Ali Reza Tavasoli, MD

Получаване на мой собствен потребителски профил

Позовавания

	Всички	От 2019
Позовавания	840	727
h-индекс	16	15
i10-индекс	26	21

180

135

201420152016201720182019202020212022202320248 11 18 32 33 52 89 147 167 179 91

Публичен достъп

Преглед на всички

14 статии

3 статии

налични

неналични

Въз основа на изисквания при финансирането

Съавтори

Masoud GarshasbiAssociate Professor of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares UniversityПотвърден имейл адрес: modares.ac.ir
Reza Shervin BadvPediatric Neurologist and Epileptologist; Associate Professor, Children's Medical Center, PediatricsПотвърден имейл адрес: sina.tums.ac.ir
Nejat MahdiehRajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, IranПотвърден имейл адрес: rhc.ac.ir
parastoo rostamiassociate professorПотвърден имейл адрес: sina.tums.ac.ir
Bahareh RabbaniIran University of Medical SciencesПотвърден имейл адрес: modares.ac.ir
mohammad rohaniProfessor of neurology, Iran University of Medical SciencesПотвърден имейл адрес: iums.ac.ir
Mohammad Vafaee ShahiAssociate Professor of Pediatric Neurology, Iran University of Medical SciencesПотвърден имейл адрес: iums.ac.ir
Ali Hosseini Bereshneh,Baylor College of Medicine; Texas Children's Hospital; Jan and Dan Duncan Neurological ResearchПотвърден имейл адрес: bcm.edu
Reza AzizimalamiriAssistant Professor of Pediatric NeurologyПотвърден имейл адрес: ajums.ac.ir
Nima ParvanehAssociate Professor of Pediatrics, Tehran University of Medical SciencesПотвърден имейл адрес: tums.ac.ir
Sedighe NikbakhtLorestan University of Medical SciencesПотвърден имейл адрес: lums.ac.ir
Johannes ZschockeПотвърден имейл адрес: i-med.ac.at
Massoud HoushmandProfessor in Genetic Diagnostic department; NIGEBПотвърден имейл адрес: nigeb.ac.ir
P KarimzadehShahid Beheshti University of Medical SciencesПотвърден имейл адрес: sbmu.ac.ir
Maryam MahmoudiTehran University of Medical SciencesПотвърден имейл адрес: sina.tums.ac.ir
parviz karimiilam university of medical sciencesПотвърден имейл адрес: medilam.ac.ir
Maryam MasoudiTehran University of Medical SciencesПотвърден имейл адрес: student.tums.ac.ir
soodeh salehiGuilan university of medical sciencesПотвърден имейл адрес: gums.ac.ir
Nima RezaeiTehran University of Medical Sciences; Universal Scientific Education and Research Network (USERN)Потвърден имейл адрес: tums.ac.ir
Nafissi, ShahriarProfessor of Neurology, Neuromuscular Research Center, Tehran University of medical sciencesПотвърден имейл адрес: sina.tums.ac.ir

