Results 241 to 250 of about 102,449 (341)
Hypertension, proteinuria, and RAAS inhibition use in children with systemic lupus erythematosus: Data from a multi-institutional pediatric learning health system. [PDF]
Chang JC+17 more
europepmc +1 more source
Steroid‐responsive generalised sterile necrotising pyogranulomatous lymphadenitis in a cat
A 1.5‐year‐old neutered male cat was presented with fever, inappetence, lethargy and marked generalised lymphadenopathy of 4 days duration. Excisional biopsy of peripheral lymph nodes revealed necrotising pyogranulomatous lymphadenitis. Extensive investigation failed to identify an underlying infectious [bacterial (Bartonella, Mycobacteria, Mycoplasma,
L. Lecot+4 more
wiley +1 more source
Features of Undiagnosed Abdominal Pain and Diagnostic Status of Acute Hepatic Porphyria in Japan: A Retrospective Study. [PDF]
Tago M+15 more
europepmc +1 more source
Objective The objective of the study was to determine the biological variation of select serum biochemistry analytes and fibroblast growth factor 23 in both clinically healthy cats and cats with chronic kidney disease. Methods Eleven healthy cats and seven cats with chronic kidney disease International Renal Interest Society Stages 2 and 3 were ...
S. Summers+3 more
wiley +1 more source
Investigations for diagnosis of secondary hypertension in children: yield and costs. [PDF]
Guarino S+8 more
europepmc +1 more source
ABSTRACT Background Alopecia areata (AA) is an autoimmune disease characterized by hair loss that can negatively impact quality of life. AA has a significant pediatric prevalence; however, no systemic treatments are approved for AA in patients aged < 12 years. Ritlecitinib, a JAK3/TEC family kinase inhibitor, is approved to treat adults and adolescents
Mercedes E. Gonzalez+7 more
wiley +1 more source
Performance verification of the new UF-1500 urine particle analyser: a new opportunity for small and medium laboratories. [PDF]
Previtali G+14 more
europepmc +1 more source
ABSTRACT Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by progressive heterotopic ossification (HO) and congenital malformation of the great toes. This case describes a 5‐year‐old Caucasian girl who initially presented with painless neck and back swelling as well as severe limitation of movement in the neck and ...
Orhan Yilmaz, Loretta Fiorillo
wiley +1 more source
A Systematic Review of the Accuracy and Reliability of Pyuria in Diagnosing Pediatric Urinary Tract Infections. [PDF]
Sameer SK+9 more
europepmc +1 more source