Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Nader Shakibazad"'
Autor:
Kosar Rahimi, Hamid Amoozgar, Soheila Zareifar, Mahdi Shahriari, Omid Reza Zekavat, Mehran Karimi, Gholamreza Fathpour, Fazl Saleh, Nader Shakibazad, Shayan Bordbar, Mohammadreza Bordbar
Publikováno v:
The Egyptian Heart Journal, Vol 75, Iss 1, Pp 1-8 (2023)
Abstract Background Cardiotoxicity is a major concern following doxorubicin (DOX) use in the treatment of malignancies. We aimed to investigate whether deferoxamine (DFO) can prevent acute cardiotoxicity in children with cancer who were treated with
Externí odkaz:
https://doaj.org/article/e1508f40c5df4d599281c38bebf0f17c
Autor:
Naser Honar, Najmeh Nezamabadipour, Seyed Mohsen Dehghani, Mahmood Haghighat, Mohammad Hadi Imanieh, Maryam Ataollahi, Nader Shakibazad, Hazhir Javaherizadeh
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background The most common infection in children with the hepatic disease with or without cirrhotic ascites is spontaneous bacterial peritonitis (SBP), which occurs in the absence of an evident intra-abdominal source of infection. The presen
Externí odkaz:
https://doaj.org/article/55386e9c36f445a2a97035c8adc952ab
Autor:
Mohammadreza Bordbar, Nader Shakibazad, Hadi Mottaghipisheh, Mahdi Shahriari, Soheila Zareifar, Omid Reza Zekavat
Publikováno v:
Middle East Journal of Cancer, Vol 11, Iss 4, Pp 512-515 (2020)
Acute lymphoblastic leukemia has several presentations associated with bone marrow and extramedullary involvement. The unusual presentation may be due to the infiltration of leukemic cells in any organ. An 11-year-old girl presented with fever and vo
Externí odkaz:
https://doaj.org/article/70db8ad332b941ad8d22ce932b3a3805
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report
Autor:
Soheila Zareifar, Hassan Dastsooz, Mahdi Shahriari, Mohammad Ali Faghihi, Golsa Shekarkhar, Mohammadreza Bordbar, Omid Reza Zekavat, Nader Shakibazad
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Fanconi anemia (FA) is a heterogeneous genetic disorder characterized by congenital anomalies, early-onset bone marrow failure, and a high predisposition to cancers. Up to know, different genes involved in the DNA repair pathway,
Externí odkaz:
https://doaj.org/article/f2f41e11bd784c0582bb06bdaf339fe1
Publikováno v:
Middle East Journal of Cancer, Vol 9, Iss 3, Pp 202-207 (2018)
Background: Folate and vitamin B12 have a number of biologic roles that make them important in hematological disorders and malignancy. In the present study, we have assessed serum folate and vitamin B12 levels and their associated variables in patien
Externí odkaz:
https://doaj.org/article/ffb31021f1c84521bfebfb11c746116e
Autor:
Omid Reza Zekavat, Alireza Sahraian, Somayeh Esmaili, Sezaneh Haghpanah, Susan Rabie, Farzaneh Alipour, Reza Bahrami, Nader Shakibazad
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 5, Pp SC01-SC03 (2019)
Introduction: Zinc and copper have a main role as nutrients in the growth and development of neonates. Aim: To evaluate the relationship of birth weight, feeding, and Gestational Age (GA) with serum copper and zinc in preterm neonates. Materials and
Externí odkaz:
https://doaj.org/article/06f9f43712d14141a0b7a848384290e4
Publikováno v:
Middle East Journal of Cancer, Vol 8, Iss 3, Pp 167-169 (2017)
Externí odkaz:
https://doaj.org/article/918fe41036ee4cbf8889897d1fef7fdc
Autor:
Omid Reza Zekavat, Gholamreza Fathpour, Mohammadreza Bordbar, Sezaneh Haghpanah, Nader Shakibazad
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 2, Pp SD01-SD03 (2018)
Drug induced thrombocytopenia is uncommon cause of life-threatening bleeding. The mechanisms may include bone marrow suppression or antibody-mediated platelet destruction. We report the case of a two-year-old boy with incedental ingestion of Buparvaq
Externí odkaz:
https://doaj.org/article/07a9e38770c24ea5a7453e1725a5eaa9
Autor:
Ali Amanati, Nader Shakibazad, Bahman Pourabbas, Mohammad Hossein Nowroozzadeh, Soheila Zareifar, Omid Reza Zekavat
Publikováno v:
Case Reports in Medicine, Vol 2018 (2018)
Cytomegalovirus (CMV) retinitis is one of the rare but debilitating presentations of the CMV infection in children with leukemia. Herein, we report a 12-year-old boy with acute myeloid leukemia complicated by rapid progressive visual loss during rela
Externí odkaz:
https://doaj.org/article/6e7df8b4b59341179fbb95d05669a1d3
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 8, Pp XD01-XD02 (2017)
Esthesioneuroblastoma is a rare malignant tumour of the olfactory epithelium. The most common symptom is related to unilateral nasal obstruction. It rarely presents with bilateral proptosis and blindness. We report a 21-month-old girl with esthesion
Externí odkaz:
https://doaj.org/article/d152639ba1ae4a05ab9cf70addb6ae6b