Results 111 to 120 of about 59,923 (283)
Equine Veterinary Journal, Volume 58, Issue 5, Page 1258-1268, September 2026.Abstract Background Arsenic poisoning in horses is rarely reported in the literature. However, arsenic compounds can be present in rodenticides, pesticides, and herbicides, representing a potential source of accidental exposure for horses. Objective To describe the epidemiological, clinical, and laboratory findings from a herd of 31 horses exposed to ...
Gabriella Faria Pereira +7 more
wiley +1 more source
British Journal of Clinical Pharmacology, Volume 92, Issue 8, Page 2607-2623, August 2026.Abstract The availability of safety data, particularly concerning adverse events (AEs) associated with the new shorter regimen for drug‐resistant tuberculosis (TB) containing a bedaquiline–pretomanid‐based regimen, is still limited. This systematic review aims to provide a comprehensive and updated analysis of AEs related to this new regimen by ...
Nisa Maria +4 more
wiley +1 more source
Scientific ReportsWe explore the allele and genotype distribution of UGT1A1 and BLVRA variants in individuals affected by neonatal hyperbilirubinemia in southern China.
XiuJu Liu +4 more
doaj +1 more source
Disulfiram‐Induced Hepatotoxicity in a Patient With Alcohol Use Disorder: A Case Report
Clinical Case Reports, Volume 14, Issue 8, August 2026.ABSTRACT Disulfiram can cause severe and potentially fatal hepatotoxicity, particularly in patients with preexisting liver disease. In Bhutan, where alcohol‐related liver disease represents a major public health burden and pharmacological options for relapse prevention remain limited, careful patient selection, hepatic assessment, and early monitoring ...
Sonam Wangchuk +2 more
wiley +1 more source
A Rare Diagnosis of Dubin‐Johnson Syndrome During Pregnancy: A Case Report
Clinical Case Reports, Volume 14, Issue 8, August 2026.ABSTRACT Dubin‐Johnson Syndrome (DJS) is a rare inherited disorder characterized by isolated conjugated hyperbilirubinemia without significant liver damage. This syndrome is often diagnosed incidentally during routine blood tests, as it typically presents with minimal or no symptoms.
Said Reza Modares Mousavi +5 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 8, August 2026.ABSTRACT Thrombotic thrombocytopenic purpura (TTP) is a rare, life‐threatening thrombotic microangiopathy caused by severe ADAMTS13 deficiency, usually due to autoantibody‐mediated inhibition. Its presentation is heterogeneous and often lacks the classic pentad, leading to diagnostic delays. Neurological symptoms may predominate, masking the underlying
Abdulrahman Al‐Dawoudi +4 more
wiley +1 more source
Gilbert syndrome in patients with inherited hemolytic anemia modifies the clinical phenotype
Pediatric Hematology Oncology JournalGilbert syndrome is a benign condition due to UGT1A1 mutations frequently resulting in mild, indirect hyperbilirubinemia. Inherited hemolytic anemias often present with hyperbilirubinemia and hepatosplenomegaly.
Anika Agrawal, Jagdish Chandra
doaj +1 more source
Hyperbilirubinemia and appendicular perforation peritonitis
, 2020 Rajandeep Singh Gupta +2 more
openalex +2 more sources
An effective strategy for neonatal hyperbilirubinemia [PDF]
, 2007 Alan H. Jobe
openalex +1 more source
Ecology and Evolution, Volume 16, Issue 8, August 2026.A total of 654 blood samples were collected from healthy dogs in Punjab and Khyber Pakhtunkhwa provinces in Pakistan and screened for the presence of Hepatozoon canis. Genetic diversity of the detected H. canis DNA, infection‐associated risk factors, and changes in the complete blood count of the host due to parasitic activity were also evaluated.
Madiha Rasool +14 more
wiley +1 more source