Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Hadeel M. Abdelrahman"'
Publikováno v:
Minerva pediatrics.
Background Assessment of the left ventricular function in the dialysis children and explore its association with vitamin D level and markers reflecting calcium and phosphate metabolism. Methods In this case-control study, we enrolled forty children o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17833aec5bda4341f6be8c2925892079
https://pubmed.ncbi.nlm.nih.gov/34098711
https://pubmed.ncbi.nlm.nih.gov/34098711
Autor:
Doaa M. Abd Elrahman, Laila M. Sherief, Hadeel M. Abdelrahman, Hosam F. Elsaadani, Randa H. Mohamed, Ashgan A. Alghobashy
Publikováno v:
Human Immunology. 77:682-686
Background Type 1 diabetes mellitus (T1D) is a T cell-mediated autoimmune disease characterized by the destruction of pancreatic β cells. PTPN22 and IL2RA polymorphisms have been found to be associated with several autoimmune diseases including T1D.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd8817e368b85d36d23ade95ab8deb9e
https://doi.org/10.1016/j.humimm.2016.06.006
https://doi.org/10.1016/j.humimm.2016.06.006
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 1, Pp 67-72 (2015)
The aim of this work is to study the incidence of acute kidney injury (AKI) in neonates admitted to the neonatal intensive care unit (NICU) over a six-month period from September 2011 to March 2012. This prospective study was performed on 250 neonate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b65c69bbe5d072a245f267d868521bcc
http://www.sjkdt.org/article.asp?issn=1319-2442
http://www.sjkdt.org/article.asp?issn=1319-2442
Autor:
Doaa Mohammad, Hadeel M. Abdelrahman, Rehab A. Karam, Nelly R. Abdel Fattah, Tamer Hassan, Haitham M. Hashim, Noha A. Rezk
Publikováno v:
Research in Developmental Disabilities. 34:2092-2097
Catechol-O-methyltransferase (COMT) plays an important role in the catabolism of brain dopamine and norepinephrine, which have been implicated in the pathogenesis of Autism spectrum disorder (ASD) as well as in other neuropsychatric disorders. We aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6faa680fa3d0e744f46480c885f9dcda
https://doi.org/10.1016/j.ridd.2013.04.002
https://doi.org/10.1016/j.ridd.2013.04.002
Autor:
Nelly R. Abdel Fattah, Khaled M. El-Gerby, Haitham M. Hashim, Nagda M Elmasry, Nermin R. Abdel Fattah, Tamer Hassan, Hadeel M. Abdelrahman
Publikováno v:
Research in Autism Spectrum Disorders. 7:541-548
Despite of the great efforts that move forward to clarify the pathophysiologic mechanisms in autism, the cause of this disorder, however, remains largely unknown. There is an increasing body of literature concerning neurochemical contributions to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67af35d7f6485ad14bab0ada92ebdb7c
https://doi.org/10.1016/j.rasd.2012.12.005
https://doi.org/10.1016/j.rasd.2012.12.005
Publikováno v:
Research in Autism Spectrum Disorders. 7:199-204
It has been recently shown that dysregulation of transforming growth factor-β1 (TGF-β1), IL-23 and IL-17 has been identified as a major factor involved in autoimmune disorders. Based on the increasing evidence of immune dysfunction in autism the ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fecb1091ee4ed427732a4d1b20f9443
https://doi.org/10.1016/j.rasd.2012.08.007
https://doi.org/10.1016/j.rasd.2012.08.007
Publikováno v:
Egyptian Journal of Ear, Nose, Throat and Allied Sciences. 12(2):105-114
Introduction The detection of risk factors of hearing function is a crucial element for early intervention. Many researchers reported that protein energy malnutrition (PEM) and iron deficiency anemia affect myelination and neural maturation of the au
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24aeaa9cfde102ac94c308da9c920e7b
Autor:
Usama El-Safy, Ahmed Al-Akhras, Mohamed Hosam Mourad, Joaquin Brintrup, Tamer Hassan, Marwa Zakaria, Elisabeth Kohne, Hadeel M. Abdelrahman, M. A. Badr
Publikováno v:
Biomedical reports. 4(6)
In β-thalassemia, certain mutations cause a complete absence of β-globin chain synthesis, termed β 0 -thalassemia, while others may allow certain β-globin production and are termed β + - or β ++ -thalassemia. The homozygous state results in sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::469ed41d3db9f6d4a5993a790a30fe48
https://pubmed.ncbi.nlm.nih.gov/27284414
https://pubmed.ncbi.nlm.nih.gov/27284414
Autor:
Mohamed A. A. Almalky, Rehab S. Abdul-Maksoud, Hadeel M. Abdelrahman, Sanaa M. Abdelsalam, Sally M. Shalaby
Publikováno v:
Annals of allergy, asthmaimmunology : official publication of the American College of Allergy, Asthma,Immunology. 116(1)
Background The ADAM family is involved in some pathologic processes, such as inflammation and asthma. Objectives To assess the association between ADAM33 and ADAM12 single-nucleotide polymorphisms (SNPs) with asthma risk and severity and to investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723edb431845397de27f76f5bfcb034e
https://pubmed.ncbi.nlm.nih.gov/26553447
https://pubmed.ncbi.nlm.nih.gov/26553447
Autor:
Hadeel M. Abdelrahman, Naglaa M. Kamal, Marwa Zakaria, Besheir Abdalla Hassan, Laila M. Sherief
Publikováno v:
Hemoglobin. 39(2)
β-Thalassemia (β-thal) is the most common hereditary anemia in humans. With improvement of treatment protocols, patients are living longer and new complications have emerged. Few articles have reported the occurrence of malignancies among patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6da53d72ec03e558803def95ae53c959
https://pubmed.ncbi.nlm.nih.gov/25707677
https://pubmed.ncbi.nlm.nih.gov/25707677