Results 171 to 180 of about 37,879 (224)
Pediatric Systemic Lupus Erythematosus Complicated by Acute EBV and CMV Co-infection. [PDF]
J Clin Lab AnalChen A +7 more
europepmc +1 more source
Repurposing Gaucher disease therapy for Saposin C deficiency: Proof-of-concept with eliglustat.
Mol Genet MetabMinea C, Deegan PB.
europepmc +1 more source
Mastocytosis Manifested by Hepatosplenomegaly
New England Journal of Medicine, 1964 CURRENT interest in the function and pathophysiology of the mast cell has been exemplified by a recent symposium on the subject.1 However, arguments over the derivation of the mast cell and its function and role in diseases remain unresolved. Pathologic states involving the mast cell can take several forms, which have been arbitrarily divided into ...
J S, GONNELLA, A I, LIPSEY
openaire +3 more sources
Chronic Hepatosplenomegaly in African School Children: A Common but Neglected Morbidity Associated with Schistosomiasis and Malaria [PDF]
PLoS Neglected Tropical Diseases, 2011 Chronic hepatosplenomegaly, which is known to have a complex aetiology, is common amongst children who reside in rural areas of sub-Saharan Africa.
Birgitte J Vennervald +2 more
exaly +4 more sources
Health implications of chronic hepatosplenomegaly in Kenyan school-aged children chronically exposed to malarial infections and Schistosoma mansoni. [PDF]
Transactions of the Royal Society of Tropical Medicine and Hygiene, 2010 Hepatosplenomegaly among school-aged children in sub-Saharan Africa is highly prevalent. Two of the more common aetiological agents of hepatosplenomegaly, namely chronic exposure to malaria and Schistosoma mansoni infection, can result in similar ...
Birgitte J Vennervald +2 more
exaly +2 more sources
Hepatosplenomegaly, pancytopenia, and fever
The Journal of Pediatrics, 1973 Jay Bernstein +2 more
openaire +3 more sources