Results 111 to 120 of about 132,601 (358)
The hyper-reactive malarial splenomegaly: a systematic review of the literature
Malaria Journal, 2015 The hyper-reactive malarial splenomegaly syndrome (HMS) is a leading cause of massive splenomegaly in malaria-endemic countries. HMS is caused by a chronic antigenic stimulation derived from the malaria parasite. Classic Fakunle’s major criteria for case
S. Leoni +4 more
semanticscholar +1 more source
Antileishmanial Activities of Carvacrol Nanoencapsulate in Biopolymeric Nanoparticles
Chemistry &Biodiversity, EarlyView.The study obtained biopolymeric nanoparticles containing carvacrol (NPCar) and evaluated their anti‐leishmanial activity. NPCar obtained presented physicochemical characteristics due to its ideal nanometric size and zeta potential, and low polydispersity index.
Joyce Cordeiro Borges +6 more
wiley +1 more source
Spontaneous rupture of the malarial spleen
The Saudi Journal of Gastroenterology, 2007 Spontaneous rupture of the spleen is a well-described occurrence in many diseases, being most commonly found in malaria. Exact incidence of this complication is not clear. In this article, we discuss pathology, diagnostic approach and therapeutic options
Tauro Leo +5 more
doaj
Spleen histology in children with sickle cell disease and hereditary spherocytosis: Hints on the disease pathophysiology [PDF]
, 2016 open2Hereditary spherocytosis (HS) and sickle cell disease (SCD) are associated with splenomegaly and spleen dysfunction in pediatric patients. Scant data exist on possible correlations between spleen morphology and function in HS and SCD.
Alaggio Rita +10 more
core +1 more source
Hereditary Elliptocytosis Resulting From Heterozygosity for β Spectrin Tandil
American Journal of Hematology, EarlyView.
María‐Angustias Molina‐Arrebola +1 more
wiley +1 more source
Chemistry &Biodiversity, EarlyView.ABSTRACT The subfamily Gomphrenoideae is composed of about 480 accepted species, many of which have been historically used as medicinal plants, reason why they have been studied in terms of chemical profile, biological activity, and safety. This review consolidates the advances in research on this subfamily over the past 47 years, emphasizing its ...
Dayanna Isabel Araque Gelves +3 more
wiley +1 more source
A Rare Case of Hemophagocytic Lymphohistiocytosis of Unknown Etiology [PDF]
, 2017 Hemophagocytic lymphohistiocytosis (HLH) is an uncommon cytokine storm syndrome marked which can cause high mortality. In adults, acquired HLH usually has an underlying infectious, autoimmune or malignant process that triggers the syndrome.
Damsker, Jason A. +3 more
core +1 more source
ChemSusChem, Accepted Article.Thalassemias are a group of inherited haemoglobinopathies that disrupt normal haemoglobin synthesis. Managing these conditions often involves regular blood transfusions and iron chelation therapy to mitigate iron overload. Among the available chelators, deferoxamine, deferasirox, and deferiprone, the latter stands out notably for its use when other ...
Francesco Basoccu +6 more
wiley +1 more source
Portal vein thrombosis : a case report and literature review [PDF]
, 2013 A case report of Portal Vein Thrombosis (PVT) as a complication of protein S deficiency. PVT has been increasingly diagnosed over the years, particularly through the use of ultrasound-Doppler equipment.
Cuschieri, Sarah +2 more
core
Autoimmune lymphoproliferative syndrome in pregnancy: a case of favorable mother - fetal outcome in a well-controlled disease [PDF]
, 2014 The autoimmune lymphoproliferative syndrome(ALPS)is a disorder of abnormal lymphocyte survival caused by the dysregulation of theFasapoptotic pathway. The Fas geneis expressed at the maternal–fetal interface and is involved in the regulation of immune ...
Baek +14 more
core +1 more source