Следене

Ali Reza Tavasoli, MD

Associate professor of pediatric neurology, TUMS, Phoenix Children's Hospital

Потвърден имейл адрес: sina.tums.ac.ir

Leukodystrophies Neurogenetic Disorders Headache Neuroinflammatory Disorders


Заглавие Сортиране по цитати Сортиране по година Сортиране по заглавие	Позовавания Позовавания	Година
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies MR Ashrafi, M Amanat, M Garshasbi, R Kameli, Y Nilipour, M Heidari, ... Expert review of neurotherapeutics 20 (1), 65-84, 2020	69	2020
The effects of classic ketogenic diet on serum lipid profile in children with refractory seizures GR Zamani, M Mohammadi, MR Ashrafi, P Karimi, M Mahmoudi, RS Badv, ... Acta Neurologica Belgica 116, 529-534, 2016	69	2016
Childhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management MR Ashrafi, AR Tavasoli Brain and Development 39 (5), 369-385, 2017	44	2017
Efficacy and safety of cinnarizine in the prophylaxis of migraine in children: a double-blind placebo-controlled randomized trial MR Ashrafi, S Salehi, RA Malamiri, M Heidari, SA Hosseini, M Samiei, ... Pediatric Neurology 51 (4), 503-508, 2014	44	2014
Effects of miglustat on stabilization of neurological disorder in Niemann–Pick disease type C: Iranian pediatric case series P Karimzadeh, SH Tonekaboni, MR Ashrafi, Y Shafeghati, A Rezayi, ... Journal of Child Neurology 28 (12), 1599-1606, 2013	31	2013
Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical … M Amanat, A Majmaa, M Zarrabi, M Nouri, MG Akbari, AR Moaiedi, ... Stem Cell Research & Therapy 12, 1-15, 2021	23	2021
Coronavirus, its neurologic manifestations, and complications MR Ashrafi, R Azizimalamiri, RS Badv, AR Tavasoli, A Nikkhah, ... Iranian Journal of Pediatrics 30 (2), 2020	22	2020
Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants N Mahdieh, M Soveizi, AR Tavasoli, A Rabbani, MR Ashrafi, ... Scientific reports 11 (1), 3231, 2021	21	2021
Cinnarizine and sodium valproate as the preventive agents of pediatric migraine: A randomized double-blind placebo-controlled trial M Amanat, M Togha, E Agah, M Ramezani, AR Tavasoli, R Azizi Malamiri, ... Cephalalgia 40 (7), 665-674, 2020	20	2020
Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations AR Tavasoli, N Parvaneh, MR Ashrafi, Z Rezaei, J Zschocke, P Rostami Orphanet Journal of Rare Diseases 13, 1-8, 2018	20	2018
Identification of novel loss of function variants in MBOAT7 resulting in intellectual disability E Heidari, A Caddeo, K Zarabadi, M Masoudi, AR Tavasoli, S Romeo, ... Genomics 112 (6), 4072-4077, 2020	19	2020
Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case report H Aryan, E Razmara, D Farhud, M Zarif-Yeganeh, S Zokaei, SA Hassani, ... BMC neurology 20, 1-11, 2020	18	2020
The first report of relative incidence of inherited white matter disorders in an Asian country based on an Iranian bioregistry system MR Ashrafi, Z Rezaei, M Heidari, S Nikbakht, RA Malamiri, M Mohammadi, ... Journal of Child Neurology 33 (4), 255-259, 2018	17	2018
Alexander disease: report of two unrelated infantile form cases, identified by GFAP mutation analysis and review of literature; the first report from Iran MR Ashrafi, A Tavasoli, O Aryani, H Alizadeh, M Houshmand Iranian Journal of Pediatrics 23 (4), 481, 2013	17	2013
Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review P Rostami, S Hosseinpour, MR Ashrafi, H Alizadeh, M Garshasbi, ... Acta Neurologica Belgica 120, 511-516, 2020	16	2020
RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant R Kameli, M Amanat, Z Rezaei, S Hosseionpour, S Nikbakht, H Alizadeh, ... Orphanet Journal of Rare Diseases 14, 1-7, 2019	16	2019
Levetiracetam for prophylactic treatment of pediatric migraine: A randomized double-blind placebo-controlled trial H Montazerlotfelahi, M Amanat, AR Tavasoli, E Agah, GR Zamani, ... Cephalalgia 39 (12), 1509-1517, 2019	15	2019
Alexander disease: a leukodystrophy that may mimic brain tumor A Tavasoli, T Armangue, CY Ho, M Whitehead, M Bornhorst, J Rhee, ... Journal of child neurology 32 (2), 184-187, 2017	14	2017
Novel neuroclinical findings of autosomal recessive primary microcephaly 15 in a consanguineous Iranian family E Razmara, H Azimi, AR Tavasoli, E Fallahi, SV Sheida, M Eidi, A Bitaraf, ... European Journal of Medical Genetics 63 (12), 104096, 2020	13	2020
Homozygous in‐frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family E Heidari, E Razmara, S Hosseinpour, AR Tavasoli, M Garshasbi Annals of human genetics 84 (4), 315-323, 2020	11	2020

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