Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Elham, Pourbakhtyaran"'
Autor:
Nejat Mahdieh, Morteza Heidari, Zahra Rezaei, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinejad, Ali Zare Dehnavi, Masoud Ghahvechi Akbari, Reza Shervin Badv, Elahe Vafaei, Ali Mohebbi, Pouria Mohammadi, Seyyed Mohammad Mahdi Hosseiny, Reza Azizimalamiri, Ali Nikkhah, Elham Pourbakhtyaran, Mohammad Rohani, Narges Khanbanha, Sedigheh Nikbakht, Mojtaba Movahedinia, Parviz Karimi, Homa Ghabeli, Seyed Ahmad Hosseini, Fatemeh Sadat Rashidi, Masoud Garshasbi, Morteza Rezvani Kashani, Noor M. Ghiasvand, Stephan Zuchner, Matthis Synofzik, Mahmoud Reza Ashrafi
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-18 (2024)
Abstract Background To investigate the genetics of early-onset progressive cerebellar ataxia in Iran, we conducted a study at the Children’s Medical Center (CMC), the primary referral center for pediatric disorders in the country, over a three-year
Externí odkaz:
https://doaj.org/article/73901f9896264335a878fdd5b263980b
Autor:
Gholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Sareh Hosseinpour, Roya Haghighi, Elham Pourbakhtyaran, Nahid Khosroshahi, Morteza Heidari
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Objectives This study aimed to analyze the health-related quality of life (HRQoL) of patients with spinal muscular atrophy (SMA) based on the type of SMA, demographic and clinical features and compare HRQoL of these patients with a matched h
Externí odkaz:
https://doaj.org/article/4590cd086b444024a85813ef44d486f1
Autor:
Elham Pourbakhtyaran, Morteza Heidari, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Gholamreza Zamani, Ali Reza Tavasoli, Zahra Rezaei, Setareh Mamishi, Elmira Haji Esmaeil Memar, Seyyed Mohammad Mahdi Hosseiny, Homa Ghabeli, Roya Haghighi, Mahmoud Reza Ashrafi
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract We reported an association between SARS‐CoV‐2 infection and Guillain–Barre syndrome (GBS). From 37 patients with GBS, previous SARS‐CoV‐2 clinical clues, including fever, cough, and diarrhea, were recorded in 18 patients. Among the
Externí odkaz:
https://doaj.org/article/885d23d3f3394b2eaded5d0665d3dfd8
Autor:
Mahmoud Reza Ashrafi, Elham Pourbakhtyaran, Mohammad Rohani, Bita Shalbafan, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinezhad, Zahra Rezaei, Ali Zare Dehnavi, Seyyed Mohammad Mahdi Hosseiny, Roya Haghighi, Homa Ghabeli, Morteza Heidari
Publikováno v:
Clinical Case Reports, Vol 10, Iss 4, Pp n/a-n/a (2022)
Abstract Autosomal recessive cerebellar ataxias are a group of heterogeneous early‐onset progressive disorders that some of them are treatable. We performed a 4‐year follow‐up for 25 patients who had treatable ataxia. According to our study, pa
Externí odkaz:
https://doaj.org/article/d669e88a76874f04803a1c12ee0f33ce
Autor:
Hojjat Derakhshanfar, Elham Pourbakhtyaran, Samane Rahimi, Samira Sayyah, Fereshteh Karbasian, Zahra Soltantooyeh, Shahrzad Fallah
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 8, Iss 11, Pp 3700-3705 (2019)
Introduction: Abdominal pain, in particular appendicitis, is a common cause of emergency department visits in children. Therefore, early diagnosis is very important. There are different scoring systems for the diagnosis of appendicitis. This study is
Externí odkaz:
https://doaj.org/article/3233458fb5e14c52a39e62169be29439
Autor:
Niloufar Bineshfar, Alireza Mirahmadi, Fereshteh Karbasian, Elham Pourbakhtyaran, Abdollah Karimi, Mehdi Sarafi
Publikováno v:
Case Reports in Pediatrics, Vol 2021 (2021)
Coronavirus disease-2019 (COVID-19) which is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has spread throughout the world causing problems for millions of people. Symptoms of COVID-19 in pediatric patients include both respi
Externí odkaz:
https://doaj.org/article/8613a6cef88e4ed7bea14171edb291ac
Autor:
Seyedeh Atiyeh Afjei, Mohammad Farid Mohammadi, Elham Pourbakhtyaran, Homa Ghabeli, Mahmoud Reza Ashrafi, Roya Haghighi, Maryam Rasulinezhad, Neda Pak, Ali Reza Tavasoli, Morteza Heidari
Publikováno v:
neurogenetics. 24:67-78
Autor:
Mahmoud Reza Ashrafi, Roya Haghighi, Reza Shervin Badv, Homa Ghabeli, Ali Reza Tavasoli, Elham Pourbakhtyaran, Zahra Rezaei, Nejat Mahdieh, Pouria Mohammadi, Morteza Heidari
Publikováno v:
Journal of Molecular Neuroscience. 72:1125-1132
Coenzyme Q10 deficiency can be due to mutations in Coenzyme Q10-biosynthesis genes (primary) or genes unrelated to biosynthesis (secondary). Primary Coenzyme Q10 deficiency-4 (COQ10D4), also known as autosomal recessive spinocerebellar ataxia-9 (SCAR
Autor:
Mehdi Sarafi, Niloufar Bineshfar, Alireza Mirahmadi, Abdollah Karimi, Fereshteh Karbasian, Elham Pourbakhtyaran
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2021 (2021)
Case Reports in Pediatrics, Vol 2021 (2021)
Coronavirus disease-2019 (COVID-19) which is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has spread throughout the world causing problems for millions of people. Symptoms of COVID-19 in pediatric patients include both respi
Autor:
Yashar Yousefzadeh-fard, Mohammad Hadi Gharedaghi, Sara Esmaeili, Elham Pourbakhtyaran, Mohammad Salehi Sadaghiani
Publikováno v:
Basic and Clinical Neuroscience, Vol 4, Iss 4, Pp 307-314 (2013)
Introduction: Addiction imposes a large medical, social and economic burden on societies. Currently, there is no effective treatment for addiction. Our struggle to decipher the different mechanisms involved in addiction requires a proper understandin
Externí odkaz:
https://doaj.org/article/e121675a833a4cc085e8f704e21558ba