Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Melanie Tauro"'
Autor:
Jamal Al Qassabi, Saif Al Hosni, David Dennison, Abdulhakim Al Rawas, Rupert Handgretinger, Melanie Tauro, Shoaib Al Zadjali, Salem Al Tamemi, Hanan F. Nazir, Ibtisam Elnour
Publikováno v:
Transplantation and Cellular Therapy. 27:881.e1-881.e5
Autosomal recessive complete INF-γ receptor-2 (IFN-γR2) deficiency is a rare, potentially fatal primary immune deficiency that predisposes to disseminated mycobacterial disease. Hematopoietic stem cell transplantation (HSCT) is currently the only c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9a5cd3bac87a21bc251f497ce3b85c1
https://doi.org/10.1016/j.jtct.2021.07.013
https://doi.org/10.1016/j.jtct.2021.07.013
Autor:
Khalil Al-Farsi, Bushra Salman, David Dennison, Mohammed Al-Huneini, Melanie Tauro, Salam Alkindi, Abdulhakeem Al-Rawas, Mohammed Al-Za'abi, Murtadha Al-Khabori
Publikováno v:
Hematology/Oncology and Stem Cell Therapy, Vol 10, Iss 2, Pp 70-78 (2017)
Busulfan (Bu)-based preparative regimens in hematopoietic stem cell transplantation are commonly used. Previous studies have shown that Bu at a fixed dose of 3.2 mg/kg/day (FBD) given intravenously decreases variability in drug pharmacokinetics and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f82d4a6b9d1d09c04248f651f983143
https://pubmed.ncbi.nlm.nih.gov/28408108
https://pubmed.ncbi.nlm.nih.gov/28408108
Autor:
A T Al Lawatia, S. Al Kindi, S. Al Zadjali, Fehmida Zia, J Ur Rehman, Shyam Sunder Ganguly, Melanie Tauro, A Alghazaly, Muhammad Irfan Khan, Anil Pathare, David Dennison, Shahina Daar, Nadeem Nusrat, Hammad Khan
Publikováno v:
Bone marrow transplantation. 42
Hematopoietic SCT (HSCT) is an integral part of the management of patients with hematologic disorders. The Sultanate of Oman, with a population of 2.3 million, has an HSCT program based in the Sultan Qaboos University (SQU) hospital. Initiated in 199
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2c3379d393d906a2ad190e88540221e
https://pubmed.ncbi.nlm.nih.gov/18724280
https://pubmed.ncbi.nlm.nih.gov/18724280
Autor:
Yusra Al Habsi, Rahma Al Mahrizi, Aqeela Al Lawati, David Dennison, Khalil Al Farsi, Abdulhakeem Al Rawas, Mohammed Al Huneini, Salam Al Kindi, Arwa Z. Al Riyami, Shoaib Al Zadjali, Rhea Misquith, Melanie Tauro, Pathare Anil, Rajagopal Krishnamoorthy, Maryam Al Shukri, Murtadha Al Khabori
Publikováno v:
Biology of Blood and Marrow Transplantation. 19(2):S285-S286
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d5ef197614a729641155b1174a33db9
Autor:
J. David Dennison, R. Krishnamoorthy, Shyam Sunder Ganguly, Shoaib Al Zadjali, Krishnaratnam Kannan, Shanmugakonar Muralitharan, Anil Pathare, Maria Lourdes Macalalad, Salam Al Kindi, Melanie Tauro, Aqueela Taqi Al Lawatia
Publikováno v:
Blood. 106:2740-2740
Permanent alopecia (PA) is an important complication of allogeneic bone marrow transplantation (BMT). In an analysis of 30 consecutive Omani children who underwent BMT in this center, we have previously reported a strong association between high syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c1de6dd0d381dac67f0e68b44cc7176
https://doi.org/10.1182/blood.v106.11.2740.2740
https://doi.org/10.1182/blood.v106.11.2740.2740
Autor:
Shoaib Al Zadjali, J. David Dennison, Shahina Daar, Anil Pathare, Marie-Helene Quernin, Krishnaratnam Kanan, Salam Al Kindi, Shyam S. Ganguly, R. Krishnamoorthy, Shanmugakonar Muralitharan, Evelyne Jacqz-Aigrain, Melanie Tauro
Publikováno v:
Blood. 104:1149-1149
Bone marrow transplantation is the only curative treatment modality available for patients with homozygous beta thalassemia. Although the transplant outcome for good-risk patients is uniformly excellent, rejection continues to remain a serious compli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa40a8d913d27e16504c9bccc949e68e
https://doi.org/10.1182/blood.v104.11.1149.1149
https://doi.org/10.1182/blood.v104.11.1149.1149