Per M.

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  7. 7
    Effectiveness of telehealth versus in-person care during the COVID-19 pandemic: a systematic review

    Effectiveness of telehealth versus in-person care during the COVID-19 pandemic: a systematic review by Hatef, Elham, Wilson, Renee F., Zhang, Allen, Hannum, Susan M., Kharrazi, Hadi, Davis, Stacey A., Foroughmand, Iman, Weiner, Jonathan P., Robinson, Karen A.

    Published in NPJ digital medicine
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  8. 8
    Development of a Social Risk Score in the Electronic Health Record to Identify Social Needs Among Underserved Populations: Retrospective Study

    Development of a Social Risk Score in the Electronic Health Record to Identify Social Needs Among Underserved Populations: Retrospective Study by Hatef, Elham, Chang, Hsien-Yen, Richards, Thomas M, Kitchen, Christopher, Budaraju, Janya, Foroughmand, Iman, Lasser, Elyse C, Weiner, Jonathan P

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  9. 9
    Application of natural language processing to identify social needs from patient medical notes: development and assessment of a scalable, performant, and rule-based model in an integrated healthcare delivery system

    Application of natural language processing to identify social needs from patient medical notes: development and assessment of a scalable, performant, and rule-based model in an int... by Gray, Geoffrey M, Zirikly, Ayah, Ahumada, Luis M, Rouhizadeh, Masoud, Richards, Thomas, Kitchen, Christopher, Foroughmand, Iman, Hatef, Elham

    Published in JAMIA open
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  10. 10
    Lack of association between the G-660C polymorphism in the dopamine transporter gene (SLC6A3) and schizophrenia in the Iranian population

    Lack of association between the G-660C polymorphism in the dopamine transporter gene (SLC6A3) and schizophrenia in the Iranian population by Foroughmand, Ali M, Galehdari, Hamid, Dastgerdi, Bentalhoda Tirband, Khatami, Saeed Reza, Haidari, Maryam

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  11. 11
    Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran

    Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran by Galehdari, Hamid, Foroughmand, Ali Mohammad, Soorki, Maryam Naderi, Mohammadian, Gholamreza

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  12. 12
    Novel mutation in the EXT-1 gene in an Iranian family affected with hereditary multiple exostoses

    Novel mutation in the EXT-1 gene in an Iranian family affected with hereditary multiple exostoses by Foroughmand, Ali Mohammad, Galehdari, Hamid, Rasouli, Mina, Mohammadian, Gholamreza, Mohammadi, Mansour

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