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Frontiers in Neurology|July 21, 2022
Clinical Features and Outcome of the Guillain-Barre Syndrome: A Single-Center 11-Year ExperienceFederica Ginanneschi, Fabio Giannini, Francesco Sicurelli, et al.
Rheumatology International|December 25, 2012
Human osteoarthritic chondrocytes exposed to extremely low-frequency electromagnetic fields (ELF) and therapeutic application of musically modulated electromagnetic fields (TAMMEF) systems: a comparative studyClaudio Corallo, Nila Volpi, Daniela Franci, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|July 28, 2010
Colchicine myopathy and neuromyopathy: two cases with different characteristicsLuca Cantarini, Nila Volpi, Mauro Galeazzi, et al.
Cells|September 14, 2024
CCDC78: Unveiling the Function of a Novel Gene Associated with Hereditary MyopathyDiego Lopergolo, Gian Nicola Gallus, Giuseppe Pieraccini, et al.
Biomedicines|July 29, 2023
Anti-Cytosolic 5'-Nucleotidase 1A in the Diagnosis of Patients with Suspected Idiopathic Inflammatory Myopathies: An Italian Real-Life, Single-Centre Retrospective StudyBrunetta Porcelli, Miriana d'Alessandro, Latika Gupta, et al.
Frontiers in Immunology|May 16, 2022
Variants Disrupting CD40L Transmembrane Domain and Atypical X-Linked Hyper-IgM Syndrome: A Case Report With Leishmaniasis and Review of the LiteratureBoaz Palterer, Lorenzo Salvati, Manuela Capone, et al.
Rheumatology (Oxford, England)|June 22, 2022
Accuracy of power Doppler ultrasonography in the diagnosis and monitoring of idiopathic inflammatory myopathiesEdoardo Conticini, Paolo Falsetti, Silvia Grazzini, et al.
Iscience|May 7, 2020
Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1G93A Mice Predates Disease Onset and Is A Promising Therapeutic TargetSilvia Scaricamazza, Illari Salvatori, Giacomo Giacovazzo, et al.
Nature Genetics|March 13, 2002
FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardationIlaria Meloni, Maddalena Muscettola, Martine Raynaud, et al.
Human Mutation|September 13, 2017
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathyVirginia Barone, Valeria Del Re, Alessandra Gamberucci, et al.
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