Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Noha A. Doudar"'
Autor:
Mohamed Abdelkader Morad, Noha A. Doudar, Nehad Tawfeek, Maha Yacoub, Taha Azoz, Doaa El Demerdash
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 4, Pp 352-359 (2024)
Introduction: Chronic immune thrombocytopenia (cITP) is characterized by dysregulation of the immune response. Until recently, the role of Th2-related cytokine gene polymorphisms was unclear. Interleukin 4 (IL-4) exerts its functions by binding to th
Externí odkaz:
https://doaj.org/article/47826fd59b5945ef81683e0dbead92d1
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 4, Pp 769-774 (2019)
Nephrotic syndrome (NS) is one of the most common kidney diseases seen in children. It is a disorder characterized by severe proteinuria, hypoproteinemia, hyperlipidemia, and generalized edema resulting from alterations of permeability at the glomeru
Externí odkaz:
https://doaj.org/article/6166dd47d9084553a121a15653fa557f
Publikováno v:
Egyptian Rheumatologist, Vol 44, Iss 3, Pp 251-255 (2022)
Aim of the work: To assess the effect of vitamin D receptor (VDR) polymorphism on lipid profile in patients with juvenile idiopathic arthritis (JIA) and study its relation to disease characteristics. Patients and methods: The study included 55 JIA ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d91a6656d76eef6a02d48252ff3a2d06
http://www.sciencedirect.com/science/article/pii/S1110116422000606
http://www.sciencedirect.com/science/article/pii/S1110116422000606
Publikováno v:
Medicine Science, Vol 7, Iss 2, Pp 347-9 (2018)
Sepsis is an important cause of neonatal death and perinatal brain damage, particularly in preterm infants. It is thought that activation of the inflammatory cascade triggered by cytokine may play a role in the pathogenesis of sepsis. Recent evidence
Externí odkaz:
https://doaj.org/article/f607d25a01094257838e58f444bafc5b
Autor:
Mohamed Abdelkader Morad, Noha A. Doudar, Nehad Tawfeek, Maha Yacoub, Taha Azoz, Doaa El Demerdash
Publikováno v:
Hematology, Transfusion and Cell Therapy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e19057e26f424eaccba937426f6323b
https://doi.org/10.1016/j.htct.2023.03.022
https://doi.org/10.1016/j.htct.2023.03.022
Autor:
Aya B Ahmed, Dina Ahmed Ezzat, Amna G Mabrouk, Noha A Doudar, Yasmen A Mohamed, Gamal Taha, Omnia Badawy
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e319-e323
Immune thrombocytopenia (ITP) is a multifactorial disease in which both environmental and genetic factors have been implicated. The study aimed to investigate a possible association of single nucleotide polymorphisms (SNPs rs266085 and rs2839693) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f7c1d4d9640d7706a77aad58d58420
https://doi.org/10.1097/mph.0000000000002342
https://doi.org/10.1097/mph.0000000000002342
Publikováno v:
Egyptian Rheumatologist, Vol 43, Iss 2, Pp 137-140 (2021)
Aim of the work: To investigate the association between IL and 16 genetic (rs4072111) single nucleotide polymorphism (SNP) and susceptibility to primary knee osteoarthritis (KOA) and to elaborate its connection with clinical and radiographic severity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d73378319bc12aebf77acebe7ca67f8
https://doi.org/10.1016/j.ejr.2020.12.003
https://doi.org/10.1016/j.ejr.2020.12.003
Publikováno v:
Egyptian Rheumatologist, Vol 42, Iss 1, Pp 35-39 (2020)
Aim of the work: A significant role of Leptin receptor (LEPR) is documented in inflammation, body weight homeostasis and maintenance of cartilage. This study was conducted to detect the existence of genetic association between Knee osteoarthritis (KO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1841194bb4aed0c9b1688d9ada69057d
http://www.sciencedirect.com/science/article/pii/S1110116419300523
http://www.sciencedirect.com/science/article/pii/S1110116419300523
Publikováno v:
Rheumatology, Vol 57, Iss 5, Pp 264-270 (2019)
Reumatologia
Reumatologia
ObjectivesMethyl-CpG-binding protein 2 (MECP2) and interleukin-1 receptor-associated kinase (IRAK1) are encoded by adjacent X-linked genes and recognized for their role in regulation of inflammation. The present case control study was conducted to de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::581f2707381dde7815b82e56fef4d04e
https://www.termedia.pl/Systemic-lupus-erythematosus-genetic-variants-in-Xq28-region,18,38503,1,1.html
https://www.termedia.pl/Systemic-lupus-erythematosus-genetic-variants-in-Xq28-region,18,38503,1,1.html
Association Study of FOXO3a Single-Nucleotide Polymorphism and Bronchial Asthma in Egyptian Children
Publikováno v:
The Egyptian journal of immunology. 27(1)
Asthma is the most common chronic illness in children and is a leading cause of childhood hospitalization and school absenteeism. Asthma presents with different phenotypes depending on age, gender, genetic background, environmental exposures and epig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::727fb271f8fbd85462e5058d77963d3c
https://pubmed.ncbi.nlm.nih.gov/33180382
https://pubmed.ncbi.nlm.nih.gov/33180382