Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Durjoy K. Shome"'
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-21 (2023)
Abstract Bone marrow fibrosis represents an important structural change in the marrow that interferes with some of its normal functions. The aetiopathogenesis of fibrosis is not well established except in its primary form. The present review consolid
Externí odkaz:
https://doaj.org/article/8ab7ec0c571a42e28cfa56093160d792
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 21:S261-S262
Introduction: In ALL, current drug efficacy studies focus on reducing leukemia cell burden. However, if drugs have limited effects on LSCs, these cells may expand and eventually cause relapse. The experimental anti-leukemic drug parthenolide (PTL) ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8f6a508e3ad3b53e94e7b2f5a38d757
https://doi.org/10.1016/s2152-2650(21)01639-6
https://doi.org/10.1016/s2152-2650(21)01639-6
Autor:
Durjoy K. Shome, Ali S Sinan, Ali Ebrahim, Kameela S. Majed, Eman J Mansoor, Ahmed A. Jaradat, Ahmed I Mahozi, Sheikh Abdul Azeez Pasha, Mohammad S Ebraheem, Mohammed Alrahim
Publikováno v:
Indian Journal of Critical Care Medicine : Peer-reviewed, Official Publication of Indian Society of Critical Care Medicine
Background and Aims: In sickle cell disease (SCD) patients admitted for intensive care, evaluation of platelet counts in different types of sickle cell complications and its prognostic relevance are not well-studied. Illuminating these aspects were t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d339298340d274650d064d0aa13c5edd
https://doi.org/10.4103/ijccm.ijccm_49_18
https://doi.org/10.4103/ijccm.ijccm_49_18
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 33:545-551
In this study, the potential effect of three HFE gene polymorphisms (C282Y, H63D and S65C) and the SLC40A1 A77D polymorphism on iron balance was investigated in 234 subjects (91 Arab beta-thalassemia major (BTM) patients, 34 beta-thalassemia trait (B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b95d4ce10fb9f04d32e67acca12f2bb
https://doi.org/10.1007/s12288-016-0775-7
https://doi.org/10.1007/s12288-016-0775-7
Autor:
Ameera A. Radhi, K. A. Sharif, S. Abuamer, A. Al-Asheeri, Durjoy K. Shome, Ahmed A. Jaradat, J. P. Bapat, A. Al-Ajami, J. Al-Touq
Publikováno v:
International Journal of Laboratory Hematology. 39:76-83
SummaryIntroduction Bahrain has high prevalence rates of sickle cell and thalassemia in the population. This study reports the frequencies and phenotypic characteristics of α- and/or β-thalassemia associated with sickle-cell disease (SCD) in a tert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4053c50ff39fc68fcdace92a8b1b94
https://doi.org/10.1111/ijlh.12577
https://doi.org/10.1111/ijlh.12577
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 32:104-109
Hydroxyurea (HU) is used as a disease-modifying agent in sickle cell disease (SCD). Its beneficial effects have been ascribed to inhibition of the sickling process through increase of fetal hemoglobin (HbF) levels and influence on multiple factors af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0de68e5df79739e082c64f008f44223
https://doi.org/10.1007/s12288-015-0529-y
https://doi.org/10.1007/s12288-015-0529-y
Publikováno v:
Annals of Hematology. 92:509-515
Thrombotic microangiopathy (TMA) in patients with sickle cell disease (SCD) is a rare complication. These patients manifest microangiopathic hemolytic anemia (MAHA) with laboratory evidence of hemolytic anemia, schistocytosis, and thrombocytopenia. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8950bd419d6942e0efd37e2a84410c12
https://doi.org/10.1007/s00277-012-1647-3
https://doi.org/10.1007/s00277-012-1647-3
Autor:
Abdel Halim Salem, Suad Al Fadhli, Rashed Al Bannay, Durjoy K. Shome, Aliaa Al Azme, Ahmed A. Jaradat
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 26(8)
Thrombomodulin is expressed on endothelial cells and monocytes (mTM) where it has an anticoagulant function. Enzymatic cleavage from the cell surface produces soluble thrombomodulin (sTM) in plasma. Abnormal levels of sTM and mutations in the thrombo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd51a4811091babc22ac68a273610fd5
https://pubmed.ncbi.nlm.nih.gov/26226255
https://pubmed.ncbi.nlm.nih.gov/26226255
Autor:
Durjoy K. Shome, Abdulla Al Ajami, Radha K. Dhiman, Phillip I. Tarr, Bernard S. Kaplan, Hyat Al Mahroos, Srdjan Jelacic, Ali Albaqali, Ahmed Al Arrayed, Afaf Jamsheer, Adel Ghuloom
Publikováno v:
American Journal of Kidney Diseases. 41:709-713
Background: Hemolytic uremic syndrome (HUS) has been associated with typhoid fever caused by Salmonella typhi . The pathogenesis of HUS in the context of S typhi infection is not known. The authors report on a patient with typhoid fever in whom HUS a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08d0be1c04a3e4ca68f650c540f050b3
https://doi.org/10.1053/ajkd.2003.50135
https://doi.org/10.1053/ajkd.2003.50135
Autor:
Robert C. Stern, Blanca Vicandi, Kazue Asakawa, Takahiro Kasamatsu, Harumi Kamaguchi, Ahmad Reza Shamshiri, Hirohiko Sakamoto, Eiji Ohno, Leo B. Twiggs, Elenice Kraemer Morais, Toshitaka Uehara, Mehrangiz Rahmani, Bernard Naylor, Deborah Witte, Farrokh Saidi, Ibrahim Ramzy, Mai Gu, Mark Schiffman, Michiko Takahashi, Waddah Eskaf, Koichi Tamura, Stefan E. Pambuccian, Naveen C. Bhatt, Patricia E. Saigo, Robyn L. Gaffney, Dilip K. Das, Nancy E. Joste, Antoon Philippi, Payam Razavi, Mahmoud EL-Sayed, Nim Lai Wong, Alireza Sepehr, Luan D. Truong, Leslie G. Dodd, Hiroyuki Kuramoto, Ronaldo João S. Torresini, Gary J. Bachowski, Douwe Remerij, Pirooz Salehian, Angela Krul, Maria Schrik, Wolfgang Behnisch, Howard T. Thaler, Yukihiro Murase, Luíz Fernando Jobim, Miyuki Matubara, Richard R. Barakat, Mary L. Ostrowski, Durjoy K. Shome, Pranab Dey, Martin Griesshammer, Markus Bangerter, Kusum Kapila, Ada R.S. Diehl, G. Peter Vooijs, Munehiro Yokoyama, Manabu Hattori, Elena Adrianza, Katharine Liu, Richard M. Feddersen, Bep van’t Hof, João Carlos Prolla, Dawoud Abdel-Rahman El-Halabi, Thèrése Bocklage, Jett R. Brady, Marcel Mravunac, Weiji Shi, Kusum Verma, Jehoram T. Anim, Suk King Wan, Selina Bhattarai, Pilar López-Ferrer, Sachiko Nagai, Yoshio Kuwashima, Frank Smedts, Yuichi Sugisaki, Haruaki Satoh, José M. Viguer, Yasuhiko Watarai, Anju Garg, Iling Chen, Kenji Shiromizu, B. Rath, Luis Ortega, Cees van Heusden, José A. Jiménez-Heffernan, Go Kimura
Publikováno v:
Acta Cytologica. 44:703-708
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b3a4e6b4aeed1d18a16875cc6bebcd5
https://doi.org/10.1159/000328552
https://doi.org/10.1159/000328552