Zobrazeno 1 - 10
of 21
pro vyhledávání: '"A K Mallhi"'
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100835- (2023)
Externí odkaz:
https://doaj.org/article/d032a9492f914d1281cdcae3c0844a0d
Autor:
Leon Chen, Shahidul Islam, David Buchbinder, Ashley V Geerlinks, Hannah L Elfassy, Christiane Querfeld, Jeffrey I. Cohen, Blachy J. Dávila Saldaña, Deborah Schiff, Helen E. Heslop, William Owen, Weni Chang, Martha Pacheco, Evan Shereck, Michael B. Jordan, Nameeta Richard, Catherine M. Bollard, David Hagin, Niraj C. Patel, Shanmuganathan Chandrakasan, Tami D John, Sharat Chandra, Holly K. Miller, Rakesh K. Goyal, Roger Giller, Troy C. Quigg, Elizabeth Stenger, Kanwaldeep K. Mallhi, Challice L. Bonifant
Publikováno v:
Blood Advances
Blood advances, vol 6, iss 2
Blood advances, vol 6, iss 2
Key Points Stem cell transplant improves long-term survival in T/NK CAEBV, though mortality remains high.Development of T/NK lymphoma showed a trend with increased mortality.
Visual Abstract
Chronic active Epstein-Barr virus (EBV) disease (
Visual Abstract
Chronic active Epstein-Barr virus (EBV) disease (
BK viremia and changes in eGFR in children and young adults after hematopoietic cell transplantation
Autor:
Chiara, Wychera, Hannah N, Imlay, Elizabeth R, Duke, Anna, Faino, Meei, Li-Huang, Terry, Stevens-Ayers, Chris, Davis, Baerbel, Lange-Sperandio, Kanwaldeep K, Mallhi, Joshua A, Hill, Michael, Boeckh, Janet A, Englund, Sangeeta, Hingorani
Publikováno v:
Transplantation and cellular therapy.
Kidney disease in allogeneic hematopoietic cell transplant (HCT) recipients is associated with increased mortality rates. BK virus (BKV) viremia has been associated with kidney dysfunction in pediatric HCT recipients, however, few studies have invest
Publikováno v:
Journal of Blood Medicine
The Wiskott–Aldrich syndrome (WAS) is an X-linked disorder caused by mutations in the WAS gene resulting in congenital thrombocytopenia, eczema, recurrent infections and an increased incidence of autoimmune diseases and malignancies. Without curati
Autor:
Alpana Waghmare, Masumi Ueda Oshima, Hu Xie, Kanwaldeep K. Mallhi, Chikara Ogimi, Michael Boeckh, Keith R. Jerome, Wendy M. Leisenring, Janet A. Englund
Publikováno v:
Blood Advances
Data are limited regarding risk factors for lower respiratory tract infection (LRTI) caused by seasonal human coronaviruses (HCoVs) and the significance of virologic documentation by bronchoalveolar lavage (BAL) on outcomes in hematopoietic cell tran
Autor:
Monica S. Thakar, Suzanne Skoda-Smith, Brenda M. Sandmaier, Ann E. Woolfrey, Hans-Peter Kiem, Haydar Frangoul, Aleksandra Petrovic, Kanwaldeep K. Mallhi, Lauri Burroughs, Meera A. Srikanthan, Kelsey Baker, Paul A. Carpenter, Troy R. Torgerson, Amy E. Geddis, K. Scott Baker, Rainer Storb
Publikováno v:
Biol Blood Marrow Transplant
Allogeneic hematopoietic cell transplant (HCT) is often the only curative therapy for patients with nonmalignant diseases; however, many patients do not have an HLA-matched donor. Historically, poor survival has been seen after HLA-haploidentical HCT
Autor:
Chiara Wychera, Hannah N. Imlay, Elizabeth R. Duke, Anna Faino, Meei Li-Huang, Terry Stevens-Ayers, Chris Davis, Baerbel Lange-Sperandio, Kanwaldeep K. Mallhi, Joshua A. Hill, Michael Boeckh, Janet A. Englund, Sangeeta Hingorani
Publikováno v:
Transplantation and Cellular Therapy. 29:187.e1-187.e8
Autor:
Hemalatha G. Rangarajan, Joseph R. Stanek, Hisham Abdel-Azim, Arunkumar Modi, Ann Haight, Christopher M. McKinney, Daniel J. McKeone, David K. Buchbinder, Emmanuel Katsanis, Ghada A. Abusin, Ibrahim Ahmed, Jason Law, Jorge Galvez Silva, Kanwaldeep K. Mallhi, Lauri M. Burroughs, Niketa Shah, Peter J. Shaw, Robert Greiner, Shalini Shenoy, Michael A. Pulsipher, Rolla Abu-Arja
Publikováno v:
Transplantation and Cellular Therapy. 28:329.e1-329.e9
Hematopoietic cell transplantation (HCT) is the sole curative option for congenital dyserythropoietic anemia (CDA), a rare type of hemolytic anemia characterized by anemia, ineffective erythropoiesis, and secondary hemochromatosis. In this retrospect
Autor:
Emmanuel Katsanis, Arunkumar Modi, Hemalatha G. Rangarajan, Kanwaldeep K. Mallhi, Ibrahim Ahmed, Joseph Stanek, Daniel J. McKeone, Ghada Abusin, Robert J. Greiner, Ann E. Haight, Shalini Shenoy, Lauri S Burroughs, Jorge Galvez Silva, David Buchbinder, Jason Law, Rolla Abu-Arja, Peter J. Shaw, Christopher M. McKinney, Michael A. Pulsipher, Hisham Abdel-Azim
Publikováno v:
Blood. 136:42-43
Introduction Congenital dyserythropoietic anemias (CDA) are a rare group of hereditary disorders characterized by anemia, ineffective erythropoiesis, and secondary hemochromatosis. While some CDA patients respond to interferon α therapy (type I CDA)
Autor:
Chikara Ogimi, Hu Xie, Alpana Waghmare, Masumi Ueda, Kanwaldeep K Mallhi, Chris Davis, Ashley Akramoff, Anthony Mallory, Keith R Jerome, Wendy M Leisenring, Janet A Englund, Michael Boeckh
Publikováno v:
Open Forum Infectious Diseases
Background Proven/probable lower respiratory tract infection (LRTI) caused by seasonal human coronaviruses (HCoVs) is associated with mortality after hematopoietic cell transplantation (HCT). However, risk factors for LRTI and the significance of vir