Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Shoaib Al Zadjali"'
Publikováno v:
Oman Medical Journal, Vol 39, Iss 1, Pp e592-e592 (2024)
Objectives: We sought to define the prevalence of isocitrate dehydrogenase (IDH) mutations, evaluate the clinicopathologic impact of IDH mutations, assess the effect of IDH mutations on the response to the currently offered treatment for acute myeloi
Externí odkaz:
https://doaj.org/article/4720ce149d544b38a3ee3644429a173a
Autor:
Salam Alkindi, Shoaib Al Zadjali, Mohamed Al Rawahi, Hamoud Al Haddabi, Shahina Daar, Refaat Abdullah Elsadek, Bahaa Eldeen Diab Sherkawy, Anil Pathare
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 13, Iss 1 (2021)
Abstract Hemoglobin La Desirade (Hb La Desirade) is an unstable hemoglobin variant characterized by amino acid Alanine (Ala) replacing Valine (Val) at position 129 (H7) in the beta chain. Hb La Desirade exhibits a decreased oxygen affinity and normal
Externí odkaz:
https://doaj.org/article/7a3093bc59dd4176ad153ffc2497e438
Publikováno v:
Haematologica, Vol 94, Iss 1 (2009)
Externí odkaz:
https://doaj.org/article/01c6ec5efa1a4f3390ed7460e393722f
Autor:
Intisar, Al-Riyami, Murtadha, Al-Khabori, Khalid, Al Balushi, Shoaib, Al-Zadjali, Mohammed, Al-Rawahi, David, Dennison, Mohammed, Al-Hunaini, Abdulhakeem, Al-Rawas, Mansour, Al-Moundhri
Publikováno v:
Therapeutic Drug Monitoring. 44:527-534
Busulfan (Bu) is an alkylating drug used in many preparative regimens before hematopoietic stem cell transplantation (HSCT). It is conjugated in the liver mainly by glutathione S-transferase isoenzyme A1-1 ( GSTA1 ). Genetic polymorphisms in these is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::838e5fb66566b5ac5a57d956debed96e
https://doi.org/10.1097/ftd.0000000000000957
https://doi.org/10.1097/ftd.0000000000000957
Autor:
Jalila Alshekaili, Iman Nasr, Mohammed Al-Rawahi, Zainab Ansari, Nasser Al Rahbi, Hamed Al Balushi, Shoaib Al-Zadjali, Mahmood Al Kindi, Almundher Al-Maawali, Matthew C. Cook
Publikováno v:
Clinical Immunology. 252:109646
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::410e6a5569d02c2bc4bb68e62e7cdaf7
https://doi.org/10.1016/j.clim.2023.109646
https://doi.org/10.1016/j.clim.2023.109646
Autor:
Salem Al-Tamemi, Shoaib Al-Zadjali, Zandre Bruwer, Shafiq-Ur-Rehman Naseem, Nabila Al-Siyabi, Mohammed ALRawahi, Khalsa Alkharusi, Khalid Al-Thihli, Fathiya Al-Murshedi, Abeer AlSayegh, Almundher Al-Maawali, David Dennison
Publikováno v:
Journal of clinical immunology.
Early identification of inborn errors of immunity (IEIs) is crucial due to the significant risk of morbidity and mortality. This study aimed to describe the genetic causes, clinical features, and survival rate of IEIs in Omani patients.A prospective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95f2c953298b61cdd542cc1b6a5bef1b
https://pubmed.ncbi.nlm.nih.gov/36324046
https://pubmed.ncbi.nlm.nih.gov/36324046
Autor:
Arwa Z. Al-Riyami, Ali Al Madhani, Shahina Daar, Salam Al Kindi, Mohammed Al Rawahi, Shoaib Al Zadjali, Yasser Wali
Publikováno v:
Hemoglobin. 44:20-26
α-Thalassemia (α-thal) is the most common autosomal recessive hemoglobinopathy. There is a vast diversity and geographical variability in underlying genotypes in Hb H (β4) patients. Herein, we describe the genotypes found in the largest report of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45d82236c979eda21310849ef8ad0db0
https://doi.org/10.1080/03630269.2020.1720709
https://doi.org/10.1080/03630269.2020.1720709
Autor:
Salam Alkindi, Anil Pathare, Ali Al-Madhani, Shoaib Al-Zadjali, Hamood Al-Haddabi, Qamariya Al- Abri, David Gravell, Mariam Mathew, Rajagopal Krishnamoorthy
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 11, Iss 4, Pp 462-469 (2011)
Objectives: The aim of this study was to validate the interpretation of red blood cell indices in complete blood count (CBC) and high performance liquid chromatography (HPLC) results on cord blood samples in consecutive Omani neonates. Methods: Cord
Externí odkaz:
https://doaj.org/article/d6374ecf546243b3bb8b2096686bf6de
Autor:
Dina Al Hinai, Shoaib Al-Zadjali, Arwa Z. Al-Riyami, Murtadha Al-Khabori, Mohammed Al-Rawahi, Saif Al-Hosni, Ali Al-Marhoobi, Gregory A. Denomme, Hamad Al-Riyami
Publikováno v:
Vox sanguinisREFERENCES. 117(3)
BACKGROUND AND OBJECTIVES Blood group genotyping has been used in different populations. This study aims at evaluating the genotypes of common blood group antigens in the Omani blood donors and to assess the concordance rate with obtained phenotypes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::159c54a598da8434af51988fe8a282a5
https://pubmed.ncbi.nlm.nih.gov/34647328
https://pubmed.ncbi.nlm.nih.gov/34647328
Autor:
Khalfan, Al Senaidi, Surekha, Maveda, Niranjan, Joshi, Hanan, Nazir, Mohamed, Elshinawy, Shoaib, Al Zadjali, Abdulhakim, Al Rawas, Islam, Elghamry, Yasser, Wali, Doaa, Khater
Publikováno v:
Acta bio-medica : Atenei Parmensis. 93(2)
Cardiac complications occur in patients with non-transfusion dependent thalassemia (NTDT). The study aimed to evaluate transfusion effect on systolic and diastolic cardiac function in young NTDT patients. Methods: Study design: Cohort study. Seventee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8b152c2a896ae5564c2b7a8042617fb4
https://pubmed.ncbi.nlm.nih.gov/35546036
https://pubmed.ncbi.nlm.nih.gov/35546036