Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Aisha Al Khinji"'
Autor:
Halima El Omri, Firyal Ibrahim, Ruba Yasin Taha, Riham Hassan Negm, Aisha Al Khinji, Mohammed Yassin, Ibrahim Al Hijji, Hanadi El Ayoubi, Hussein Baden
Publikováno v:
Turkish Journal of Hematology, Vol 27, Iss 04, Pp 289-293 (2010)
Acquired pure megakaryocytic aplasia is a rare hematological disorder characterized by thrombocytopenia with absent or markedly reduced megakaryocytes in the bone marrow. We report a case of a 25-year-old male diagnosed as acquired pure megakaryocyti
Externí odkaz:
https://doaj.org/article/24fb121830204a148c5e017ab1a1207b
Publikováno v:
Cancer Research. 81:3156-3156
Background: CEACAM6 is a cell adhesion receptor of the Ig-family over-expressed exclusively in primates and human pancreatic ductal adenocarcinoma (PDA). It is present in all subtypes and is enriched classical activated stroma subtype. CEACAM6 has mu
Publikováno v:
Journal of Clinical Oncology. 38:e16744-e16744
e16744 Background: Carcinoembryonic cell adhesion molecule 6 (CEACAM6) is a cell adhesion receptor of the Ig-superfamily overexpressed in human Pancreatic Ductal Adenocarcinoma (PDA), enriching to the classical activated stroma subtype. CEACAM6 has m
Autor:
Drazen Pulanic, Sunita Nathan, Khalid Tabbara, Gerhard C. Hildebrandt, Zack DeFilipp, Vaibhav Agrawal, Aditya Shreenivas, Pinki Prasad, Seth J. Rotz, Bronwen E. Shaw, Rafael F. Duarte, André Tichelli, Ami J. Shah, Erich Horn, Ibrahim Ahmed, Alicia Rovó, Nosha Farhadfar, Minoo Battiwalla, Amir Steinberg, Bipin N. Savani, Mary E.D. Flowers, Amer Beitinjaneh, Igor Petriček, Olaf Penack, Peiman Hematti, Grzegorz W. Basak, Hassan B. Alkhateeb, Robert Peter Gale, Michael Byrne, Neel S. Bhatt, Nuria Valdés-Sanz, Mahmoud Aljurf, Kristina Teär Fahnehjelm, Jean A. Yared, Ann A. Jakubowski, Natalie S. Callander, Raquel M. Schears, Jason Law, Ravi Pingali, Saurabh Chhabra, Linda J. Burns, Catherine J. Lee, Yoshihiro Inamoto, Dave Buchbinder, Asim Ali, Baldeep Wirk, Rammurti T. Kamble, Aisha Al-Khinji, Siddhartha Ganguly
Publikováno v:
Bone marrow transplantation
Biol Blood Marrow Transplant
Biol Blood Marrow Transplant
Non-graft-versus-host disease (GVHD) ocular complications are generally uncommon after hematopoietic cell transplantation (HCT) but can cause prolonged morbidity affecting activities of daily living and quality of life. Here we provide an expert revi
Autor:
Nosha Farhadfar, Baldeep Wirk, Rafael F. Duarte, Mary E.D. Flowers, Bronwen E. Shaw, Amer Beitinjaneh, Raquel M. Schears, Igor Petriček, Grzegorz W. Basak, Pinki Prasad, Michael Byrne, Siddhartha Ganguly, Yoshihiro Inamoto, Kristina Teär Fahnehjelm, Robert Peter Gale, Sunita Nathan, Alicia Rovó, Natalie S. Callander, Aisha Al-Khinji, Ann A. Jakubowski, Aditya Shreenivas, André Tichelli, Khalid Tabbara, Gerhard C. Hildebrandt, Rammurti T. Kamble, Drazen Pulanic, Peiman Hematti, Neel S. Bhatt, Minoo Battiwalla, Amir Steinberg, Dave Buchbinder, Linda J. Burns, Hassan B. Alkhateeb, Asim Ali, Catherine J. Lee, Jason Law, Ravi Pingali, Seth J. Rotz, Saurabh Chhabra, Nuria Valdés-Sanz, Ibrahim Ahmed, Olaf Penack, Ami J. Shah, Erich Horn, Zack DeFilipp, Mahmoud Aljurf, Vaibhav Agrawal, Jean A. Yared, Bipin N. Savani
Publikováno v:
Bone Marrow Transplantation. 54:782-783
In the original version of this article, author ‘Aisha Al-Khinji’ was incorrectly listed as ‘Aisha Ahmed’. This has now been corrected in both the PDF and HTML versions of the article to ‘Aisha Al-Khinji’.
Autor:
Halima El Omri, Mohammed Yassin, Riham Hassan Negm, Firyal Ibrahim, Hanadi R. El Ayoubi, Hussein Baden, Aisha Al Khinji, Ibrahim Al Hijji, Ruba Y. Taha
Publikováno v:
Turkish Journal of Hematology, Vol 27, Iss 04, Pp 289-293 (2010)
Acquired pure megakaryocytic aplasia is a rare hematological disorder characterized by thrombocytopenia with absent or markedly reduced megakaryocytes in the bone marrow. We report a case of a 25-year-old male diagnosed as acquired pure megakaryocyti
Publikováno v:
International Journal of Cardiology. 102:249-254
Data on the outcome of patients treated with thrombolytic therapy in the Arab world is scarce. The main objective of this study is to study the 7-day morbidity and mortality rate and the rate of use of thrombolytic therapy in patients presenting with
Autor:
Aisha, Al-Khinji, Michael, Linenberger
Publikováno v:
Transfusion. 55(4)
Autor:
Aisha Al-Khinji, Wing C. Chan, Alyssa Bouska, Ellen Leich, Waseem Gul Lone, Stefan Constinean, Javeed Iqbal, Tathiana Azevedo de Andrade, Andreas Rosenwald, Kai Fu
Publikováno v:
Blood. 128:5288-5288
Background: B-cell development is a complex biological process that initiates in bone marrow and matures in lymph nodes. These hierarchical stages are tightly regulated by transcription factors and microRNAs (miRNAs). B-cells are prone to genetic alt
Autor:
Aisha Al-Khinji, Elihu H. Estey, Carole Shaw, Paul C. Hendrie, Roland B. Walter, Pamela S. Becker, Kathleen Shannon Dorcy
Publikováno v:
Journal of Clinical Oncology. 34:7016-7016
7016Background: Patients with AML who, although in complete remission (CR) by conventional criteria after receipt of “intensive therapy” have measurable residual disease, (MRD) are at increased ris...