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Epilepsia|November 5, 2011
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutationsGuido Rubboli, Silvana Franceschetti, Samuel F Berkovic, et al.
BMC Musculoskeletal Disorders|December 29, 2022
Massive foreign body reaction and osteolysis following primary anterior cruciate ligament reconstruction with the ligament augmentation and reconstruction system (LARS): a case report with histopathological and physicochemical analysisLuca Ambrosio, Gianluca Vadalà, Rachele Castaldo, et al.
Frontiers in Endocrinology|December 5, 2022
Pituitary apoplexy and COVID-19 vaccination: a case report and literature reviewLudovica Aliberti, Irene Gagliardi, Roberta Rizzo, et al.
Epilepsia|February 22, 2023
IRF2BPL: A new genotype for progressive myoclonus epilepsiesCinzia Costa, Karen L Oliver, Carmen Calvello, et al.
Haematologica|March 9, 2004
Aberrant promoter methylation of multiple genes throughout the clinico-pathologic spectrum of B-cell neoplasiaDavide Rossi, Daniela Capello, Annunziata Gloghini, et al.
Cancers|December 11, 2022
Clinical Management of Long-Term Survivors after Classical Hodgkin Lymphoma and Diffuse Large B-Cell LymphomaAlessia Bari, Chiara Gerardi, Eleonora Allocati, et al.
Haematologica|October 5, 2006
Aberrant somatic hypermutation in transformation of follicular lymphoma and chronic lymphocytic leukemia to diffuse large B-cell lymphomaDavide Rossi, Eva Berra, Michaela Cerri, et al.
Endocrine|September 15, 2016
Proposal for a novel management of indeterminate thyroid nodules on the basis of cytopathological subclassesMartina Rossi, Sabrina Lupo, Roberta Rossi, et al.
Critical Care (London, England)|December 16, 2021
Flow Index accurately identifies breaths with low or high inspiratory effort during pressure support ventilationFilippo Albani, Federica Fusina, Gianni Ciabatti, et al.
Neurology|March 29, 2007
Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsH Lohi, J Turnbull, X C Zhao, et al.
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