Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Wesam A, Mokhtar"'
Autor:
Laila Sherief, Elhamy R. Abd El-khalek, Ibrahim A. Libda, Osama A. Gaber, Naglaa M. Kamal, Basma K. Soliman, Wesam A. Mokhtar, Gehad M. Kamar, Marwa Zakaria
Publikováno v:
Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp S2- (2023)
Externí odkaz:
https://doaj.org/article/a0727f9b90c246119c1e1a74f4b3be71
Autor:
Nahla Ibrahim Zidan, Doaa Metwally AbdElmonem, Haitham Mohamed Elsheikh, Elsayed Anany Metwally, Wesam AbdElmonem Mokhtar, Gamal Mohamed Osman
Publikováno v:
Platelets, Vol 32, Iss 5, Pp 642-650 (2021)
Inherited thrombocytopenias are a heterogeneous group of diseases characterized by a reduced number of platelets and a bleeding tendency that ranges from very mild to life threatening especially in surgery. Mutations in the 5′ untranslated region (
Externí odkaz:
https://doaj.org/article/a8dc618b61d246678946df20b53013bb
Publikováno v:
Iranian Journal of Neonatology, Vol 12, Iss 2, Pp 1-7 (2021)
Background: Although a great improvement has been achieved in the outcome of sick neonates with the effectivewidespread introduction of mechanical ventilation in neonatal intensive care units, a significant proportion of highfatality is still detecte
Externí odkaz:
https://doaj.org/article/ad17db2b6687482f88b6d6d61d4962bc
Autor:
Laila M. Sherief, Osama A. Gaber, Hala Mosaad Youssef, Hanan S. Sherbiny, Wesam a Mokhtar, Asmaa A. A. Ali, Naglaa M. Kamal, Yehia H. Abdel Maksoud
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-7 (2020)
Abstract Background Hemophilia A (HA) is an X-linked recessive bleeding disorder characterized by qualitative and quantitative deficiency of factor VIII (FVIII). The development of inhibitor antibodies against FVIII is the most challenging complicati
Externí odkaz:
https://doaj.org/article/8eaf0b22d735476d8a8f450d26b6a366
Autor:
Laila M. Sherief, Mohamed Beshir, Nermin Raafat, Elhamy R. Abdelkhalek, Wesam A. Mokhtar, Khaled M. Elgerby, Basma K. Soliman, Hosam E. Salah, Ghada A. Mokhtar, Naglaa M. Kamal, Heba ELsayed, Marwa Zakaria
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Background Osteonecrosis (ON) is one of the major therapy‐related complications in childhood acute lymphoblastic leukemia (ALL). The purpose of the current study is to assess the frequency of ON in children with ALL and to detect whether p
Externí odkaz:
https://doaj.org/article/50185a15b44e4cadad9f68749736c8e1
Publikováno v:
Genes and Diseases, Vol 6, Iss 2, Pp 193-200 (2019)
Vitamin D & vitamin D receptor (VDR) signaling play a very crucial role in early embryonic heart development. We construct this case-control study to investigate the association between maternal serum vitamin D level & VDR gene Fok1 polymorphism and
Externí odkaz:
https://doaj.org/article/d6e5a3546b274ab788311606b31d3766
Autor:
Laila M. Sherief, Elhamy R. Abd El-khalek, Ibrahim A. Libda, Osama A. Gaber, Naglaa M. Kamal, Basma K. Soliman, Wesam A. Mokhtar, Ghada A. Mokhtar, Hosam E. Salah, Gehad M. Kamar, Marwa Zakaria
Publikováno v:
Therapeutic Advances in Chronic Disease, Vol 12 (2021)
Background: An increased risk of cardiovascular complications is reported in survivors of childhood acute lymphoblastic leukemia (ALL). Early identification of impaired vascular health may allow for early interventions to improve outcomes. Aim: The s
Externí odkaz:
https://doaj.org/article/b423f1d3829545d1976e04e9896dba96
Autor:
Amira Mobarak, Heba Dawoud, Wesam A. Mokhtar, Abdelrahim A. Sadek, Gihan Mohamed Bebars, Amr Ahmed Othman, Rofaida M. Magdy, Hanaa Nofal, Amr Zoair
Publikováno v:
International Journal of Pediatrics, Vol 2020 (2020)
PA and MAA have numerous nonspecific presentations, potentially leading to delayed diagnosis or misdiagnosis. In this paper, we present the clinical and biochemical characteristics of MMA and PA patients at initial presentation. Results. This is a re
Externí odkaz:
https://doaj.org/article/69b88236a1fa4f88bfb9144fe8e927d6
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 66, Iss 4, Pp 115-120 (2018)
Background: Caffeine citrate is the methyl-xanthine of choice used in controlling apnea of prematurity (AOP). Caffeine central effect is mediated via non-selective (A1) and selective (A2a) adenosine receptors antagonism. Variability in caffeine respo
Externí odkaz:
https://doaj.org/article/fcfae87fcfe64efea1d49536abe9ffef
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 48, Iss 4, Pp 971-975 (2017)
Aim: The aim of this study is to evaluate the role of high resolution ultrasonography (HRUS) of the hip in premature neonates admitted to the neonatal intensive care unit (NICU) in diagnosis of septic hip arthritis. Patients and methods: This prospec
Externí odkaz:
https://doaj.org/article/152956f8eec24cb2a8cddc7f6942c401