Results 81 to 90 of about 339,316 (310)

Bilateral Spontaneous Hyphemas in a Patient with Aplastic Anemia

Case Reports in Ophthalmology, 2018
Bilateral spontaneous hyphemas are a rare ophthalmic event. Aplastic anemia is a hematologic condition with well-documented manifestations in the posterior segment but not the anterior segment.
Mohammad Z. Siddiqui, Grant Gebhard, Alice Behrens, Ahmed Sallam, Sami Uwaydat   +4 more
doaj   +1 more source

Case Report: Hematopoietic Stem Cell Transplantation to Treat Severe Acquired Aplastic Anemia in a Pediatric Kidney Transplant Recipient [PDF]

Pediatr Transplant
ABSTRACT Background Hematopoietic stem cell transplantation (HSCT) in solid organ transplant recipients has been reported in adults. However, data on children are scarce. We report a case of an allogeneic HSCT in a 14‐year‐old girl to treat idiopathic very severe aplastic anemia (SAA). Case Presentation The girl developed end‐stage renal disease at the
Mierkienė G, Vaitkevičienė G, Ažukaitis K, Jankauskienė A, Rascon J.   +4 more
europepmc   +2 more sources

Idiopathic aplastic anemia vs hypocellular myelodysplastic syndrome.

Hematology. American Society of Hematology. Education Program, 2019
Proper diagnostic distinction of bone marrow failure syndromes can often be challenging. In particular, for older patients with idiopathic aplastic anemia (AA), differential diagnosis includes myelodysplastic syndrome (MDS), which can atypically present ...
J. Durrani, J. Maciejewski
semanticscholar   +1 more source

Diagnosis and Management of Hypersensitivity to Antiplatelet Drugs: EAACI Position Paper

Allergy, EarlyView.
ABSTRACT Antiplatelet drug (APD) therapy is the cornerstone for the prevention of atherosclerotic cardiovascular disease. The main APDs are aspirin and thienopyridines, particularly clopidogrel. These drugs may induce hypersensitivity reactions (HSRs).
Gabriele Cortellini, Alla Nakonechna, Annick Barbaud, Sevim Bavbek, Gianfranco Calogiuri, Inmaculada Doña, Violeta Kvedariene, Jose Julio Laguna Martinez, Serena Liberati, Mauro Pagani, Antonino Romano   +10 more
wiley   +1 more source

Показатели обмена глюкозы в эритроцитах при отдельных гематологических заболеваниях [PDF]

, 2013
Установлено, що за еритремії, апластичній анемії та залізодефіцитній анемії в еритроцитах відбувається інтенсифікація гліколітичних реакцій, про що свідчить підвищення активності гексокінази і вмісту метаболіту гліколізу – фосфоенолпірувату, а також ...
Казакова, В.В., Коношенко, С.В., Ёлкина, Н.М.   +2 more
core  

Altered expression of the TCR signaling related genes CD3 and FcεRIγ in patients with aplastic anemia [PDF]

, 2012
Background Aplastic anemia (AA) is characterized by pancytopenia and bone marrow hypoplasia, which results from immune-mediated hematopoiesis suppression.
AM Wegener, B Malissen, Bo Li, C Dufour, E Sloand, ED Zanders, EE Solomou, EJ Enyedy, EN Kersh, F Zhou, H Clevers, H Murata, JM Oliver, JP Maciejewski, K Amemiya, K Kaito, KJ Livak, L Ciszak, L Shiue, LA Pitcher, Lijian Yang, ME Call, ME Call, N Taylor, NC Zoumbos, NC Zoumbos, NS Young, NS Young, S Chen, S Koyasu, S Krishnan, SD Thompson, Shaohua Chen, Sichu Liu, Su Fang, T Kato, Xiuli Wu, Y Li, Yangqiu Li, Yuzhe Niu, Zhi Yu, ZM Sun   +41 more
core   +2 more sources

Pathogenesis of Acquired Aplastic Anemia and the Role of the Bone Marrow Microenvironment

Frontiers in Oncology, 2018
Aplastic anemia (AA) is characterized by bone marrow (BM) hypocellularity, resulting in peripheral cytopenias. An antigen-driven and likely auto-immune dysregulated T-cell homeostasis results in hematopoietic stem cell injury, which ultimately leads to ...
M. Medinger, B. Drexler, C. Lengerke, J. Passweg   +3 more
semanticscholar   +1 more source

Battle in the Clouds

American Anthropologist, EarlyView.
ABSTRACT This narrative experiment brings together scenes from my family histories in western Pennsylvania coal country, alongside ongoing visits to learn about rising health issues in the region today. Increasing numbers of residents express concerns about chronic problems such as young cancers, and many people worry about potential exposures coming ...
Amy Moran‐Thomas
wiley   +1 more source

Response of Paroxysmal Nocturnal Hemoglobinuria Clone with Aplastic Anemia to Rituximab

Case Reports in Hematology, 2012
Paroxysmal nocturnal hemoglobinuria is caused by expansion of a hematopoietic stem cell clone with an acquired somatic mutation in the PIG-A gene. This mutation aborts the synthesis and expression of the glycosylphosphatidylinositol anchor proteins CD55
Radha Raghupathy, Olga Derman
doaj   +1 more source

Barnes Hospital Bulletin [PDF]

, 1975
https://digitalcommons.wustl.edu/bjc_barnes_bulletin/1120/thumbnail ...

core   +1 more source