Results 51 to 60 of about 6,512 (195)
Journal of Child Psychology and Psychiatry, EarlyView.Background Attention‐deficit/hyperactivity disorder (ADHD) is a chronic neurodevelopmental disorder marked by persistent patterns of inattention, disorganization, hyperactivity, and impulsivity. Increasing evidence implicates immune‐inflammatory processes in its etiology, with observed associations between ADHD and infectious diseases, allergic ...
Eugene Merzon +11 more
wiley +1 more source
Racemisation of Amino Acids: From Synthetic Challenge to Biological Significance
ChemBioChem, Volume 27, Issue 11, 15 June 2026.Racemisation, once considered an undesirable synthetic side reaction, also occurs naturally in amino acids and influences biological processes. Evidence links stereochemical conversion to ageing, protein turnover, and cellular development. This review examines mechanisms, control strategies in synthesis, applications and implications in physiology ...
Othman Al Musaimi
wiley +1 more source
Histopathology of Hereditary Spherocytosis
, 2022 This presentation will reveal the the histological effects of Hereditary Spherocytosis through the use of histologic photomicrographs and research on the inherited blood ...
Suh, Eric
core
Intrathoracic Extramedullary Hematopoiesis Arising in the Anterior Mediastinum
Clinical Case Reports, Volume 14, Issue 6, June 2026.Arrows indicate enlarging anterior (a, b) and posterior (c, d) mediastinal extramedullary hematopoiesis (EMH). EMH should be included in the differential diagnosis of anterior mediastinal lesion. Histologic confirmation is desirable to obtain definitive diagnosis and guide management.
Yoshiki Kozu +3 more
wiley +1 more source
Spherocytosis in Newborn Secondary to Novel Heterozygous Mutation in Gene: Case Report
Journal of Investigative Medicine High Impact Case Reports, 2023 This case report describes a novel mutation of the SPTB gene as a potential pathogenic cause of spherocytosis. A 3-week-old male presented with clinical and laboratory signs consistent with hemolytic spherocytosis, including jaundice, hyperbilirubinemia,
Daphna Varadi MD +3 more
doaj +1 more source
Hereditary Spherocytosis and Wandering Spleen
Pediatric Hematology and Oncology, 2013 Pelvic spleen is a very rare condition especially among children [1]. There were 130 pediatric cases reported in the literature [2].
Özgürler, Funda +4 more
openaire +6 more sources
Food Chemistry International, Volume 2, Issue 2, Page 246-262, June 2026.After collecting Musa paradisiaca leaves, some were dried and others were used to produce aqueous extracts. The extracts and powders were characterized and then administered to rats made anaemic by PHZ. After 14 days of administration of the two samples, the rats were euthanized and it was observed that after 9 days of treatment, the aqueous extract ...
Josée Rebeca Nombo +8 more
wiley +1 more source
Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis
Frontiers in Pediatrics, 2019 A 3-year-old girl was admitted to our hospital for the correction of atrial septal defect (ASD). Open heart operation with cardiopulmonary bypass is dangerous because the patient also had hereditary spherocytosis, which put her at risk for hemolytic ...
Zhixian Ji +6 more
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The Pan African Medical Journal, 2019 Hereditary spherocytosis is a rare cause of chronic haemolytic anaemia. It is rarer in the black population with extremely few cases reported. Initial assessment of a patient with suspected disease should include documenting clinical features of chronic ...
Khaled Elmezughi, Chukwuma Ekpebegh
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Hereditary spherocytosis with immunoglobulin A nephropathy
, 2010 Hereditary spherocytosis is a familial hemolytic anemia. Immunoglobulin A (IgA) nephropathy associated with hereditary spherocytosis has not been reported in children.
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