COMISI, FRANCESCO FABRIZIO

COMISI, FRANCESCO FABRIZIO  

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Titolo Data di pubblicazione Autore(i) Rivista Editore
Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies 1-gen-2025 Comisi, F.; Fusco, C.; Mura, R.; Cerruto, C.; D'Agruma, L.; Carnazzo, S.; Castori, M.; Savasta, S. AMERICAN JOURNAL OF MEDICAL GENETICS. PART A -
Rethinking Otorhinolaryngologic Care Pathways in Children with Down Syndrome: A Multidisciplinary Framework for Early Diagnosis and Management 1-gen-2025 Comisi, F. F.; Esposito, E.; Savasta, S. JOURNAL OF CLINICAL MEDICINE -
PPP2R5D-Related Neurodevelopmental Disorder and Multiple Haemangiomas: A Novel Phenotypic Trait? 1-gen-2024 Comisi, Francesco; Soddu, Consolata; Lai, Francesco; Marica, Monica; Lorrai, Michela; Mancuso, Giancarlo; Giglio, Sabrina; Savasta, Salvatore PEDIATRIC REPORTS -
Pyridostigmine as a therapeutic option for pediatric gastrointestinal dysmotilities in ATR-X syndrome. Case report and literature review 1-gen-2024 Comisi, F. F.; Soddu, C.; Corpino, M.; Marica, M.; Cacace, R.; Foiadelli, T.; Savasta, S. FRONTIERS IN PEDIATRICS -