Results 51 to 60 of about 60,277 (228)
Nephrotic Syndrome Associated with Thymoma
Thymoma is associated with a wide variety of paraneoplastic syndromes such as myasthenia gravis, pure red cell aplasia, and hypogammaglobulinemia. Paraneoplastic glomerulonephritis is a rare clinical presentation of malignancy.
Sheng-Yen Hsiao +3 more
doaj +1 more source
The definition of nephrotic syndrome is proteinuria accompanied by hypoalbuminaemia and oedema. This, however, is not a direct chain of events. In the presence of normal liver albumin synthesis, nephrotic range of proteinuria (> 3.5 g/24 h) should not cause hypoalbuminaemia, and a low plasma albumin concentration itself does not result in oedema ...
openaire +2 more sources
Nephrotic syndrome secondary tocytomegalovirus infection inan infant. Case report
Introduction: Nephrotic syndrome in children is usually idiopathic and the first episode is rarely observed before the 1st year of life. Viral infections are a rare cause of this condition.
Małgorzata Stańczyk, Marcin Tkaczyk
doaj +1 more source
Objectives The study aimed (a) to establish the reference interval for Δmean corpuscular haemoglobin concentration‐mean cellular haemoglobin concentration in healthy dogs by ADVIA 2120 haematology analyser, (b) to identify the causes of increased Δmean corpuscular haemoglobin concentration‐mean cellular haemoglobin concentration in both healthy and ...
M. G. Ferrari +5 more
wiley +1 more source
ABSTRACT Children undergoing allogeneic stem cell transplantation often receive off‐label rituximab treatment for Epstein–Barr virus reactivation, using adult dosing without pediatric evidence. This project aims to develop a clinical decision support tool (CDSS) that provides evidence‐based dosing scenarios by analyzing real‐world patient data.
Birgit Burkhardt +2 more
wiley +1 more source
Advanced Paternal Age Impacts Common Loci in the Sperm and Placenta DNA Methylomes
ABSTRACT Background Epidemiological studies have reported an association between advanced paternal age at conception and an increased risk of neurodevelopmental disorders in offspring, such as autism spectrum disorder. Evidence suggests that DNA methylation alterations in spermatozoa of older men may be transmitted to the feto‐placental unit and ...
Julia Barnwell +12 more
wiley +1 more source
ABSTRACT Background and Aims Epidermolysis bullosa is a rare genetic disorder causing extreme mucocutaneous fragility, requiring specialized, multidisciplinary care. Integrating palliative care into Epidermolysis bullosa management has proven beneficial in symptom control and psychosocial support.
Juan Manuel Martínez‐Ripoll +2 more
wiley +1 more source
Idiopathic nephrotic syndrome (INS) is the most common and challenging glomerular disease in childhood and most children respond favorably to glucocorticoid therapy.
Wen-jing Kang +2 more
doaj +1 more source
Abstract Cryoglobulinemia (CG) is defined by the presence of serum immunoglobulins that precipitate below 37°C and redissolve upon rewarming. It is classified into three types based on immunoglobulin composition. Type I, a rare form, involves monoclonal IgM or IgG and is linked to lymphoproliferative disorders.
Anna Linda Zignego +7 more
wiley +1 more source
Ischemic Stroke in Hypereosinophilic Syndrome: A Clinicopathologic Study of Two Cases
ABSTRACT Ischemic stroke is a rare complication of hypereosinophilic syndrome (HES). Manifestations of stroke in HES have been described in the radiologic literature; however the pathologic characterization of central nervous system (CNS) involvement in HES is limited.
Karina C. Martin +3 more
wiley +1 more source

