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Atherosclerosis Plus|July 6, 2026
Cholesterol in amyotrophic lateral sclerosis: a bystander, a biomarker, or a target?Matteo Farè, Chiara Comi, Giulia Susanna Ferrero, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1989
Effectiveness of steroid therapy in different stages of membranous nephropathyG Fuiano, P Stanziale, M Balletta, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 28, 2016
Reading, writing, and reserve: Literacy activities are linked to hippocampal volume and memory in multiple sclerosisJames F Sumowski, Maria A Rocca, Victoria M Leavitt, et al.
Frontiers in Neurology|December 6, 2024
Cardiac risk and myocardial fibrosis assessment with cardiac magnetic resonance in patients with myotonic dystrophyElena Abati, Claudia Alberti, Valentina Tambè, et al.
Microbiology Resource Announcements|May 31, 2022
Draft Genome Sequences of Eight Bacilli Isolated from an Ancient Roman AmphoraAndrea Colautti, Giuseppe Comi, Emanuele De Paoli, et al.
Genes|November 25, 2023
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature ReviewMichele Lombardi, Lucia Corrado, Beatrice Piola, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|January 19, 2023
[Malnutrition and dialytic adequacy in patients on peritoneal dialysis: two sides of the same coin?]Giuseppe Leonardi, Maria Grazia Arcidiacono, Irma Figlia, et al.
Journal of Personalized Medicine|January 21, 2023
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular CharacterizationMichela Ripolone, Simona Zanotti, Laura Napoli, et al.
Human Mutation|November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletionsAlessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Therapeutic Advances in Neurological Disorders|May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophiesDaniela Piga, Sabrina Salani, Francesca Magri, et al.
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