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Pediatric Reports|February 20, 2026
Integrating the Genomic Revolution into Newborn Screening: Current Challenges and Future PerspectivesAlbina Tummolo, Emanuela Ponzi, Simonetta Simonetti, et al.
Pediatric Reports|March 24, 2026
Correction: Tummolo et al. Integrating the Genomic Revolution into Newborn Screening: Current Challenges and Future Perspectives. Pediatr. Rep. 2026, 18, 14Albina Tummolo, Emanuela Ponzi, Simonetta Simonetti, et al.
Diagnostics (Basel, Switzerland)|April 23, 2020
Combining Point-of-Care Diagnostics and Internet of Medical Things (IoMT) to Combat the COVID-19 PandemicTing Yang, Mattia Gentile, Ching-Fen Shen, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|December 2, 2015
Pulmonary alveolar microlithiasis: review of the 1022 cases reported worldwideGiuseppe Castellana, Giorgio Castellana, Mattia Gentile, et al.
European Journal of Pediatrics|January 28, 2014
Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literatureLucia Margari, Anna Linda Lamanna, Francesco Craig, et al.
Systems Biology in Reproductive Medicine|August 14, 2015
The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotypeRosa Santacroce, Roberta Trunzo, Angelica Leccese, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|March 17, 2006
Immunohistochemical mismatch repair proteins expression in colorectal cancerAnna Maria Valentini, Raffaele Armentano, Michele Pirrelli, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 29, 2021
Prenatal diagnosis of Pfeiffer syndrome and role of three-dimensional ultrasound: case report and review of literatureAntonella Vimercati, Claudiana Olivieri, Miriam Dellino, et al.
Case Reports in Genetics|February 4, 2026
The Ketogenic Diet in the Neonatal Intensive Care Setting: The Case of a Preterm Newborn With Mitochondrial DNA Depletion Syndrome Type 13 (MTDPS13)Gabriele D'Amato, Mattia Gentile, Rossella Carella, et al.
Prenatal Diagnosis|November 9, 2002
Prenatal diagnosis of ductus venosus agenesis and its association with cytogenetic/congenital anomaliesPaolo Volpe, Maurizio Marasini, Gilda Caruso, et al.
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