Endobronchial chondromatous hamartoma in an infant

A preterm neonate with infantile liver failure syndrome 1 due to leucyl-tRNA synthetase 1 gene (LARS1) mutations with a histopathologic phenotype of neonatal hemochromatosis.

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Chromosomal instability degrades developmental phenotypes essential for anti-GD2 immunotherapy outcomes in high-risk neuroblastoma.

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SARS-CoV-2 Placentitis: A Review of Pathologic Findings and Discussion of Differential Diagnosis.

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Real-World Medication Adherence and Medication Reviews in Adults and Children With Cystic Fibrosis.

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Less Invasive Surfactant Administration Using Video Laryngoscope to Decrease Pain in Neonates: A Randomized Controlled Trial.

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Ethical Considerations With CFTR Modulator Use in Pregnancy.

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Association Between Diaphragm Ultrasound Measures and Extubation Outcomes in Neonates: A Systematic Review and Meta-Analysis.

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Expanding the diagnostic lens: Whole exome sequencing in a neonate with arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.

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Severe Transfusion-Dependent Infantile Hemolytic Anemia Associated With a Novel Homozygous PKLR Variant of Uncertain Significance (c.1376C>G, p.Ala459Gly) and Coexisting G6PD Deficiency: A Case Report.

Cureus·2026

Stage-specific neutrophil states in neonatal injury: from antimicrobial deficiency to pro-resolution repair.

Frontiers in immunology·2026

Glycosylated Fibronectin in Fetal Growth Restriction: An Emerging Biomarker of Placental Dysfunction.

Cureus·2026

Palatoglossal Synechia in a Neonate Causing Severe Feeding Problems and Respiratory Distress: First Case Report from Somalia.

Pediatric health, medicine and therapeutics·2026

Idiopathic Epididymo-Orchitis and Pyocele in a Preterm Newborn: A Case Report.

Case reports in pediatrics·2026

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Endobronchial chondromatous hamartoma in an infant

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A preterm neonate with infantile liver failure syndrome 1 due to leucyl-tRNA synthetase 1 gene (LARS1) mutations with a histopathologic phenotype of neonatal hemochromatosis.

Beyond Pneumonia: Autoimmune Pulmonary Alveolar Proteinosis in a Pediatric Patient.

Fatal Asymptomatic Myocardial Infarction Following Stroke in a Fontan Adolescent: A Case of Occult Blastomycosis Infection.

Chromosomal instability degrades developmental phenotypes essential for anti-GD2 immunotherapy outcomes in high-risk neuroblastoma.

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Neuroblastoma, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology.

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Statewide Implementation of Stock Inhaler Programming: Respiratory Distress De-Escalation, Implementation and Utilization Experiences.

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Less Invasive Surfactant Administration Using Video Laryngoscope to Decrease Pain in Neonates: A Randomized Controlled Trial.

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Expanding the diagnostic lens: Whole exome sequencing in a neonate with arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.

Severe Transfusion-Dependent Infantile Hemolytic Anemia Associated With a Novel Homozygous PKLR Variant of Uncertain Significance (c.1376C>G, p.Ala459Gly) and Coexisting G6PD Deficiency: A Case Report.

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Endobronchial chondromatous hamartoma in an infant

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