檢索結果 - Tavasoli, Ali Reza

Neurological and Vascular Manifestations of Ethylmalonic Encephalopathy 由 TAVASOLI, Ali Reza, ROSTAMI, Parastoo, ASHRAFI, Mahmoud Reza, KARIMZADEH, Parvaneh

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Farber disease: report of three cases with joint involvement mimicking juvenile idiopathic arthritis 由 Moghadam, Soheila Hoseinzadeh, Tavasoli, Ali Reza, Modaresi, Mohammadreza, Ziaee, Vahid

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Dosimetry of gamma chamber blood irradiator using PAGAT gel dosimeter and Monte Carlo simulations 由 Mohammadyari, Parvin, Zehtabian, Mehdi, Sina, Sedigheh, Tavasoli, Ali Reza, Faghihi, Reza

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Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases 由 ASHRAFI, Mahmoud Reza, TAVASOLI, Ali Reza, ALIZADEH, Houman, ZARE NOGHABI, Javad, PARVANEH, Nima

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Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations 由 Tavasoli, Ali Reza, Parvaneh, Nima, Ashrafi, Mahmoud Reza, Rezaei, Zahra, Zschocke, Johannes, Rostami, Parastoo

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A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family 由 Sepahvand, Afrooz, Razmara, Ehsan, Bitarafan, Fatemeh, Galehdari, Mohammad, Tavasoli, Ali Reza, Almadani, Navid, Garshasbi, Masoud

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Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1: a case report 由 Khalesi, Raziyeh, Razmara, Ehsan, Asgaritarghi, Golareh, Tavasoli, Ali Reza, Riazalhosseini, Yasser, Auld, Daniel, Garshasbi, Masoud

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Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants 由 Mahdieh, Nejat, Soveizi, Mahdieh, Tavasoli, Ali Reza, Rabbani, Ali, Ashrafi, Mahmoud Reza, Kohlschütter, Alfried, Rabbani, Bahareh

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Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report 由 Zardadi, Safoura, Razmara, Ehsan, Rasoulinezhad, Maryam, Babaei, Meisam, Ashrafi, Mohammad Reza, Pak, Neda, Garshasbi, Masoud, Tavasoli, Ali Reza

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Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation 由 Vafaee‐Shahi, Mohammad, Ghasemi, Saeide, Beiraghi Toosi, Mehran, Ashrafi, Mahmoud Reza, Badv, Reza Shervin, Tavasoli, Ali Reza, Tahernia, Leila

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RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant 由 Kameli, Reyhaneh, Amanat, Man, Rezaei, Zahra, Hosseionpour, Sareh, Nikbakht, Sedigheh, Alizadeh, Houman, Ashrafi, Mahmoud Reza, Omrani, Abdolmajid, Garshasbi, Masoud, Tavasoli, Ali Reza

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Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case report 由 Aryan, Hajar, Razmara, Ehsan, Farhud, Dariush, Zarif-Yeganeh, Marjan, Zokaei, Shaghayegh, Hassani, Seyed Abbas, Ashrafi, Mahmoud Reza, Garshasbi, Masoud, Tavasoli, Ali Reza

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Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy 由 Ashrafi, Mahmoud Reza, Haghighi, Roya, Badv, Reza Shervin, Ghabeli, Homa, Tavasoli, Ali Reza, Pourbakhtyaran, Elham, Rezaei, Zahra, Mahdieh, Nejat, Mohammadi, Pouria, Heidari, Morteza

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Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy 由 Zamani, Gholamreza, Hosseinpour, Sareh, Ashrafi, Mahmoud Reza, Mohammadi, Mahmoud, Badv, Reza Shervin, Tavasoli, Ali Reza, Akbari, Masood Ghahvechi, Bereshneh, Ali Hosseini, Malamiri, Reza Azizi, Heidari, Morteza

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ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants 由 Dehnavi, Ali Zare, Heidari, Erfan, Rasulinezhad, Maryam, Heidari, Morteza, Ashrafi, Mahmoud Reza, Hosseini, Mohammad Mahdi, Sadeghzadeh, Fatemeh, Fallah, Mohammad-Sadegh, Rostampour, Noushin, Bahraini, Amir, Garshasbi, Masoud, Tavasoli, Ali Reza

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Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study 由 Ashrafi, Mahmoud Reza, Pourbakhtyaran, Elham, Rohani, Mohammad, Shalbafan, Bita, Tavasoli, Ali Reza, Hosseinpour, Sareh, Rasulinezhad, Maryam, Rezaei, Zahra, Zare Dehnavi, Ali, Hosseiny, Seyyed Mohammad Mahdi, Haghighi, Roya, Ghabeli, Homa, Heidari, Morteza

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Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical tria... 由 Amanat, Man, Majmaa, Anahita, Zarrabi, Morteza, Nouri, Masoumeh, Akbari, Masood Ghahvechi, Moaiedi, Ali Reza, Ghaemi, Omid, Zamani, Fatemeh, Najafi, Sharif, Badv, Reza Shervin, Vosough, Massoud, Hamidieh, Amir Ali, Salehi, Mona, Montazerlotfelahi, Hadi, Tavasoli, Ali Reza, Heidari, Morteza, Mohebi, Hossein, Fatemi, Ali, Garakani, Amir, Ashrafi, Mahmoud Reza

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The safety and efficacy of umbilical cord blood mononuclear cells in individuals with spastic cerebral palsy: a randomized double-blind sham-controlled clinical trial 由 Zarrabi, Morteza, Akbari, Masood Ghahvechi, Amanat, Man, Majmaa, Anahita, Moaiedi, Ali Reza, Montazerlotfelahi, Hadi, Nouri, Masoumeh, Hamidieh, Amir Ali, Badv, Reza Shervin, Karimi, Hossein, Rabbani, Ali, Mohebbi, Ali, Rahimi-Dehgolan, Shahram, Rahimi, Rosa, Dehghan, Ensieh, Vosough, Massoud, Abroun, Saeed, Shamsabadi, Farhad Mahvelati, Tavasoli, Ali Reza, Alizadeh, Houman, Pak, Neda, Zamani, Gholam Reza, Mohammadi, Mahmoud, Javadzadeh, Mohsen, Ghofrani, Mohammad, Hassanpour, Seyed Hossein, Heidari, Morteza, Taghdiri, Mohammad Mehdi, Mohseni, Mohamad Javad, Noparast, Zahra, Masoomi, Safdar, Goudarzi, Mehrdad, Mohamadpour, Masood, Shodjaee, Razieh, Samimi, Solaleh, Mohammad, Monireh, Gholami, Mona, Vafaei, Nahid, Koochakzadeh, Leyli, Valizadeh, Amir, Malamiri, Reza Azizi, Ashrafi, Mahmoud Reza

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