Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Salam Al Kindi"'
Autor:
Mohamed A. Yassin, Mona Al-Rasheed, Murtadha Al-Khaboori, Mahmoud Marashi, Hani Osman, Yasser Wali, Salam Al Kindi, Faisal Alsayegh, Drew Provan
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
IntroductionThrombopoietin-receptor agonist (TPO-RAs) currently represent the state of art for treating immune thrombocytopenia. Their different molecular structures contribute to the difference in their pharmacodynamics and pharmacokinetics. This na
Externí odkaz:
https://doaj.org/article/4f6a087b656b418f86cf0903c7502c43
Autor:
Vaidyanathan Gowri, Tamima Al Dughaishi, Deepti Geetha, Marwa Al Riyami, Radhiya Alburaidi, Salam Al Kindi
Publikováno v:
Asian Journal of Transfusion Science, Vol 18, Iss 1, Pp 144-147 (2022)
Sickle cell anemia (SCA) is a multisystem disease, associated with increased risk for infection and thromboembolic disease, and pregnancy is a stressor for patients with SCA. In general, coronavirus disease 2019 (COVID-19) infection in SCA is associa
Externí odkaz:
https://doaj.org/article/bd3bb4148bea4474ae28310c3b790e32
Autor:
Issa Al Salmi, Ehab Mohammed, Salam Al Kindi, Muhanna Al Musalhi, Mohammed Al Ghonaim, Faisal Shaheen, Suad Hannawi
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 33, Iss 4, Pp 586-592 (2022)
Graft versus host disease (GVHD) occurs quite often after hematopoietic cell transplantation. However, it is a rare complication after solid organ transplantation and consists of a reaction of donor-derived immune cells directed against host tissues,
Externí odkaz:
https://doaj.org/article/038aea44dcf34570ae5da56cbea3ee40
Autor:
Murtadha Al-Khabori, Faisal Alsayegh, Hasan Al Yaseen, Sabir Hussien, Amar Lal, Muna Al Rasheed, Mohammad Al Bader, Salam Al Kindi, Mahmoud Marashi
Publikováno v:
Oman Medical Journal, Vol 37, Iss 4, Pp e407-e407 (2022)
Acquired thrombotic thrombocytopenic purpura (aTTP) is a rare hematological emergency characterized by microangiopathic hemolytic anemia, thrombocytopenia, fever, and multiorgan failure due to autoimmune-mediated deficiency in ADAMTS-13 activity. Cur
Externí odkaz:
https://doaj.org/article/63db538f393542d889941968e47f1c23
Autor:
Arwa Z. Al-Riyami, Yahya Al-Kindi, Jamal Al-Qassabi, Sahimah Al-Mamari, Naglaa Fawaz, Murtadha Al-Khabori, Mohammed Al-Huneini, Salam Al Kindi
Publikováno v:
Oman Medical Journal, Vol 37, Iss 4, Pp e405-e405 (2022)
We aimed to estimate the nature and prevalence of paroxysmal nocturnal hemoglobinuria (PNH) among Omani patients. We performed a retrospective review of all patients who were tested for PNH by flow cytometry at the Sultan Qaboos University Hospital,
Externí odkaz:
https://doaj.org/article/faadf04baa3f4600a93ec2f2260a4a0a
Publikováno v:
Oman Medical Journal, Vol 33, Iss 4, Pp 322-330 (2018)
Objectives: We conducted this study to assess the risk factors of gestational anemia and evaluate the effectiveness of a culturally-tailored nutrition educational intervention on hemoglobin (Hb) status among pregnant Omani women. Newborn birthweight
Externí odkaz:
https://doaj.org/article/a17d118a05534f2cb5672bb28f1125b1
Autor:
Abdul Kareem Almomen, Abdul Ghani Al Bakistani, Ahmad Alsaeed, Asma Al Olama, Ayman Hejazi, Christian Awarji, Fahed Almhareb, Faisal Alsayegh, Hazzaa Alzahrani, Mahmoud Almarashly, Mohammad Qari, Mohammad Aslam, Rania Seliem, Salam Al Kindi, Saud Abuharbesh, TareK Owaidah, Wafaa Bassuni
Publikováno v:
Journal of Applied Hematology, Vol 5, Iss 2, Pp 37-44 (2014)
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired, rare clonal blood disorder, characterized by chronic intravascular hemolysis, bone marrow failure, renal failure and pulmonary hypertension, and a heightened risk of thrombotic complications.
Externí odkaz:
https://doaj.org/article/1d3ae7270fca4498a20fca0b3ea5edee
Publikováno v:
Oman Medical Journal, Vol 28, Iss 3, Pp 207-209 (2013)
We report here four cases of genital ulcers that developed after the administration of all-trans retinoic acid (ATRA) for the treatment of acute promyelocytic leukemia (APL). Between October 2007 and March 2010, three males and one female (age range
Externí odkaz:
https://doaj.org/article/43802748a4914a788bb76a3ce2f77ee8
Autor:
Ekaterina Yu. Chelysheva, Anna Turkina, Jane F. Apperley, Mohamed A Yassin, Delphine Rea, Franck E. Nicolini, Daniela Barraco, Konstantin Kotlyarchuk, Khamida Kazakbaeva, Sukhrob Saliev, Adi Shacham, Dong-Wook Kim, Salam Al-Kindi, Penka Ganeva, Roman Shmakov, Jennifer Byrne, Harry Robertson, Cerrano Marco, Evgenia Polushkina, Malgorzata Monika Trawinska, Elisabetta Abruzzese
Publikováno v:
Blood. 140:1498-1500
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