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BMC Pediatrics|February 24, 2017
Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right triggerLuca Baroero, Paola Coppo, Laura Bertolino, et al.
Frontiers in Pediatrics|December 25, 2023
A single scalp nodule as the first presentation of acute lymphoblastic leukemia (KMT2A::MLLT3) in a healthy-appearing infant: a case reportFrancesco Pellegrino, Paola Coppo, Elena Barisone, et al.
Italian Journal of Pediatrics|January 9, 2016
Neonatal lupus erythematosus: a cutaneous cases based updateFrancesco Savino, Serena Viola, Valentina Tarasco, et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|December 19, 2017
Expression of miRNA 155, FOXP3 and ROR gamma, in children with moderate and severe atopic dermatitisMassimiliano Bergallo, Martina Accorinti, Ilaria Galliano, et al.
Annals of Pediatric Cardiology|February 12, 2024
Successful treatment of pulmonary arterial hypertension in a 2-month-old female infant with incontinentia pigmenti: A case reportMarta Marcia, Paola Coppo, Giuseppe Alberto Annoni, et al.
Pediatric Dermatology|November 23, 2012
Acute hemorrhagic edema of infancy: a troubling cutaneous presentation with a self-limiting courseFrancesco Savino, Maria M Lupica, Valentina Tarasco, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|August 6, 2024
Trichophyton erinacei infection in humans: a case report and a literature reviewEdoardo Cammarata, Nunzia Di Cristo, Chiara Airoldi, et al.
Clinical Genetics|January 28, 2021
A new case of Smith-Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowthDiana Carli, Giovanni Battista Ferrero, Anna Fusillo, et al.
Journal of Medical Genetics|January 27, 2025
Expanding the phenotypic spectrum of PROS: reclassifying isolated lateralised overgrowthAndrea Gazzin, Giuseppe Reynolds, Stefania Massuras, et al.
Genes, Chromosomes & Cancer|July 3, 2023
The somatic p.T81dup variant in AKT3 gene underlies a mild cerebral phenotype and expands the spectrum including capillary malformation and lateralized overgrowthMaria Luca, Marilidia Piglionica, Rosanna Bagnulo, et al.
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