Zobrazeno 1 - 10
of 21
pro vyhledávání: '"AbdulRahman Al-Musa"'
Autor:
Mahasen Saleh, Abdullah Al-Jefri, Saadiya Khan, Khawar Siddiqui, Muhammed Ameen, Abdulrahman Al-Musa
Publikováno v:
Journal of Hematology
Background: Essential thrombocythemia (ET) is one of the “classic” Philadelphia chromosome negative (Ph-) myeloproliferative neoplasms characterized by sustained thrombocytosis, increased megakaryopoiesis and high risk of vascular complications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::414f22345be225aa2cc54a0fdd7dbfcb
https://doi.org/10.14740/jh822
https://doi.org/10.14740/jh822
Autor:
Batoul Baz, Dorota Monies, Thamer A Alamoudi, Ahmed Tarawah, Nouf S Al-Numair, Mahasen Saleh, Nada Al Tassan, Hala AbaAlkhail, M. Abouelhoda, Randa AlNounou, Hazza Alzahrani, Abdulrahman Al-Musa, Rahaf Altahan, Amjad Jabaan, Basma Al Abdulaziz, Tarek Owaidah
Publikováno v:
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-7 (2019)
NPJ Genomic Medicine
NPJ Genomic Medicine
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder. Around 490 mutations in ITGA2B and ITGB3 genes were reported. We aimed to use targeted next-generation sequencing (NGS) to identify variants in patients with GT. We screen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0ca044888b0a091b31dba2f34499d67
http://link.springer.com/article/10.1038/s41525-019-0079-6
http://link.springer.com/article/10.1038/s41525-019-0079-6
Autor:
H. Al Zahrani, H. Masmali, Abdulmajeed Albanyan, Tarek Owaidah, Randa Alnounou, A. Malik, A. AlJefri, Mahasen al Saleh, Abdulrahman Al-Musa, R. Nasr
Publikováno v:
International Journal of Laboratory Hematology. 37:503-508
Glanzmann thrombasthenia (GT) is a rare inherited platelet disorder that is characterized by spontaneous or postprocedural bleeding. The diagnosis of GT depends on identifying the dysfunction of the platelets.The aim of this study was to compare a wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::affae2a0b63fbfe3c021c8d0b34f93c1
https://doi.org/10.1111/ijlh.12320
https://doi.org/10.1111/ijlh.12320
Autor:
Amal Al-Seraihy, Ashraf Khairy, Abdulrahman Al-Musa, Hasan Shahin, Samer Markiz, Mouhab Ayas, Hassan El-Solh, Abdullah Al-Jefri, Khawar Siddiqui, Ali Al-Ahmari
Publikováno v:
Biology of Blood and Marrow Transplantation. 20(10):1599-1603
Hematopoietic cell transplantation (HCT) can cure bone marrow failure in patients with Fanconi Anemia (FA), and it is generally accepted that these patients should receive low-intensity conditioning because of the underlying DNA repair defect in thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac0a1d83f561540585f33a66f9d2edd
Autor:
Abdullah Al-Jefri, Ibrahim Al-Ghemlas, Khawar Siddiqui, Samer Markiz, Mouhab Ayas, Hasan Shahin, Hassan El-Solh, Amal Al-Seraihy, Abdulrahman Al-Musa, Mahasen Saleh, Ali Al-Ahmari, Ashraf Khairi
Publikováno v:
Biology of Blood and Marrow Transplantation. 22(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6d3cec0d161fb057b68e658c61ad8f5
Autor:
Abdulrahman Al Musa, Mahasen Saleh, Iman M Zaghloul, Eman E Al Obary, Abdulrazaq Al-Jazairi, Zohair Al-Halees
Publikováno v:
Asian Cardiovascular and Thoracic Annals. 20:153-159
Current dosing guidelines for unfractionated heparin therapy in pediatric patients are based on recommendations of only one study that evaluated a weight-based dosing nomogram. To test the hypothesis that adhering to a strict weight-based nomogram yi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be874c665b1e116f9db307ade13609cd
https://doi.org/10.1177/0218492311434646
https://doi.org/10.1177/0218492311434646
Autor:
Abdullah Al-Jefri, Hassan El-Solh, Abdulrahman Al-Musa, Asim F. Belgaumi, Mohammed Osman, M Al-Mahr, Mahasen Saleh, Layla Osman, Mohammed F. Salim, Mohammed Al-Bakrah
Publikováno v:
Cancer. 97:2898-2903
BACKGROUND The goals of the current study were to examine the incidence and severity of toxicity resulting from dexamethasone and prednisone during induction therapy for children with precursor B-cell acute lymphoblastic leukemia (ALL) and to determi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be93466d03d98c63915c6f393264440b
https://doi.org/10.1002/cncr.11390
https://doi.org/10.1002/cncr.11390
Autor:
Mahmoud Abu-Riash, Tarek Owaidah, Ali Al-Omari, Hazzaa Alzahrani, Abdulkareem Al Momen, Mahasen Saleh, Fahad Alothman, Fawaz Alkasim, Abdulrahman Al-Musa, Said Y Mohamed, Khawar Siddiqui, Randa Al Nouno, Mansor Ahmed, Ahmed Tarawah, Fatima Al Batniji, Saud Abu-Herbish
Publikováno v:
Medicine. 96:e5456
Hemophilia A and B are X-linked diseases that predominantly affect male patients. Patients can develop coagulation factor inhibitors, which exponentially increases the treatment cost. However, the prevalence of factor VIII and IX inhibitors in Saudi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbb0f6860e40275bc90a5e97ab205fce
https://doi.org/10.1097/md.0000000000005456
https://doi.org/10.1097/md.0000000000005456
Autor:
Hassan El-Solh, Asem Bukhari, Khawar Siddiqui, Amal Al-Seraihy, Asim F. Belgaumi, Abdulrahman Al-Musa, Mouhab Ayas, Ali Al-Ahmari
Publikováno v:
Leukemialymphoma. 54(3)
Results of second-line therapy for childhood acute lymphoblastic leukemia (ALL) remain suboptimal, particularly for high-risk groups identified using timing and site of relapse. We report results of prospectively collected data for pediatric patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63153c48e8b22a42c03d0e2b48f980e9
https://pubmed.ncbi.nlm.nih.gov/22938053
https://pubmed.ncbi.nlm.nih.gov/22938053
Autor:
Abdulrahman Al Musa, Tarek Owaidah, Rubina J. Malik, Suleman Al-Sweedan, Sohaib Zulfiqar, Mahasen al Saleh, Rafat Jafri, Nicy Joseph, Hazzaa Alzahrani, Khawar Siddiqui
Publikováno v:
Blood. 124:5064-5064
BACKGROUND The rare coagulation disorders are heritable abnormalities of hemostasis that may present significant difficulties in diagnosis and management to hemophilia center clinicians. The common feature shared by these disorders is that their over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67904794b8b905128c112346c382ccfd
https://doi.org/10.1182/blood.v124.21.5064.5064
https://doi.org/10.1182/blood.v124.21.5064.5064