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BMJ Open|February 28, 2013
Exposure to benzene and childhood leukaemia: a pilot case-control studySusanna Lagorio, Daniela Ferrante, Alessandra Ranucci, et al.Journal of the Peripheral Nervous System : JPNS|February 28, 2022
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathyBianca R Grosz, Igor Stevanovski, Sara Negri, et al.La Medicina Del Lavoro|April 28, 2017
Methodology to define biological reference values in the environmental and occupational fields: the contribution of the Italian Society for Reference Values (SIVR)Maria Cristina Aprea, Maria Luisa Scapellato, Maria Carmen Valsania, et al.Cells|February 10, 2021
Selective Targeting of Cancer-Associated Fibroblasts by Engineered H-Ferritin Nanocages Loaded with NavitoclaxLeopoldo Sitia, Arianna Bonizzi, Serena Mazzucchelli, et al.Journal of the American College of Cardiology|December 10, 2013
Subclinical abnormalities in sarcoplasmic reticulum Ca(2+) release promote eccentric myocardial remodeling and pump failure death in response to pressure overloadSimon Sedej, Albrecht Schmidt, Marco Denegri, et al.International Journal of Molecular Sciences|August 26, 2022
Bisdemethoxycurcumin (BDC)-Loaded H-Ferritin-Nanocages Mediate the Regulation of Inflammation in Alzheimer's Disease PatientsStella Gagliardi, Marta Truffi, Veronica Tinelli, et al.Journal of Nanobiotechnology|November 17, 2024
Exploring the anti-inflammatory effects of curcumin encapsulated within ferritin nanocages: a comprehensive in vivo and in vitro study in Alzheimer's diseaseCarlo Morasso, Marta Truffi, Veronica Tinelli, et al.Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Gene-Pseudogene Inversions as a Hidden Source of Missing HeritabilityIlaria Quartesan, Stefano Facchini, Arianna Manini, et al.Nature Genetics|May 28, 2020
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.Nature Genetics|May 6, 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.Pageof 5