Results 61 to 70 of about 10,393 (275)

Valproate-Induced Thrombocytopenia

open access: yesPediatric Neurology Briefs, 1994
A 14-year-old mentally retarded boy with seizures who presented with severe thrombocytopenia, macrocytic anemia and allergic dermatitis after treatment with valproate for 12 years is reported from the University of Louvain Medical School, Brussels ...
J Gordon Millichap
doaj   +1 more source

Case Report: Adenosine kinase deficiency diagnosed 10 years after liver transplantation: Novel phenotypic insights

open access: yesFrontiers in Pediatrics, 2022
Adenosine kinase (ADK) deficiency is a rare inborn error of methionine and adenosine metabolism. So far, a total of 27 patients with ADK deficiency have been reported.
Patryk Lipiński   +7 more
doaj   +1 more source

Efficacy of RBC histogram in the diagnosis of morphological types of anaemia compared with peripheral smear [PDF]

open access: yes, 2023
Background: Anaemia constitutes an important diagnostic and clinical category of haematological disorders. Along with peripheral smear histogram is used to interpret the abnormal RBC morphology.
P. L., Jayalakshmy   +2 more
core   +2 more sources

Magnitude and morphological types of anemia differ by age among under five children: A facility-based study

open access: yesHeliyon, 2022
Background: World Health Organization recently acknowledged the proportion of anemia attributable to iron deficiency among under-five children could be lower than the previously assumed 50%.
Anteneh Omer   +3 more
doaj  

Anomaly-aware multiple instance learning for rare anemia disorder classification [PDF]

open access: yesarXiv, 2022
Deep learning-based classification of rare anemia disorders is challenged by the lack of training data and instance-level annotations. Multiple Instance Learning (MIL) has shown to be an effective solution, yet it suffers from low accuracy and limited explainability.
arxiv  

Mapping VEXAS‐associated and rare UBA1 variants in the United Kingdom: Insights from patient cohorts and the general population

open access: yesBritish Journal of Haematology, EarlyView.
VEXAS syndrome is a late‐onset inflammatory disorder with rheumatological and haematological features. Epidemiological studies of VEXAS syndrome so far have been limited. Analysis of various UK cohorts estimates the incidence of VEXAS to be 1.51/100 000, or 171 new cases in the population of men over the age of 50 who are being investigated for myeloid
Ana Martinez Rodriguez   +15 more
wiley   +1 more source

Upper gastrointestinal symptoms in autoimmune gastritis. A cross-sectional study [PDF]

open access: yes, 2017
Autoimmune gastritis is often suspected for its hematologic findings, and rarely the diagnosis is made for the presence of gastrointestinal symptoms. Aims of this cross-sectional study were to assess in a large cohort of patients affected by autoimmune ...
Annibale, Bruno   +5 more
core   +2 more sources

A Novel Alternating Joint Longitudinal Model for Post-ICU Hemoglobin Prediction [PDF]

open access: yesarXiv, 2023
Anemia is common in patients post-ICU discharge. However, which patients will develop or recover from anemia remains unclear. Prediction of anemia in this population is complicated by hospital readmissions, which can have substantial impacts on hemoglobin levels due to surgery, blood transfusions, or being a proxy for severe illness.
arxiv  

Artificial intelligence supported anemia control system (AISACS) to prevent anemia in maintenance hemodialysis patients [PDF]

open access: yesarXiv, 2020
Anemia, for which erythropoiesis-stimulating agents (ESAs) and iron supplements (ISs) are used as preventive measures, presents important difficulties for hemodialysis patients. Nevertheless, the number of physicians able to manage such medications appropriately is not keeping pace with the rapid increase of hemodialysis patients.
arxiv  

A polymorphism at IGF1 locus is associated with anemia [PDF]

open access: yes, 2017
In vitro and in vivo studies suggest that IGF-1 has a role in erythropoiesis. There is evidence that the rs35767 C/T polymorphism near IGF1 is associated with plasma IGF-1 levels.
Andreozzi F   +5 more
core   +1 more source

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