Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Iman Ehsan Abdel Meguid"'
Autor:
Walaa Fakher, Dina El-Tabie, Nihal Mohamed El-Refaie, Iman Ehsan Abdel-Meguid, Radwa Ezzat Amin, Hala Ahmed El-Gindy
Publikováno v:
Journal of Child Science. 11:e233-e239
Introduction Down syndrome (DS) is the most common chromosomal disorder. It is accompanied by several comorbidities, which could lead to severe morbidity and mortality. Congenital heart disease (CHD) is one of the most commonly described condition. O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8f519c367843c620390f7c1d9b782d0
https://doi.org/10.1055/s-0041-1735537
https://doi.org/10.1055/s-0041-1735537
Autor:
Hoda M Abd El-Ghany, Iman Ehsan Abdel Meguid, Rabab El Hawary, Safa Meshaal, Iman Taha Lafy Shimila, Eman Roshdy Radwan
Publikováno v:
Laboratory medicine. 53(4)
Objective Recurrent infection in Down syndrome (DS) has been previously documented; the potential role of platelets and neutrophil-platelet interaction has not been addressed in previous studies. Patients and Methods Using flow cytometry, we evaluate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88b78b784cc97d8fd0aae7d72c933b07
https://pubmed.ncbi.nlm.nih.gov/35285899
https://pubmed.ncbi.nlm.nih.gov/35285899
Autor:
Nihal AlMenabawy, Hebatallah M Hassaan, Manal Ramadan, Iman Ehsan Abdel Meguid, Hala Ahmed El Gindy, Christian Beetz, Laila Selim
Publikováno v:
Mitochondrion. 65
Mitochondrial DNA (mtDNA) depletion syndromes (MDS) are a heterogeneous group of rare autosomal recessive genetic disorders characterized by a decrease in the number of mtDNA copies inside the organ involved. There are three distinct forms of MDS inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7699498b64e4201ac75d9406368be165
https://pubmed.ncbi.nlm.nih.gov/35750291
https://pubmed.ncbi.nlm.nih.gov/35750291
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 14, No 3 (2013); 307–310
In Down syndrome (DS), trisomy 21 leads to overexpression of gene coding for specific enzymes. This overexpression translates directly into biochemical aberrations that affect multiple interacting metabolic pathways which culminates in cellular dysfu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc7702ba1b144251361f8f2a164930ef
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 14, No 2 (2013)
It is hypothesized that Down syndrome (DS) patients are associated with abnormalities of the immune system. Accordingly, this study was conducted to measure replicative aging and apoptosis in lymphocytes, which play an important role in the immune sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47c5d1f3d98fd4d1eb3c30083b33abfa
https://doi.org/10.1016/j.ejmhg.2013.01.001
https://doi.org/10.1016/j.ejmhg.2013.01.001
Publikováno v:
Journal of Pediatrics & Neonatal Care. 4
Background: Sepsis represents the main cause of mortality at intensive care units, with mortality rates from 30–50%. Elderly, pediatric, and immune-compromised patients show atypical clinical manifestations of bacterial infection. Several studies s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b032b22c6c75714e517a826367231d5a
https://doi.org/10.15406/jpnc.2016.04.00156
https://doi.org/10.15406/jpnc.2016.04.00156
Autor:
Nadia Badrawi, Mohamed Ghawas, Hany Aly, Iman Ehsan Abdel-Meguid, Tarek A. Hammad, Wael Lotfy
Publikováno v:
American Journal of Perinatology. 24:267-270
The purpose of this study was to evaluate the feasibility of the use oral ibuprofen suspension (OIS) in the treatment of patent ductus arteriosus (PDA) in premature infants. Premature infants (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b067b29526c3e9bed791cdd11159244
https://doi.org/10.1055/s-2007-976550
https://doi.org/10.1055/s-2007-976550
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 14, No 1 (2013); 55–62
On the trisomy Down syndrome Critical Region (DSCR1) is located the APP gene, which accelerates amyloid peptide protein (APP) expression leading to cerebral accumulation of APP-derived amyloid-beta peptides (Ab) and age-dependent cognitive sequelae.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdc2545fea1d4cbee02adb1837d849f7