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Journal of Neuropathology and Experimental Neurology|October 10, 2009
Mitochondrial ferritin in the substantia nigra in restless legs syndromeAmanda M Snyder, XinSheng Wang, Stephanie M Patton, et al.
Frontiers in Oncology|April 18, 2022
Iron Administration Overcomes Resistance to Erastin-Mediated Ferroptosis in Ovarian Cancer CellsAnna Martina Battaglia, Alessandro Sacco, Ida Daniela Perrotta, et al.
Cell Death & Disease|February 26, 2022
Massive iron accumulation in PKAN-derived neurons and astrocytes: light on the human pathological phenotypePaolo Santambrogio, Maddalena Ripamonti, Anna Cozzi, et al.
Pharmaceutics|January 21, 2023
PPAR Gamma Agonist Leriglitazone Recovers Alterations Due to Pank2-Deficiency in hiPS-Derived AstrocytesPaolo Santambrogio, Anna Cozzi, Ivano Di Meo, et al.
Haematologica|October 14, 2003
Identification of two novel mutations in the 5'-untranslated region of H-ferritin using denaturing high performance liquid chromatography scanningLaura Cremonesi, Barbara Foglieni, Isabella Fermo, et al.
American Journal of Hematology|January 5, 2017
Unexplained isolated hyperferritinemia without iron overloadGiulia Ravasi, Sara Pelucchi, Raffaella Mariani, et al.
The Journal of Biological Chemistry|February 18, 2010
Mutant ferritin L-chains that cause neurodegeneration act in a dominant-negative manner to reduce ferritin iron incorporationSara Luscieti, Paolo Santambrogio, Béatrice Langlois d'Estaintot, et al.
Haematologica|June 30, 2011
Over-expression of mitochondrial ferritin affects the JAK2/STAT5 pathway in K562 cells and causes mitochondrial iron accumulationPaolo Santambrogio, Benedetta Gaia Erba, Alessandro Campanella, et al.
Human Mutation|January 6, 2006
Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolismFrancesca Ferrari, Barbara Foglieni, Paolo Arosio, et al.
British Journal of Haematology|October 31, 2002
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3)Mario Cazzola, Laura Cremonesi, Maria Papaioannou, et al.
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