Search Results - Rohani, Davood

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  1. 1
    Goiter frequency is more strongly associated with gastric adenocarcinoma than urine iodine level

    Goiter frequency is more strongly associated with gastric adenocarcinoma than urine iodine level by Tabaeizadeh, Mohammad, Haghpanah, Vahid, Keshtkar, Abbasali, Semnani, Shahryar, Roshandel, Gholamreza, Adabi, Khadijeh, Heshmat, Ramin, Rohani, Davood, Kia, Alireza, Hatami, Ehsan, Jahangirrad, Ataollah, Nabizadeh, Ramin, Larijani, Bagher

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  2. 2
    Goiter Frequency Is More Strongly Associated with Gastric Adenocarcinoma than Urine Iodine Level

    Goiter Frequency Is More Strongly Associated with Gastric Adenocarcinoma than Urine Iodine Level by Tabaeizadeh, Mohammad, Haghpanah, Vahid, Keshtkar, Abbasali, Semnani, Shahryar, Roshandel, Gholamreza, Adabi, Khadijeh, Heshmat, Ramin, Rohani, Davood, Kia, Alireza, Hatami, Ehsan, Jahangirrad, Ataollah, Nabizadeh, Ramin, Larijani, Bagher

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  3. 3
    A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population

    A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population by Sadr, Zahra, Zare-Abdollahi, Davood, Rohani, Mohammad, Alavi, Afagh

    Published in Neurological sciences
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  4. 4
    Clinical spectrum in multiple families with primary COQ10 deficiency

    Clinical spectrum in multiple families with primary COQ10 deficiency by Hashemi, Seyyed S., Zare‐Abdollahi, Davood, Bakhshandeh, Mohammad K., Vafaee, Amirreza, Abolhasani, Sona, Inanloo Rahatloo, Kolsoum, DanaeeFard, Fardad, Farboodi, Niloofar, Rohani, Mohammad, Alavi, Afagh

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  5. 5
    Clinical spectrum in multiple families with primary COQ 10 deficiency

    Clinical spectrum in multiple families with primary COQ 10 deficiency by Hashemi, Seyyed S, Zare-Abdollahi, Davood, Bakhshandeh, Mohammad K, Vafaee, Amirreza, Abolhasani, Sona, Inanloo Rahatloo, Kolsoum, DanaeeFard, Fardad, Farboodi, Niloofar, Rohani, Mohammad, Alavi, Afagh

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  6. 6
    Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra

    Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra by Ashrafi, Mahmoud Reza, Mohammadi, Pouria, Tavasoli, Ali Reza, Heidari, Morteza, Hosseinpour, Sareh, Rasulinejad, Maryam, Rohani, Mohammad, Akbari, Masoud Ghahvechi, Malamiri, Reza Azizi, Badv, Reza Shervin, Fathi, Davood, Dehnavi, Ali Zare, Savad, Shahram, Rabbani, Ali, Synofzik, Matthis, Mahdieh, Nejat, Rezaei, Zahra

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  7. 7
    Evaluation of 99mTc-TRODAT-1 SPECT in the diagnosis of Parkinson’s disease versus other progressive movement disorders

    Evaluation of 99mTc-TRODAT-1 SPECT in the diagnosis of Parkinson’s disease versus other progressive movement disorders by Fallahi, Babak, Esmaeili, Atefe, Beiki, Davood, Oveisgharan, Shahram, Noorollahi-Moghaddam, Hamid, Erfani, Mostafa, Tafakhori, Abbas, Rohani, Mohammad, Fard-Esfahani, Armaghan, Emami-Ardekani, Alireza, Geramifar, Parham, Eftekhari, Mohammad

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  8. 8
    Parallel Genome-wide Profiling of Coding and Non-coding RNAs to Identify Novel Regulatory Elements in Embryonic and Maturated Heart

    Parallel Genome-wide Profiling of Coding and Non-coding RNAs to Identify Novel Regulatory Elements in Embryonic and Maturated Heart by Sabour, Davood, Machado, Rui S.R., Pinto, José P., Rohani, Susan, Sahito, Raja G.A., Hescheler, Jürgen, Futschik, Matthias E., Sachinidis, Agapios

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  9. 9
    STRIP2 Is Indispensable for the Onset of Embryonic Stem Cell Differentiation

    STRIP2 Is Indispensable for the Onset of Embryonic Stem Cell Differentiation by Sabour, Davood, Srinivasan, Sureshkumar Perumal, Rohani, Susan, Wagh, Vilas, Gaspar, John Antonydas, Panek, Darius, Ardestani, Mostafa Abootorabi, Doss, Michael Xavier, Riet, Nicole, Abken, Hinrich, Hescheler, Jürgen, Papadopoulos, Symeon, Sachinidis, Agapios

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  10. 10
    Evaluation of (99m)Tc-TRODAT-1 SPECT in the diagnosis of Parkinson's disease versus other progressive movement disorders

    Evaluation of (99m)Tc-TRODAT-1 SPECT in the diagnosis of Parkinson's disease versus other progressive movement disorders by Fallahi, Babak, Esmaeili, Atefe, Beiki, Davood, Oveisgharan, Shahram, Noorollahi-Moghaddam, Hamid, Erfani, Mostafa, Tafakhori, Abbas, Rohani, Mohammad, Fard-Esfahani, Armaghan, Emami-Ardekani, Alireza, Geramifar, Parham, Eftekhari, Mohammad

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  11. 11
    Evaluation of ^sup 99m^Tc-TRODAT-1 SPECT in the diagnosis of Parkinson's disease versus other progressive movement disorders

    Evaluation of ^sup 99m^Tc-TRODAT-1 SPECT in the diagnosis of Parkinson's disease versus other progressive movement disorders by Fallahi, Babak, Esmaeili, Atefe, Beiki, Davood, Oveisgharan, Shahram, Noorollahi-moghaddam, Hamid, Erfani, Mostafa, Tafakhori, Abbas, Rohani, Mohammad, Fard-esfahani, Armaghan, Emami-ardekani, Alireza, Geramifar, Parham, Eftekhari, Mohammad

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  12. 12
    Evaluation of super(99m)Tc-TRODAT-1 SPECT in the diagnosis of Parkinson's disease versus other progressive movement disorders

    Evaluation of super(99m)Tc-TRODAT-1 SPECT in the diagnosis of Parkinson's disease versus other progressive movement disorders by Fallahi, Babak, Esmaeili, Atefe, Beiki, Davood, Oveisgharan, Shahram, Noorollahi-Moghaddam, Hamid, Erfani, Mostafa, Tafakhori, Abbas, Rohani, Mohammad, Fard-Esfahani, Armaghan, Emami-Ardekani, Alireza, Geramifar, Parham, Eftekhari, Mohammad

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