Search Results - Farajzadeh Valilou, Saeed

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  1. 1
    PD‐1/PD‐L1 pathway: Basic biology and role in cancer immunotherapy

    PD‐1/PD‐L1 pathway: Basic biology and role in cancer immunotherapy by Salmaninejad, Arash, Valilou, Saeed Farajzadeh, Shabgah, Arezoo Gowhari, Aslani, Saeed, Alimardani, Malihe, Pasdar, Alireza, Sahebkar, Amirhossein

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  2. 2
    The role of inflammatory cytokines and tumor associated macrophages (TAMs) in microenvironment of pancreatic cancer

    The role of inflammatory cytokines and tumor associated macrophages (TAMs) in microenvironment of pancreatic cancer by Farajzadeh Valilou, Saeed, Keshavarz-Fathi, Mahsa, Silvestris, Nicola, Argentiero, Antonella, Rezaei, Nima

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  3. 3
    Tumor-associated macrophages: role in cancer development and therapeutic implications

    Tumor-associated macrophages: role in cancer development and therapeutic implications by Salmaninejad, Arash, Valilou, Saeed Farajzadeh, Soltani, Arash, Ahmadi, Sepideh, Abarghan, Yousef Jafari, Rosengren, Rhonda J., Sahebkar, Amirhossein

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  4. 4
    A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy

    A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy by Farajzadeh Valilou, Saeed, Karimzad Hagh, Javad, Salimi Asl, Mohammad, Abdi Rad, Isa, Edizadeh, Masoud, Pooladi, Arash

    Published in Clinical case reports
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  5. 5
    Eighth case of Li‐Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype

    Eighth case of Li‐Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype by Edizadeh, Masoud, Kaymakcalan, Hande, Valilou, Saeed Farajzadeh, Şahin, Yavuz

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  6. 6
    Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems

    Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems by Farajzadeh Valilou, Saeed, Alavi, Afagh, Pashaei, Mahdiyeh, Ghasemi Firouzabadi, Saghar, Shafeghati, Yousef, Nozari, Ahoura, Hadipour, Fatemeh, Hadipour, Zahra, Maghsoodlou Estrabadi, Bijan, Gholamreza Noorazar, Seyed, Banihashemi, Susan, Karimian, Javad, Fattahi, Mahshid, Behjati, Farkhondeh

    Published in Molecular syndromology
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  7. 7
    Duchenne muscular dystrophy: an updated review of common available therapies

    Duchenne muscular dystrophy: an updated review of common available therapies by Salmaninejad, Arash, Valilou, Saeed Farajzadeh, Bayat, Hadi, Ebadi, Nader, Daraei, Abdolreza, Yousefi, Meysam, Nesaei, Abolfazl, Mojarrad, Majid

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  8. 8
    PTPN22 Gene Polymorphisms in Pediatric Systemic Lupus Erythematosus

    PTPN22 Gene Polymorphisms in Pediatric Systemic Lupus Erythematosus by Bahrami, Tayyeb, Valilou, Saeed Farajzadeh, Sadr, Maryam, Soltani, Samaneh, Salmaninejad, Arash, Soltaninejad, Ehsan, Yekaninejad, Mir Saeed, Ziaee, Vahid, Rezaei, Nima

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  9. 9
    First Report of Congenital Short Bowel Syndrome in an Iranian Patient Caused by a Mutation in the CLMP Gene

    First Report of Congenital Short Bowel Syndrome in an Iranian Patient Caused by a Mutation in the CLMP Gene by Gharesouran, Jalal, Esfahani, Behnaz Salek, Valilou, Saeed Farajzadeh, Moradi, Mohsen, Mousavi, Mir Hadi, Rezazadeh, Maryam

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  10. 10
    Eighth case of Li-Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype

    Eighth case of Li-Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype by Edizadeh, Masoud, Kaymakcalan, Hande, Valilou, Saeed Farajzadeh, Şahin, Yavuz

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  11. 11
    A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy

    A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy by Farajzadeh Valilou, Saeed, Karimzad Hagh, Javad, Salimi Asl, Mohammad, Abdi Rad, Isa, Edizadeh, Masoud, Pooladi, Arash

    Published in Clinical case reports
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  12. 12
    First Report of Congenital Short Bowel Syndrome in an Iranian Patient Caused by a Mutation in the CLMP Gene

    First Report of Congenital Short Bowel Syndrome in an Iranian Patient Caused by a Mutation in the CLMP Gene by Gharesouran, Jalal, Esfahani, Behnaz Salek, Valilou, Saeed Farajzadeh, Moradi, Mohsen, Mousavi, Mir Hadi, Rezazadeh, Maryam

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