Detect early, protect kidney health: World Kidney Day 2025
Pediatr Nephrol. 2025 Feb 17. doi: 10.1007/s00467-025-06714-4. Online ahead of print. NO ABSTRACT PMID:39960639 | DOI:10.1007/s00467-025-06714-4
paediatrics
The Bidirectional Relationship Between Iron Deficiency Anemia and Chronic Headache Disorders: A Systematic Review and Meta-Analysis
Anemia. 2025 Feb 7;2025:5695022. doi: 10.1155/anem/5695022. eCollection 2025. ABSTRACT Background and Objective: IDA and chronic headache disorders such as migraines and tension-type headaches are common …
An Alarm for Pediatricians Facing BCG Vaccine Complications
Tanaffos. 2024 Feb;23(2):100-101. NO ABSTRACT PMID:39959804 | PMC:PMC11825073
Is Non-Invasive Ventilation a Good Choice in All Patients with Severe COVID-19? A Cohort Retrospective Study
Tanaffos. 2024 Feb;23(2):176-182. ABSTRACT BACKGROUND: The recent outbreak of Coronavirus 2019 (COVID-19) is a respiratory disorder caused by the Acute Respiratory Syndrome Coronavirus 2. At …
Granulocyte colony-stimulating factor reduces biliary fibrosis and ductular reaction in a mouse model of chronic cholestasis
Liver Res. 2023 Mar 6;7(1):90-98. doi: 10.1016/j.livres.2023.02.004. eCollection 2023 Mar. ABSTRACT BACKGROUND: Biliary atresia is a rare congenital bile duct disease that is the leading …
Mycoplasma pneumoniae pneumonia in children
World J Clin Cases. 2025 Feb 16;13(5):99149. doi: 10.12998/wjcc.v13.i5.99149. ABSTRACT Mycoplasma pneumoniae (M. pneumoniae) is a common pathogen that causes community-acquired pneumonia in children. The …
Case Report – Severe hypospadias in 46, XY karyotype patients: is third level genetic testing always mandatory?
Front Surg. 2025 Jan 31;12:1524953. doi: 10.3389/fsurg.2025.1524953. eCollection 2025. ABSTRACT We report a case of a 4-month-old infant with severe genital malformation and a 46, …
Novel Intronic Heterozygous Mutation in TSC2 Gene in Pediatric Patient with Tuberous Sclerosis Complex
Acta Inform Med. 2024;32(2):122-125. doi: 10.5455/aim.2024.32.122-125. ABSTRACT BACKGROUND: Tuberous Sclerosis Complex (TSC) is an autosomal dominant genetic disorder and involves multiple organs, intellectual disability and …
Left Portal Hypertension and Hypersplenism in a Child With Congenital Diaphragmatic Hernia: A Rare Case Report
Acta Inform Med. 2024;32(2):135-138. doi: 10.5455/aim.2024.32.135-138. ABSTRACT BACKGROUND: T Congenital diaphragmatic hernia (Bochdalek hernia), which occurs in 1/2,200 live births, is typically diagnosed in the …
Robot-assisted percutaneous cannulated screw fixation in the treatment of slipped capital femoral epiphysis
J Child Orthop. 2025 Feb 14:18632521251319987. doi: 10.1177/18632521251319987. Online ahead of print. ABSTRACT PURPOSE: To investigate robot-assisted percutaneous cannulated screw fixation for treating slipped capital …