Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mohamed Al Huneini"'
Autor:
Mohamed-Rachid Boulassel, Abdal-Aziz Issa El-Hussain, Moataz Mohamed Hassan, Mohamed-Lamine Toumi, Sameha Merzoug, Zahra Al-Qarni, Hammad Khan, Zied Gaifer, Khalil Al-Farsi, Murtadha Al-Khabori, Mohamed Al Huneini, Salam Al-Kindi
Publikováno v:
Haematologica, Vol 103, Iss 10 (2018)
Externí odkaz:
https://doaj.org/article/946cede8186141e6adcde0e43876e473
Autor:
Kowthar S. Hassan, Arwa Z. Al-Riyami, Mohamed Al-Huneini, Khalil Al-Farsi, Murtadha Al-Khabori
Publikováno v:
Oman Medical Journal, Pp 135-137 (2014)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by low levels of the G6PD enzyme. It is present worldwide but with more prevalence in the Middle East and the Mediterranean areas. We report a case of s
Externí odkaz:
https://doaj.org/article/8e80334e408d456fb995cac8a564e740
Autor:
Murtadha Al-Khabori, Khalil Al-Farsi, Sahima Al-Mamari, Hajer Al-Geithi, David Dennison, Mohamed Al-Huneini, Salam Alkindi
Publikováno v:
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. 59(3)
Background Granulocyte colony stimulating factor (G-CSF) given for 4–6 days is commonly used for mobilization of allogeneic stem cell donors. The primary objective of this study is to compare the yield of stem cell mobilization, assessed using a su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ba996e2ed5d918b7c7d7a81ba746f2
https://pubmed.ncbi.nlm.nih.gov/31948917
https://pubmed.ncbi.nlm.nih.gov/31948917
Autor:
Moataz M. Hassan, Hammad Khan, Abdal-Aziz Issa El-Hussain, Mohamed Rachid Boulassel, Khalil Al-Farsi, Sameha Merzoug, Murtadha Al-Khabori, Zahra Al-Qarni, Zied Gaifer, Salam Alkindi, Mohamed-Lamine Toumi, Mohamed Al Huneini
Publikováno v:
Haematologica. 103(10)
Recently, in vitro studies using progenitor-derived erythroid cells from normal individuals or sickle cell disease (SCD) patients, have identified metformin, an oral hypoglycemic drug, as a promising agent to increase fetal hemoglobin (HbF) levels.[1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a816d73db4bf061ccd79c51d7f1ca6ec
https://pubmed.ncbi.nlm.nih.gov/29700169
https://pubmed.ncbi.nlm.nih.gov/29700169
Autor:
Shahina Daar, Abdulhakeem Al-Hashim, Murtadha Al-Khabori, Mohamed Al-Huneini, Khalil Al-Farsi, Nasser Al-Kemyani, Arwa Z. Al-Riyami
Publikováno v:
Transfusion and Apheresis Science. 50:95-98
Non-invasive hemoglobin estimation may increase the recruitment of blood donors. CO-oximetry hemoglobin estimation is a non-invasive method used to estimate the hemoglobin level. The primary objective of this study is to validate the pulse CO-oximetr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afeb70bf77e5771722b36176212b990c
https://doi.org/10.1016/j.transci.2013.10.007
https://doi.org/10.1016/j.transci.2013.10.007
Autor:
Murtadha Al-Khabori, Hamad Al-Riyami, Yasser Wali, Mohamed Al Huneini, Huda Al-Harrasi, Salam Alkindi
Publikováno v:
Blood. 134:4831-4831
Objectives: Sickle Cell Disease (SCD) is an inherited hemoglobinopathy with multiple complications including stroke. It is observed that siblings with SCD have an increased risk of stroke if there was a sibling in the family with SCD and stroke (Dris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e2d30d0d20dc948190e0310f2d24b7d
https://doi.org/10.1182/blood-2019-125038
https://doi.org/10.1182/blood-2019-125038
Autor:
Salam Alkindi, Muhanna Almusalhi, Mahdiya Al-Belushi, Murtadha Al-Khabori, Mohamed Al Huneini, Muna Al Tarshi, Mohamed Nasser Al-Rawahi, Iman Al Noumani, Shoaib Al-Zadjali, Al Lamki Sulayma, Khalid Al Hashmi, Khalil Al Farsi
Publikováno v:
Blood. 132:5489-5489
Introduction: Mutations in the epigenetic regulators are commonly found in myeloid disorders including Myeloproliferative Neoplasm (MPN). Primary myelofibrosis, dysplastic changes and severity of the disease were associated with the mutation load. Mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74744b7883f606ec7ae44f81284417a7
https://doi.org/10.1182/blood-2018-99-118546
https://doi.org/10.1182/blood-2018-99-118546
Autor:
Shahina Daar, Khalil Al-Farsi, Murtadha Al-Khabori, Abdulhakeem Al-Hashim, Zeba Jabeen, Nasser Al-Kemyani, Mohamed Al-Huneini, Arwa Z. Al-Riyami
Publikováno v:
International journal of laboratory hematology. 35(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd220dbdb84ed6a497dbaebebbbe3d3
https://pubmed.ncbi.nlm.nih.gov/23480669
https://pubmed.ncbi.nlm.nih.gov/23480669
Autor:
David Dennison, I. Al Mandhari, Shoaib Al-Zadjali, R. Al-Mahrizi, Mohamed Al-Huneini, Murtadha Al-Khabori, Khalil Al-Farsi, S. Alkindi, Abdulhakeem Al-Rawas
Publikováno v:
Biology of Blood and Marrow Transplantation. 17:S313
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3214973410f542dd5b9bb66b3f5bdbb2
https://doi.org/10.1016/j.bbmt.2010.12.475
https://doi.org/10.1016/j.bbmt.2010.12.475