Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Sara Memarian"'
Autor:
Reza Shervin Badv, Fakhreddin Shariatmadari, Shiva Bayat, Sara Memarian, Samaneh Esteghamat Hanzae, Hossein Yousefimanesh
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-4 (2024)
Abstract Background Progressive myoclonic epilepsy is a clinically and genetically heterogeneous group of diseases characterized by myoclonic seizures, drug-resistant epilepsy and neurodevelopmental regression. The disease is attributed to mutations
Externí odkaz:
https://doaj.org/article/650803acae5549468827c4b99f9dd443
Autor:
Elmira Hajiesmaeil Memar, Fatemeh Tahghighi, Sedigheh Yousefzadegan, Parisa Sadeghirad, Ashraf Mousavi, Ramin Zare Mahmoudabadi, Hossein Saeidi, Mehri Ayati, Sahar Naderi, Sara Memarian, Seyedmusa Zeinalabedin, Bahar Ashjaei, Hojatollah Raji, Leila Tahernia, Hosein Alimadadi, Vahid Ziaee
Publikováno v:
Case Reports in Surgery, Vol 2024 (2024)
Background. On December 2019, a novel coronavirus disease (COVID-19) spread worldwide and became a pandemic. Multisystem inflammatory syndrome in children (MIS-C) due to cytokine release syndrome following COVID-19 presents with various manifestation
Externí odkaz:
https://doaj.org/article/55f262ef11bb4c7f9a76f6a23e27c423
Publikováno v:
Health Science Reports, Vol 6, Iss 12, Pp n/a-n/a (2023)
Abstract Background and Aims In the pathophysiology of Guillain–Barre syndrome (GBS), inflammation and immunity are believed to play a key role. The neutrophil‐lymphocyte ratio (NLR), monocyte‐lymphocyte ratio (MLR), and platelet‐lymphocyte r
Externí odkaz:
https://doaj.org/article/730a50da3a234327af435065a2846a48
Autor:
Alireza Abdshah, Mohammadreza Mirzaaghayan, Morteza Heidari, Sara Memarian, Mobina Amanollahi, Azadeh Nazeri, Behdad Gharib
Publikováno v:
Health Science Reports, Vol 6, Iss 1, Pp n/a-n/a (2023)
Abstract Background and Aims Due to increased rate of open‐heart surgeries in children, postsurgical mortality and morbidities have increasingly gained attention. Neurological complications are some of the most important postsurgical events. Howeve
Externí odkaz:
https://doaj.org/article/543b3a28dbd544a394977f14807e14ce
Autor:
Mohammad Taghi Majnoon, Behdad Gharib, Sara Memarian, Azade Rastgar, Mahsa Naemi, Alireza Golbabaei
Publikováno v:
Journal of Pediatrics Review, Vol 9, Iss 3, Pp 255-262 (2021)
Vein of Galen Aneurysmal Malformations (VGAMs) are severe and rare congenital brain vasculature anomalies, which causes high mortality and morbidity in fetuses, neonates, and infants. It can be identified in the pregnancy period with fetal echocardio
Externí odkaz:
https://doaj.org/article/148b944cfbfb4fe9a44eda07828b661c
Autor:
Alireza Golbabaei, Sara Memarian, Mahsa Naemi, Azade Rastgar, Rana Karimi, Behdad Gharib, Mohamad Taghi Majnoon
Publikováno v:
Journal of Pediatrics Review, Vol 9, Iss 2, Pp 153-158 (2021)
Common arterial trunk (persistent truncus arteriosus) is a rare, congenital heart anomaly and characterized by Ventricular Septal Defect (VSD), single truncal valve, and a common ventricular outflow tract. We reported a case of truncus arteriosus typ
Externí odkaz:
https://doaj.org/article/c4bad80b19d241e8afaeb68ff2213d1a
Autor:
Hedayatollah Nahvi, Sara Memarian, Mohammadtaghi Majnoon, Behdad Gharib, Mohammad Es-hagh Rozeh, Mojtaba Gorji, Somayeh Jafrasteh, Zeinab Najafi, Rahman Khosravi
Publikováno v:
Iranian Journal of Pediatric Surgery, Vol 4, Iss 2, Pp 101-104 (2018)
Rectal adenocarcinoma is rare in children. The patient described here is a 9-year-old girl who presented with rectorrhagia. Her problem started 3 months ago and she had been treated for infectious diarrhea. A colonoscopy was performed 3 months after
Externí odkaz:
https://doaj.org/article/ba36976b8fa343608ed1d178cf2eda73
Autor:
Reza Shervin Badv, Sara Memarian, Masoud Ghahvechi, Hossein Farshad Moghaddam, Maryam Saidi, Reihaneh Mohsenipour, Parisa Rahmani, Bahram Yarali, Mojtaba Gorji, Behdad Gharib
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 4, Iss 12, Pp 35-38 (2018)
Congenital Myasthenic Syndromes (CMS) are rare inherited disorders characterized by dysfunction of neuromuscular transmission at the neuromuscular junction. Most patients with congenital myasthenic syndromes present in the infancy. Major symptoms of
Externí odkaz:
https://doaj.org/article/fb28ad3022b04b1db09af02ae2d97dbe
Autor:
Mohammad Tajdini, Mansoureh Shariat, Mohammadreza Mizaaghayan, Sara Memarian, Parisa Rahmani, Mohammadtaghi Majnoon
Publikováno v:
Case Reports in Clinical Practice, Vol 2, Iss 1 (2017)
This report describes two patients (a 7-year-old boy and a 3-month-old boy) who have had chronic and recurrent respiratory distress and wheezing episodes since infancy. The elder one had been treated for hyper-reactive airway disease and asthma, and
Externí odkaz:
https://doaj.org/article/6d46da6679e94f0491c4b640b033f1cf
Autor:
Behdad Gharib, Masoud Mohammadpour, Meisam Sharifzadeh, Fatemeh Mirashrafi, Bahareh Yaghmaie, Neda Pak, Mehrzad Mehdizadeh, Hamid Eshaghi, Mojtaba Gorji, Sara Memarian
Publikováno v:
Acta Medica Iranica, Vol 54, Iss 12 (2017)
Parapharyngeal abscess is a life-threatening disease. Upper respiratory tract infection is the main cause in children. We present a 15-month-old boy admitted to the emergency ward with the chief complaint of difficulty in breathing caused by paraphar
Externí odkaz:
https://doaj.org/article/d3f7ad2e6d704e73b1d109731729c7a6