Hasil Pencarian - Maryam Sedghi

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  1. 1
    Neurodevelopmental Outcome of Patients With Agenesis of Corpus Callosum

    Neurodevelopmental Outcome of Patients With Agenesis of Corpus Callosum oleh Maryam Sedghi, Mohammad Hossein Hemat

    Diterbitkan 2021-04-01
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  2. 2
    Clinical Importance of Pericentric Inversion of Chromosome 9: A Case Report of Miscarriage and Neonatal Death

    Clinical Importance of Pericentric Inversion of Chromosome 9: A Case Report of Miscarriage and Neonatal Death oleh Nayereh Nouri, narges nouri, Maryam Sedghi

    Diterbitkan 2011-04-01
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  3. 3
    Comparison of the effectiveness of couple therapy methods in the theory of Choice, acceptance and commitment (ACT), and integrative couple therapy in marital commitment of couples

    Comparison of the effectiveness of couple therapy methods in the theory of Choice, acceptance and commitment (ACT), and integrative couple therapy in marital commitment of couples oleh Maryam Sedghi, Azra Ghaffari, Reza Kazemi, Mohammad Narimani

    Diterbitkan 2019-12-01
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  4. 4
    How realistic is static traffic assignment? Analyzing automatic number-plate recognition data and image processing of real-time traffic maps for investigation

    How realistic is static traffic assignment? Analyzing automatic number-plate recognition data and image processing of real-time traffic maps for investigation oleh Hamid Mirzahossein, Iman Gholampour, Maryam Sedghi, Lei Zhu

    Diterbitkan 2021-03-01
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  5. 5
    Total graph of a $0$-distributive lattice

    Total graph of a $0$-distributive lattice oleh Shahabaddin Ebrahimi Atani, Saboura Dolati Pishhesari, Mehdi Khoramdel, Maryam Sedghi

    Diterbitkan 2018-07-01
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  6. 6
    Effects of early versus delayed excision and grafting on the return of the burned hand function

    Effects of early versus delayed excision and grafting on the return of the burned hand function oleh Seyed Hamid Salehi, Mohammad Javad Fatemi, Maryam Sedghi, Mitra Niazi

    Diterbitkan 2016-01-01
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  7. 7
    A case report of 22q11 deletion syndrome confirmed by array-CGH method

    A case report of 22q11 deletion syndrome confirmed by array-CGH method oleh Maryam Sedghi, Narges Nouri, Hossein Abdali, Mehrdad Memarzadeh, Nayereh Nouri

    Diterbitkan 2012-01-01
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  8. 8
    An insight into genetics of non-syndromic cleft palate

    An insight into genetics of non-syndromic cleft palate oleh Nayereh Nouri, Padideh Karimi, Salehi Mansoor, Mehrdad Memarzadeh, Hamid Ganji, Maryam Sedghi

    Diterbitkan 2013-01-01
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  9. 9
    A novel missense mutation in the GNE gene in an Iranian patient with hereditary inclusion body myopathy

    A novel missense mutation in the GNE gene in an Iranian patient with hereditary inclusion body myopathy oleh Mahdiyeh Behnam, Shin Jin-Hong, Dae-Seong Kim, Keivan Basiri, Yalda Nilipour, Maryam Sedghi

    Diterbitkan 2014-01-01
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  10. 10
    Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset

    Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an I... oleh Nayereh Nouri, Esmat Fazel-Najafabadi, Mansoor Salehi, Majid Hosseinzadeh, Mahdieh Behnam, Mohammad Reza Ghazavi, Maryam Sedghi

    Diterbitkan 2014-01-01
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  11. 11
    Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran

    Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran oleh Maryam Sedghi, Mahdiyeh Behnam, Esmat Fazel, Mansoor Salehi, Hamid Ganji, Rokhsareh Meamar, Majid Hosseinzadeh, Nayereh Nouri

    Diterbitkan 2014-01-01
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  12. 12
    Evaluation of neural gene expression in serum treated embryonic stem cells in Alzheimer′s patients

    Evaluation of neural gene expression in serum treated embryonic stem cells in Alzheimer′s patients oleh Leila Dehghani, Batool Hashemi-Beni, Elahe Poorazizi, Fariborz Khorvash, Vahid Shaygannejad, Maryam Sedghi, Sahar Vesal, Rokhsareh Meamar

    Diterbitkan 2013-01-01
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  13. 13
    Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants

    Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants oleh Hamidreza Mianesaz, Safoura Ghalamkari, Mansoor Salehi, Mahdiyeh Behnam, Majid Hosseinzadeh, Keivan Basiri, Majid Ghasemi, Maryam Sedghi, Behnaz Ansari

    Diterbitkan 2023-02-01
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  14. 14
    Evaluation of the Coronary Angiography Results in Patients Referred to Cardiac Centers in Isfahan City, Iran

    Evaluation of the Coronary Angiography Results in Patients Referred to Cardiac Centers in Isfahan City, Iran oleh Maryam Sedghi, Seyed Mohammad Hashemi, Alireza Khosravi, Ahmad Reza Riaziat, Mohammad Reza Rezayatmand, Vahid Sabetjoo, Hamed Tasdighi, Mojtaba Baktashian

    Diterbitkan 2017-04-01
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  15. 15
    Study of prenatal screening tests in pregnant women and comparison with fetal karyotype results

    Study of prenatal screening tests in pregnant women and comparison with fetal karyotype results oleh Mojtaba Baktashian, Maryam Sedghi, Mansour Salehi, Fateme sadat Mirlohi, Elahe Zarean, Atefe Baghersad, Sadegh Valian, Rasoul Saraian, Majid Hoseinzade

    Diterbitkan 2018-01-01
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  16. 16
    Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families

    Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families oleh Maryam Sedghi, Elham Esfandiari, Esmat Fazel-Najafabadi, Mansoor Salehi, Abbas Salavaty, Shirin Fattahpour, Leila Dehghani, Nayerossadat Nouri, Fariborz Mokarian

    Diterbitkan 2016-01-01
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  17. 17
    Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study

    Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study oleh Maryam Sedghi, Ali‐Reza Moslemi, Montse Olive, Masoud Etemadifar, Behnaz Ansari, Jafar Nasiri, Leila Emrahi, Hamid‐Reza Mianesaz, Nigel G. Laing, Homa Tajsharghi

    Diterbitkan 2019-11-01
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  18. 18
    Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes

    Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes oleh Hamidreza Mianesaz, Safoura Ghalamkari, Farzaneh Abbasi, Maryam Razzaghy‐Azar, Fatemeh Sayarifard, Rahim Vakili, Maryam Sedghi, Samaneh Noroozi Asl, Sousan Hosseini, Mahsa M Amoli, Hanieh Yaghootkar

    Diterbitkan 2024-10-01
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