Results 121 to 130 of about 345,333 (344)

The Application of Artificial Intelligence‐Based Bone Marrow Cell Analysis System in Pediatric Hematological Diseases

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Introduction The clinical diagnosis of hematological diseases depends on the differential count of nucleated cells on the bone marrow (BM) smears, and an artificial intelligence (AI)‐based system was applied to automatically classify BM nucleated cells in pediatric hematological disease samples in this study.
Xin He, Fei He, Yan Wang, Yu Liu, Xiaopeng Gao, Mingrui Yu, Haiyan Gao   +6 more
wiley   +1 more source

How Classmates Experience Visiting Their Hospitalised Peer During Cancer Treatment: A RESPECT Study

Journal of Advanced Nursing, EarlyView.
ABSTRACT Aim To explore how classmate ‘ambassadors’ experienced and engaged in social interaction while visiting a hospitalised peer undergoing cancer treatment. Design A phenomenological‐hermeneutic inspired exploratory study. Methods Using on‐the‐go semi‐structured interviews and participant observations from January to December 2023 in Denmark, we ...
Natasha Nybro Boensvang, Martin Kaj Fridh, Claire Elizabeth Wakefield, Pernille Envold Bidstrup, Hanne Bækgaard Larsen   +4 more
wiley   +1 more source

Exome sequencing identifies MPL as a causative gene in familial aplastic anemia

Haematologica, 2012
The primary cause of aplastic anemia remains unknown in many patients. The aim of this study was to clarify the genetic cause of familial aplastic anemia.
Amanda J. Walne, Arran Dokal, Vincent Plagnol, Richard Beswick, Michael Kirwan, Josu de la Fuente, Tom Vulliamy, Inderjeet Dokal   +7 more
doaj   +1 more source

Feminization and severe pancytopenia caused by testicular neoplasia in a cryptorchid dog [PDF]

, 2016
In this case report, a paraneoplastic syndrome caused by testicular neoplasia in a ten-year-old cryptorchid dog is described. Feminization and pancytopenia were observed, resulting from the testicular neoplastic production of estrogens.
Hebbelinck, Lien, Kitshoff, Adriaan, Paepe, Dominique, Vandenabeele, Sophie   +3 more
core  

Concurrent treatment of aplastic anemia/paroxysmal nocturnal hemoglobinuria syndrome with immunosuppressive therapy and eculizumab: a UK experience

Haematologica, 2018
Paroxysmal nocturnal hemoglobinuria (PNH), an ultraorphan disease with a prevalence of 15.9 per million in Europe, is a life threatening disorder characterized by hemolysis, bone marrow failure and thrombosis.
M. Griffin, A. Kulasekararaj, Sheyans Gandhi, T. Munir, S. Richards, L. Arnold, Nana Benson-Quarm, N. Copeland, Isabel Duggins, Kathryn Riley, P. Hillmen, J. Marsh, A. Hill   +12 more
semanticscholar   +1 more source

Challenges of Parents While Providing Complex Medical Care at Home to Children With Cancer: A Cross‐Sectional Convergent Mixed Methods Study

Journal of Clinical Nursing, EarlyView.
ABSTRACT Aim To explore challenges parents of children with cancer encounter while providing complex medical care at home. Methods Design: Cross‐sectional convergent mixed‐methods study. Instruments: Questionnaire and open interviews that mirrored and complemented each other.
Rachel Klausner Shyman, Sveta Roberman, Gal Goldstein, Sabaa Masarwe, Amy Solnica, Rachel Yaffa Zisk‐Rony   +5 more
wiley   +1 more source

Early evidence of bone marrow dysfunction in children with indeterminate fulminant hepatic failure who ultimately develop aplastic anemia. [PDF]

, 2004
In children, aplastic anemia (AA) is a common complication associated with fulminant hepatic failure (FHF). The objective of this study was to determine whether specific pretransplantation clinical and laboratory characteristics can be used to ...
Ingram-Drake, Leslie, Katzir, Lirona, Krogstad, Paul, Martín, Martín G, Molina, Ricardo A, Moore, Ted, Rhee, Chris   +6 more
core  

Patient‐Reported Oral Symptoms and Their Impact on Well‐Being After Haematopoietic Cell Transplantation

Oral Diseases, EarlyView.
ABSTRACT Objective Oral complications may negatively influence outcomes of haematopoietic cell transplantation (HCT). A comprehensive view of oral symptoms and symptom burden post‐HCT is lacking. This study aimed to determine the prevalence, severity, and temporal relationships of oral symptoms and their impact on well‐being in the early post‐HCT phase.
Kristina Skallsjö, Michael T. Brennan, Bengt Hasséus, Jenny Öhman, Judith E. Raber‐Durlacher, Marie‐Charlotte D. N. J. M. Huysmans, Alexa M. G. A. Laheij, Stephanie J. M. van Leeuwen, Allan J. Hovan, Karin Garming Legert, Scott Isom, David M. Kline, Nicole M. A. Blijlevens, Jan‐Erik Johansson, Inger von Bültzingslöwen   +14 more
wiley   +1 more source

Aplastic anemia associated with interferon alpha 2a in a patient with chronic hepatitis C virus infection: a case report

Journal of Medical Case Reports, 2010
Introduction Hepatitis-associated aplastic anemia is a common syndrome in patients with bone marrow failure. However, hepatitis-associated aplastic anemia is an immune-mediated disease that does not appear to be caused by any of the known hepatitis ...
Ioannou Savvas, Hatzis Gregorios, Vlahadami Ioanna, Voulgarelis Michael   +3 more
doaj   +1 more source

Consensus of German Transplant Centers on Hematopoietic Stem Cell Transplantation in Fanconi Anemia [PDF]

, 2015
Allogeneic hematopoietic stem cell transplantation (HSCT) is currently the only curative therapy for the severe hematopoietic complications associated with Fanconi anemia (FA). In Germany, it is estimated that 10–15 transplants are performed annually for
Bader, P., Beier, R., Burkhardt, B., Chao, M. M., Ebell, W., Feuchtinger, T., Handgretinger, R., Hanenberg, H., Koehl, U., Kratz, C., Kremens, B., Lang, P., Meisel, R., Mueller, I., Roessig, C., Sauer, M., Schlegel, P. G., Schulz, A., Strahm, B., Sykora, K. W., Thol, F.   +20 more
core   +1 more source