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European Journal of Medical Genetics|March 25, 2026
Horizontal gaze palsy with progressive scoliosis (HGPPS): expanding ROBO3 molecular spectrum and refining clinical-neuroimaging phenotypesMohammad Sadegh Shams Nosrati, Ferruccio Romano, Alireza Dostmohammadi, et al.
International Journal of Molecular Sciences|June 13, 2025
Blurred by a "Puff of Smoke"-A Case-Based Review on the Challenging Recognition of Coexisting CNS Demyelinating Disease and Moyamoya AngiopathyIsabella Canavero, Nicola Rifino, Carlo Antozzi, et al.
International Journal of Food Sciences and Nutrition|May 25, 2018
Nutritional characterisation of Zambian <i>Moringa oleifera</i>: acceptability and safety of short-term daily supplementation in a group of malnourished girlsMichela Barichella, Gianni Pezzoli, Samanta A Faierman, et al.
The Journal of Infection|February 20, 2026
The DENGVAC Study: Preliminary Findings on the Immunogenicity of the TAK-003 Dengue VaccineAlessandra D'Abramo, Francesca Colavita, Laura Ponzetta, et al.
Human Mutation|April 14, 2025
Somatic Double Inactivation of <i>NF1</i> Associated with NF1-Related Pectus Excavatum DeformityCristina Chelleri, Marcello Scala, Patrizia De Marco, et al.
Cancers|March 29, 2023
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of <i>RNF213</i>Marzia Ognibene, Marcello Scala, Michele Iacomino, et al.
Frontiers in Oncology|April 6, 2026
HLH and spinal neurofibroma: a single case report in a patient with DiGeorge syndromeRamona Tallone, Concetta Micalizzi, Maura Faraci, et al.
Open Forum Infectious Diseases|January 28, 2021
Thymosin Alpha 1 Mitigates Cytokine Storm in Blood Cells From Coronavirus Disease 2019 PatientsClaudia Matteucci, Antonella Minutolo, Emanuela Balestrieri, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|September 10, 2025
Risk factors for persisting SARS-CoV-2 infection in patients with B-cell malignancies in the Omicron era: A multicenter cohort studyZeno Pasquini, Alice Toschi, Dino Gibertoni, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2024
Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorderAndrea Accogli, Young N Park, Guy M Lenk, et al.
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