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Multidisciplinary Respiratory Medicine|November 8, 2021
Emergency Department Visits for allergy related-disorders among children: experience of a single Italian hospital during the first wave of the COVID-19 pandemicMarina Attanasi, Annamaria Porreca, Giuseppe Francesco Sferrazza Papa, et al.
Birth Defects Research|May 24, 2023
Neonatal diagnosis of circumferential skin creasesChiara Cauzzo, Valentina Chiavaroli, Chiara Palka Bayard de Volo, et al.
Congenital Anomalies|June 5, 2023
Perinatal diagnosis of congenital urogenital sinus abnormalityRiccardo Fiorentino, Saverio La Bella, Valentina Chiavaroli, et al.
Epilepsy & Behavior : E&B|January 14, 2011
Long term outcome in children affected by absence epilepsy with onset before the age of three yearsAlberto Verrotti, Cristina Olivieri, Sergio Agostinelli, et al.
BMC Medical Genetics|June 3, 2014
Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndromeStefano Stagi, Elisabetta Lapi, Maria Gabriella D'Avanzo, et al.
Developmental Medicine and Child Neurology|January 5, 2008
Levetiracetam in juvenile myoclonic epilepsy: long-term efficacy in newly diagnosed adolescentsAlberto Verrotti, Caterina Cerminara, Giangennaro Coppola, et al.
Children (Basel, Switzerland)|October 26, 2024
Acute Respiratory Failure in Children: A Clinical Update on DiagnosisBeatrice Panetti, Ilaria Bucci, Armando Di Ludovico, et al.
Frontiers in Pediatrics|January 26, 2023
Use of lung ultrasound in school-aged children with wheezingMarina Attanasi, Simone Sferrazza Papa, Annamaria Porreca, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|July 22, 2020
Role of the KCNJ Gene Variants in the Clinical Outcome of Type 1 DiabetesAnnalisa Blasetti, Valeria Castorani, Laura Comegna, et al.
Pediatrics|December 7, 2011
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairmentChiara Palka, Melissa Alfonsi, Angelika Mohn, et al.
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