Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Behdad Gharib"'
Autor:
Elaheh Malakan Rad, Nazli Parizadeh, Hassan Radmehr, Toktam Sheykhian, Behdad Gharib, Aliakbar Zeinaloo
Publikováno v:
The Egyptian Heart Journal, Vol 76, Iss 1, Pp 1-12 (2024)
Abstract Background Right atrial pressure plays a critical role as a hemodynamic parameter in diagnosing pulmonary hypertension and other cardiac diseases, as well as guiding the treatment and prognosis of various cardiac disorders. If there is no ob
Externí odkaz:
https://doaj.org/article/aa9a474c265a42959c6d9051b0354cfa
Publikováno v:
Case Reports in Clinical Practice, Vol 8, Iss 5 (2024)
Pompe disease or type 2 glycogen storage disease (GSD), is an autosomal recessive disorder, occurs by deficiency of an enzyme (acid maltase) which degrades glycogen in lysosomes. It is classified into infantile and late onset types.Identifying PD pre
Externí odkaz:
https://doaj.org/article/f94baf9461f74b81bdd5eb95f0886f50
Publikováno v:
Health Science Reports, Vol 7, Iss 1, Pp n/a-n/a (2024)
Abstract Background and Aims Acute kidney injury (AKI) is a common complication in pediatric cardiac intensive care unit (CICU). This study aims to identify the prevalence, risk factors, and outcomes of AKI in pediatrics admitted to a CICU unit of a
Externí odkaz:
https://doaj.org/article/d432c154178a4136bcc8445b6058f8b8
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:
Tina Eshaghian, Bahareh Rabbani, Reza Shervin Badv, Sahar Mikaeeli, Behdad Gharib, Stanley Iyadurai
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100553- (2023)
Externí odkaz:
https://doaj.org/article/58798953cb874275a9103a0b9a58b38a
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:
Ziba Mosayebi, Mohammadreza Mirzaaghayan, Reza Shabanian, Behdad Gharib, Elahe Movahedi, minoo dadkhah, Reihaneh Mohsenipour, Maryam Saeedi
Publikováno v:
Iranian Journal of Neonatology, Vol 11, Iss 2, Pp 112-116 (2020)
Background: Neonatal thrombotic diseases can cause mortality or serious morbidity and disability.Case report: In this report, we present a case of neonatal inferior vena cava thromboembolism with several underlyingfactors. Hereditary thrombophilia an
Externí odkaz:
https://doaj.org/article/c24b4ca1e89140bdbbfccd07b08842e2
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