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Frontiers in Pediatrics|October 4, 2021
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult PatientFrancesca Conti, Arianna Catelli, Cristina Cifaldi, et al.
Frontiers in Pediatrics|July 26, 2021
Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult PatientFrancesca Conti, Arianna Catelli, Cristina Cifaldi, et al.
COPD|May 5, 2015
Italian registry of patients with alpha-1 antitrypsin deficiency: general data and quality of life evaluationMaurizio Luisetti, Ilaria Ferrarotti, Luciano Corda, et al.
International Journal of Molecular Sciences|October 2, 2020
An Analysis of Clinical, Surgical, Pathological and Molecular Characteristics of Endometrial Cancer According to Mismatch Repair Status. A Multidisciplinary ApproachGiulia Dondi, Sara Coluccelli, Antonio De Leo, et al.
Molecular Cytogenetics|October 3, 2012
Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genesCristina Marletta, Roberto Valli, Barbara Pressato, et al.
Journal of Translational Medicine|July 5, 2024
Interplay between WNT/PI3K-mTOR axis and the microbiota in APC-driven colorectal carcinogenesis: data from a pilot study and possible implications for CRC preventionFloriana Jessica Di Paola, Chiara Alquati, Gabriele Conti, et al.
Clinical Genetics|December 21, 2024
Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily PracticeGiovanni Innella, Emanuele Coccia, Carlotta Pia Cristalli, et al.
European Urology|July 20, 2025
Single-port Antegrade Robotic Lymphadenectomy: A Novel Minimally Invasive Approach to Treat Lymph Nodes in Men with Penile CancerAldo Brassetti, Alfredo Maria Bove, Flavia Proietti, et al.
Sleep Medicine|April 9, 2014
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1Keivan Kaveh Moghadam, Fabio Pizza, Caterina Tonon, et al.
International Journal of Molecular Sciences|May 27, 2023
Multi-Gene Next-Generation Sequencing Panel for Analysis of BRCA1/BRCA2 and Homologous Recombination Repair Genes Alterations Metastatic Castration-Resistant Prostate CancerThais Maloberti, Antonio De Leo, Sara Coluccelli, et al.
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