Results 101 to 110 of about 17,995 (265)

A case of LGL leukemia with paucity of erythropoiesis

open access: yesClinical Case Reports, 2020
The differential diagnosis for neutropenia is large and includes, drug effect, viral infections, sepsis, immune, hypersplenism, and bone marrow disorder. The presence of an autoimmune disorder and large granular lymphocytosis should prompt assessment for
Habib M. Razavi
doaj   +1 more source

Pure Red Cell Aplasia After Kidney Transplantation: Parvovirus B19 Culprit or Coincidence?

open access: yesAnnals of Transplantation, 2019
Background Anemia is present even in long-term observation after kidney transplantation. Observational study results indicate the presence of chronic post-transplantation anemia in 1 in 3 recipients.
K. Pabisiak   +2 more
semanticscholar   +1 more source

A Case of Atrial Fibrillation from Cyclosporine Toxicity [PDF]

open access: yes, 2004
We describe the unusual occurrence of atrial fibrillation immediately after a seizure in a young patient with cyclosporine toxicity. The new onset atrial fibrillation was triggered by high levels of cyclosporine and possibly facilitated by the ...
Ahmad, Masood, Sanghi, Pramod
core   +2 more sources

Infectious Diseases Associated With Renal Homotransplantation: I. Incidence, Types, and Predisposing Factors [PDF]

open access: yes, 1964
Infectious diseases occurred in 26 of 30 renal homotransplantation patients and contributed to eight of the 12 deaths in this series. There were 52 infections, 17 occurring before and 35 after transplantation.
Marchioro, TL   +3 more
core   +1 more source

A Rare Giant Pleural Thymoma in Posterior Mediastinum. [PDF]

open access: yes, 2012
Thymoma is an epithelial neoplasm of the thymus, which commonly lies in the anterior mediastinum. Unusually, thymomas can also be found in other locations. Surgical excision, when feasible, appears to provide good results. We encountered a rare case of a
Kalloli, M   +3 more
core  

Pure Red Cell Aplasia (PRCA) and Cerebellar Hypoplasia as Atypical Features of Polyglandular Autoimmune Syndrome Type I (APS-1): Two Sisters With the Same AIRE Mutation but Different Phenotypes

open access: yesFrontiers in Pediatrics, 2019
The polyglandular autoimmune syndrome type I is a rare hereditary autosomal recessive disease. We describe a child with the classic triad of the disease and her sister with pure red cell aplasia and cerebellar hypoplasia.
Matteo Chinello   +10 more
doaj   +1 more source

Infrequent Replication of Parvovirus B19 and Erythrovirus Genotypes 2 and 3 among HIV-Infected Patients with Chronic Anemia [PDF]

open access: yes, 2017
We investigated the role that erythroviruses (parvovirus B19 and erythrovirus genotypes 2 and 3) play in the lives of immunosuppressed HIV-infected patients with chronic anemia.
Bernasconi, Enos   +10 more
core  

Canine autoimmune hemolytic anemia: management challenges. [PDF]

open access: yes, 2016
Immune-mediated hemolytic anemia is one of the most common manifestations of canine immune-mediated disease, yet treatment regimens remain nonstandardized and, in some cases, controversial.
Skelly, Barbara J, Swann, James W
core   +2 more sources

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