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International Journal of Molecular Sciences|December 23, 2023
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy ControlsFrancesca Magri, Laura Napoli, Michela Ripolone, et al.
Frontiers in Neurology|March 1, 2024
Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysisSamah K Aburahma, Liqa A Rousan, Mohammad Shboul, et al.
Journal of Chemotherapy (Florence, Italy)|June 12, 2026
Cefiderocol for Stenotrophomonas maltophilia infections: real-world evidence from a multicenter study and a comprehensive literature reviewMichela Comi, Giulia Mancarella, Silvia Di Bari, et al.
Neurology|January 15, 2000
A conventional and magnetization transfer MRI study of the cervical cord in patients with MSM Filippi, M Bozzali, M A Horsfield, et al.
Multiple Sclerosis and Related Disorders|June 4, 2019
Caesarean section and infant formula feeding are associated with an earlier age of onset of multiple sclerosisGloria Dalla Costa, Marzia Romeo, Federica Esposito, et al.
Muscle & Nerve|May 1, 1983
Prospective study of X-linked progressive muscular dystrophy in CampaniaG Nigro, L I Comi, F M Limongelli, et al.
JAMA|May 1, 1996
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophiesL Politano, V Nigro, G Nigro, et al.
Journal of Human Hypertension|November 26, 2010
Olmesartan/amlodipine vs olmesartan/hydrochlorothiazide in hypertensive patients with metabolic syndrome: the OLAS studyF J Martinez-Martin, H Rodriguez-Rosas, I Peiro-Martinez, et al.
European Journal of Clinical Pharmacology|August 8, 2016
Polymorphisms of dopamine receptor genes and risk of visual hallucinations in Parkinson's patientsM Ferrari, C Comi, F Marino, et al.
Human Genetics|May 1, 2004
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotypeRachele Cagliani, Manuela Sironi, Emma Ciafaloni, et al.
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