Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ameera Bukhari"'
Autor:
Anas Alqurashi, Hatim Almaghrabi, Muath Alahmadi, Abdulaziz Alotaibi, Bandar Alotaibi, Abdulaziz Jastaniah, Ameera Bukhari, Mohammad Binhussein, Basant Othman, Amer Khojah
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-6 (2024)
Abstract Dry eye syndrome (DES) is a tear film disorder caused by increased tear evaporation or decreased production. The heavy workload on the eye and the increased usage of digital screens may decrease blink frequency, leading to an increased evapo
Externí odkaz:
https://doaj.org/article/55d255ab23af4f9f8846f9cb0a363e1c
Publikováno v:
Clinical Immunology Communications, Vol 5, Iss , Pp 26-29 (2024)
Syndrome of Congenital Sideroblastic Anemia, B-cell Immunodeficiency, Periodic Fevers, and Developmental Delay (SIFD) is caused by mutations in the tRNA nucleotidyltransferase 1 (TRNT1) gene. We present the case of a 13-month-old boy with development
Externí odkaz:
https://doaj.org/article/8ad89c70a12c43c8b1470024ea35c770
Autor:
Amer Khojah, Madeline Schutt, Gabrielle Morgan, Ameera Bukhari, Nicolas Bensen, Aaruni Khanolkar, Lauren M. Pachman
Publikováno v:
Clinical Immunology Communications, Vol 5, Iss , Pp 20-25 (2024)
This study investigates HLA-DR expression on activated T cells and serum neopterin levels in Juvenile Dermatomyositis (JDM) children pre- and post-treatment. Sixty-nine JDM children (less than 18 years) were included. Elevated HLA-DR+ T cells (>7 %)
Externí odkaz:
https://doaj.org/article/93727d4a8ec144cb81ec35aa79945c61
Publikováno v:
Clinical Immunology Communications, Vol 3, Iss , Pp 46-50 (2023)
X-linked inhibitor of apoptosis (XIAP) deficiency is a primary immunodeficiency associated with recurrent hemophagocytic lymphohistiocytosis (HLH) episodes. The clinical phenotypes of XIAP deficiency vary, ranging from splenomegaly to life-threatenin
Externí odkaz:
https://doaj.org/article/3785b88332f844799e4e08d028ef7bd5
Autor:
Ibrahim Alibrahim, Maria AlSulami, Turki Alotaibi, Ruba Alotaibi, Elaf Bahareth, Inam Abulreish, Sumayyah Alsuruji, Imad Khojah, Loie Goronfolah, Husni Rayes, Ameera Bukhari, Amer Khojah
Publikováno v:
Nutrients, Vol 16, Iss 16, p 2693 (2024)
(1) Background: Food allergy (FA) is an immune-mediated hypersensitivity to foods, significantly contributing to childhood morbidity and mortality. This study aimed to assess the prevalence, characteristics, and influencing factors of parent-reported
Externí odkaz:
https://doaj.org/article/6cc2c8d5cc6b47658ab9746b7455498c
Autor:
Amer Khojah, Lauren M. Pachman, Ameera Bukhari, Chi Trinh, Gabrielle Morgan, Surya Pandey, I. Caroline Le Poole, Marisa S. Klein-Gitelman
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 13, p 7126 (2024)
Juvenile Dermatomyositis (JDM) is the most common inflammatory myopathy in pediatrics. This study evaluates the role of Natural Killer (NK) cells in Juvenile Dermatomyositis (JDM) pathophysiology. The study included 133 untreated JDM children with an
Externí odkaz:
https://doaj.org/article/def0db7fa6364fde97d305ad9f9bd3d4
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-8 (2023)
Abstract Regulating B cell death is essential for generating antibodies and maintaining immune tolerance. B cells can die by apoptosis, and we report that human tonsil B cells, but not peripheral blood B cells also die by NETosis. This cell death is
Externí odkaz:
https://doaj.org/article/ab3587fb8d374b3da66d0cfb0d33e7b8
Publikováno v:
Clinical Immunology Communications, Vol 2, Iss , Pp 145-148 (2022)
IL-10 receptor (IL-10R) deficiency is a rare immune dysregulation disorder that is characterized by early-onset and life-threatening inflammatory bowel disease (IBD). Activation of the IL-10R inhibits the release of pro-inflammatory cytokines resulti
Externí odkaz:
https://doaj.org/article/d98d041596d4437b844862e1445e52ec
Autor:
Ameera Bukhari, Amer Khojah, Wilfredo Marin, Andrey Khramtsov, Galina Khramtsova, Christopher Costin, Gabrielle Morgan, Prathyaya Ramesh, Marisa S. Klein-Gitelman, I. Caroline Le Poole, Lauren M. Pachman
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 10553 (2023)
Otoferlin mRNA expression is increased in JDM patients’ PBMCs and muscle compared to healthy controls. This study aims to evaluate the role of otoferlin in JDM disease pathophysiology and its association with disease activity in untreated children
Externí odkaz:
https://doaj.org/article/fee98d5fa15a414f9455ee8190f840ea
Autor:
Amer Khojah, Hadeel Alshareef, Lujain Alzahrani, Mohammad Binhussein, Ameera Bukhari, Imad Khojah
Publikováno v:
Journal of Clinical and Experimental Hematology. 2:1-5
WHIM (Warts, Hypogammaglobulinemia, Infections, and Myelokathexis) syndrome is a rare primary immunodeficiency disorder characterized by susceptibility to human papillomavirus (HPV) infections, neutropenia, and hypogammaglobulinemia. WHIM syndrome is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4433e8f8ddc49a9214d3ea4f5532e9c
https://doi.org/10.46439/hematol.2.007
https://doi.org/10.46439/hematol.2.007