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Pediatric Reports|August 26, 2026
The Diagnostic Journey from Rhabdomyolysis to Myopathy with Tubular Aggregates: A Family-Based Case Report and Review of the LiteratureSlavica Ostojić, Sanja Milenković, Sonja Pavlović, et al.
Pediatric Reports|July 20, 2016
Novel Use of an Ultrafiltration Device as an Alternative Method for Fluid Removal in Critically Ill Pediatric Patients with Cardiac Disease: A Case SeriesSujata Chakravarti, Yasir Al-Qaqaa, Meghan Faulkner, et al.
Pediatric Reports|April 29, 2015
Malignant rhabdoid tumor of the liver: a case report and literature reviewSatoru Oita, Keita Terui, Syugo Komatsu, et al.
Pediatric Reports|April 29, 2015
Determinants of stillbirths in katsina, Nigeria: a hospital-based studyBello M Suleiman, H M Ibrahim, N Abdulkarim
Pediatric Reports|April 29, 2015
Acute respiratory distress syndrome associated with tumor lysis syndrome in a child with acute lymphoblastic leukemiaAlessandra Macaluso, Selene Genova, Silvio Maringhini, et al.
Pediatric Reports|April 30, 2021
Exstrophy-Epispadias Complex Variants: A Hybrid CaseAlba Ganarin, Michele Corroppolo, Giosuè Mazzero, et al.
Pediatric Reports|October 31, 2017
Atypical clinical presentation and successful treatment with oral cholic acid of a child with defective bile acid synthesis due to a novel mutation in the HSD3B7 geneGrazia Bossi, Giuseppe Giordano, Gaetana Anna Rispoli, et al.
Pediatric Reports|October 31, 2017
Free-Aspire: A new device for the management of airways clearance in patient with ineffective coughLuca Bertelli, Giovanni Di Nardo, Salvatore Cazzato, et al.
Pediatric Reports|October 31, 2017
Congenital vitiligo: A case observed in the cohort of HIV-exposed infants in Bobo-Dioulasso, Burkina FasoMakoura Barro, Jean W Diallo, Ad Bafa Ibrahim Ouattara, et al.
Pediatric Reports|October 31, 2017
Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousinsCristina Olivieri, Anna Mondino, Matteo Chinello, et al.
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