Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Haitham Khogeer"'
Autor:
Ali AlAhmari, Haitham Khogeer
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-7 (2023)
Abstract Background Hemophagocytic lymphohistiocytosis is a life-threatening disease heralded by fever, cytopenia, hepatosplenomegaly, and multisystem organ failure. Its association with genetic mutations, infections, autoimmune disorders, and malign
Externí odkaz:
https://doaj.org/article/ae738735ac0b4117bfe1341fa1aef1d1
Autor:
Tarek Owaidah MD, Salwa Bakr MD, Nouf Al-Numair PhD, Hala AbaAlkhail PhD, Hazzaa Alzahrani MD, Mahasen Saleh MD, Haitham Khogeer MD, Ahmed Tarawah MD, Hadeel Akkad MD, Faisal Al-Allaf PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 29 (2023)
Establishing a national screening program for hemophilia patients is highly encouraged by the World Health Organization and the World Federation of Hemophilia. Hence, this study aimed to analyze the variant spectrum of F8 and F9 genes in Arab hemophi
Externí odkaz:
https://doaj.org/article/a915efd2ecf849689c48cc1393e88a04
Autor:
Salwa Bakr, Areej AlFattani, Randa Al-Nounou, Nasir Bakshi, Haitham Khogeer, Maha Alharbi, Nasser Almousa, Waleed Alomaim, Amelita Aguilos, May Almoshary, Tarek Owaidah
Publikováno v:
Annals of Saudi Medicine, Vol 42, Iss 3, Pp 191-203 (2022)
BACKGROUND: Laboratory hematological tests are widely used in clinical practice to assess health and disease conditions. Reference ranges provided by laboratory reports are considered the most authoritative medical tools to assist in the decision-mak
Externí odkaz:
https://doaj.org/article/7a3c6017cc0b4a85a825ff90fdc55477
Autor:
Tarek Owaidah, Salwa Bakr, Hala AbaAlkhail, Hazza Alzahrani, Mahasen Saleh, Abdulrahman Almusa, Nouf Al-Numair, Haitham Khogeer, Faisal Al-Allaf
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S28-S29 (2022)
Objective: Hemophilia A and B are X-linked recessive bleeding disorder caused by variants in the factor VIII (FVIII) and factor IX (FIX) genes. There is correlation between the type of mutation and clinical severity of these patients. Establishing na
Externí odkaz:
https://doaj.org/article/073db1e27c2e444eaecd89f7dd5c0ce1
Autor:
Maha Alamri, Ahmed M. Albarrag, Haitham Khogeer, Jehad alburaiki, Magid Halim, Reem S. Almaghrabi
Publikováno v:
Journal of Infection and Public Health, Vol 14, Iss 8, Pp 1013-1017 (2021)
Histoplasma is endemic in North and Central America. We describe a case of disseminated histoplasmosis in a heart transplant recipient outside the known endemic areas. A 68-year-old gentleman known to have dilated cardiomyopathy. He underwent left ve
Externí odkaz:
https://doaj.org/article/c4176e9a139541eda55ee3122a7bc52a
Publikováno v:
Journal of Applied Hematology, Vol 8, Iss 3, Pp 99-104 (2017)
Background: Beta thalassemias are a group of hereditary blood disorders that are characterized by reduction or complete absence of the β-globin chain synthesis due to mutations, affecting critical areas of the β-globin gene on the chromosome 11. Th
Externí odkaz:
https://doaj.org/article/eeb54ec94c0f4bcca3fd4d2dd74dda75
Autor:
Evgeniya Angelova, Charlene Audette, Yelena Kovtun, Naval Daver, Sa A. Wang, Sherry Pierce, Sergej N. Konoplev, Haitham Khogeer, Jeffrey L. Jorgensen, Marina Konopleva, Patrick A. Zweidler-McKay, L. Jeffrey Medeiros, Hagop M. Kantarjian, Elias J. Jabbour, Joseph D. Khoury
Publikováno v:
Haematologica, Vol 104, Iss 4 (2019)
The potential of CD123-targeted therapies in acute lymphoblastic leukemia/lymphoma remains largely unexplored. We examined CD123 expression levels in a large cohort of patients with acute lymphoblastic leukemia/lymphoma and assessed the in vitro impa
Externí odkaz:
https://doaj.org/article/06f028d2f45b400fa072b97577ee8cd0
Autor:
Magid Halim, Ahmed Albarrag, Reem S. Almaghrabi, Maha Alamri, Haitham Khogeer, Jehad alburaiki
Publikováno v:
Journal of Infection and Public Health, Vol 14, Iss 8, Pp 1013-1017 (2021)
Histoplasma is endemic in North and Central America. We describe a case of disseminated histoplasmosis in a heart transplant recipient outside the known endemic areas. A 68-year-old gentleman known to have dilated cardiomyopathy. He underwent left ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01e272d7cb6293948617ab8fb46d7739
https://doi.org/10.1016/j.jiph.2021.05.012
https://doi.org/10.1016/j.jiph.2021.05.012
Autor:
Haitham, Khogeer, Shatha, Altahan, Ali, Alrehaily, Aamir, Sheikh, Khalid, Awartani, Murad, Al-Kaff, Saleh, Saleh, Hazzaa, Alzahrani, Areej, Alfattani, Tarek, Owaidah
Publikováno v:
Annals of clinical and laboratory science. 51(4)
The antiphospholipid syndrome (APS) is an autoimmune disease that is characterized by thrombosis and/or pregnancy failure and associated with the presence of all or at least one of three standard antibodies (anti-phospholipid (aPL) antibodies, includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::18aea6476011aa5806be3f1cfc9d66e7
https://pubmed.ncbi.nlm.nih.gov/34452895
https://pubmed.ncbi.nlm.nih.gov/34452895
Autor:
Hagop M. Kantarjian, Nitin Jain, Elias Jabbour, Sanam Loghavi, Areej Al Fattani, Dawen Sui, Chi Young Ok, Peng Wei, Jeffrey L. Jorgensen, Andrés E. Quesada, Audrey Lamb, Joseph D. Khoury, Evgeniya Angelova, L. Jeffrey Medeiros, Peter Hu, Haitham Khogeer, Hong Yang, Haitham Rahman, Beenu Thakral, Rashmi Kanagal-Shamanna, Sherry Pierce
Publikováno v:
British Journal of Haematology. 186:538-548
The differential immunophenotypic characteristics of early T precursor (ETP) acute lymphoblastic leukaemia/lymphoma (ALL) remain incompletely characterized. The study group (n = 142) included 106 (74·7%) men and 36 (25·3%) women with a median age o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b8fe30a445058265539f079cb06acc
https://doi.org/10.1111/bjh.15960
https://doi.org/10.1111/bjh.15960