Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Zahra Pirzadeh"'
Autor:
Sajad Pouryousef, Sedigheh Yeganeh, Rouhollah Rouhandeh, Zahra Pirzadeh, Sanaz keshavarzi, Tayebeh bahmani
Publikováno v:
Journal of Advanced Biomedical Sciences, Vol 10, Iss 2, Pp 2186-2196 (2020)
Background & Objective: The early identification of risk factors by screenings methods, as low-cost diagnostic tests with high survival rates, has always been of paramount importance for cancer diagnostics, especially in breast cancer. Since knowledg
Externí odkaz:
https://doaj.org/article/4ab0a5ecad3f4435805e52fb41062d51
Autor:
Mohammad Ghofrani, Hassan Tonekaboni, Parvaneh Karimzadeh, Jafar Nasiri, Zahra Pirzadeh, Mohamadreza Ghazzavi, Omid Yghini
Publikováno v:
International Journal of Preventive Medicine, Vol 9, Iss 1, Pp 69-69 (2018)
Background: Considering that better understanding of the underlying mechanisms and risk factors of arterial ischemic stroke (AIS) would be helpful for better management of stroke and its outcome in children as well as preventing or reducing the occur
Externí odkaz:
https://doaj.org/article/3d6c5894e5634596b4aeda444914c981
Publikováno v:
Journal of Comprehensive Pediatrics. 13
Background: Depending on the level of care and the availability of pediatric intensive care unit (PICU) facilities, the mortality rate of acutely ill children varies in PICUs. Referral of patients from other medical centers, admission during working
Publikováno v:
Chemical Engineering Science. 265:118213
Autor:
Banafsheh Arad, Zahra Pirzadeh
Publikováno v:
International Journal of Pediatrics, Vol 6, Iss 2, Pp 7151-7155 (2018)
Schimke immune-osseous dysplasia (SIOD) is a rare autosomal recessive disorder presented with specific facial features, skeletal dysplasia, steroid resistance nephrotic syndrome (SRNS) and cellular immune insufficiency. This is a SIOD case reported f
Autor:
Seyed-Hasan Tonekaboni, Hamid Nemati, Mohammad-Reza Sharbatdaralaei, Farzad Ahmadabadi, Mohammad Ghofrani, Mohammad-Mahdi Taghdiri, Narjes Jafari, Zahra Pirzadeh, Parvaneh Karimzadeh, Sayena Jabbehdari
Publikováno v:
International Journal of Developmental Disabilities. 61:177-181
Background:Glutaric aciduria type 1 is a rare congenital neurometabolic disorder with autosomal recessive inheritance. This disorder is caused by a defect in glutaryl-CoA dehydrogenase enzyme and presents with hypotonia, spasticity, rigidity, seizure
Autor:
Parvaneh Karimzadeh, Mohamadreza Ghazzavi, Hassan Tonekaboni, Jafar Nasiri, Mohammad Ghofrani, Omid Yghini, Zahra Pirzadeh
Publikováno v:
International Journal of Preventive Medicine, Vol 9, Iss 1, Pp 69-69 (2018)
International Journal of Preventive Medicine
International Journal of Preventive Medicine
Background : Considering that better understanding of the underlying mechanisms and risk factors of arterial ischemic stroke (AIS) would be helpful for better management of stroke and its outcome in children as well as preventing or reducing the occu
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::100e5189bedd10761676ab353d0568d3
http://www.scopus.com/inward/record.url?eid=2-s2.0-84861212249&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84861212249&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
Iranian Journal of Child Neurology
Iranian Journal of Child Neurology
Objective Intractable epilepsy is a serious neurologic problem with different etiologies. Decreased levels of pyridoxal phosphate in cerebral spinal fluid of patients with intractable epilepsy due to pyridoxine dependency epilepsy are reported. The a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0c25703009fa31c74c5812961878fc63
http://www.scopus.com/inward/record.url?eid=2-s2.0-85015797833&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-85015797833&partnerID=MN8TOARS