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Journal of the American Heart Association|August 12, 2016
Consistency of Hemoglobin A1c Testing and Cardiovascular Outcomes in Medicare Patients With DiabetesPhilip P Goodney, Karina A Newhall, Kimon Bekelis, et al.
Journal of Alzheimer'S Disease : JAD|September 17, 2016
Growth Arrest Specific 6 Concentration is Increased in the Cerebrospinal Fluid of Patients with Alzheimer's DiseasePier Paolo Sainaghi, Mattia Bellan, Franco Lombino, et al.
Scientific Reports|December 5, 2023
Porcine milk exosomes modulate the immune functions of CD14+ monocytes in vitroGabriela Ávila Morales, Daria De Leonardis, Joel Filipe, et al.
Brain : a Journal of Neurology|January 23, 2003
Evidence for widespread axonal damage at the earliest clinical stage of multiple sclerosisM Filippi, M Bozzali, M Rovaris, et al.
Journal of Dairy Science|November 22, 2021
Identification of rare genetic variants of the αS-caseins in milk from native Norwegian dairy breeds and comparison of protein composition with milk from high-yielding Norwegian Red cowsN R Roin, L B Larsen, I Comi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 1999
Peripheral levels of caspase-1 mRNA correlate with disease activity in patients with multiple sclerosis; a preliminary studyR Furlan, M Filippi, A Bergami, et al.
Gene Therapy|August 18, 2001
Fibroblast growth factor-II gene therapy reverts the clinical course and the pathological signs of chronic experimental autoimmune encephalomyelitis in C57BL/6 miceF Ruffini, R Furlan, P L Poliani, et al.
Cerebral Cortex (New York, N.Y. : 1991)|November 19, 2011
Wnt signaling has opposing roles in the developing and the adult brain that are modulated by Hipk1Cinzia Marinaro, Maria Pannese, Franziska Weinandy, et al.
Human Brain Mapping|November 29, 2007
Structural and functional MRI correlates of Stroop control in benign MSMaria A Rocca, Paola Valsasina, Antonia Ceccarelli, et al.
Journal of the Neurological Sciences|January 3, 2006
Congenital muscular dystrophy with muscle inflammation alpha dystroglycan glycosylation defect and no mutation in FKRP geneCostanza Lamperti, Rachele Cagliani, Patrizia Ciscato, et al.
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