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1
von Cappellari, Manuel ; Bonetti, Bruno ; Baracchini, Claudio ; et al.
Neurological Sciences. 44(6):2033-2039
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2
von Aurora Fusto ; Denise Cassandrini ; Chiara Fiorillo ; et al.
Acta Neuropathologica Communications, Vol 10, Iss 1, Pp 1-20 (2022)
Schlagworte: RYR1-related myopathies; Central core disease; Multi-minicore disease; Genotype–phenotype correlations; Neuromuscular disorder; Protein modelling; Neurology. Diseases of the nervous system; RC346-429
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3
von Cappellari, Manuel ; Bonetti, Bruno ; Baracchini, Claudio ; et al.
Neurological Sciences. 44(10):3769-3769
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4
von Guglielmi, Valeria ; Vattemi, Gaetano ; Gualandi, Francesca ; et al.
In Molecular Genetics and Metabolism September-October 2013 110(1-2):162-169
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5
von Catteruccia, Michela ; Fattori, Fabiana ; Codemo, Valentina ; et al.
In Neuromuscular Disorders March 2013 23(3):229-238
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6
von Campagnolo, Marta ; Fiorenzato, Eleonora ; Musso, Giulia ; et al.
In Journal of the Neurological Sciences 15 September 2025 476
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7
von Fattori, Fabiana ; Maggi, Lorenzo ; Bruno, Claudio ; et al.
Journal of Neurology: Official Journal of the European Neurological Society. July 2015 262(7):1728-1740
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8
von Zara, Gabriella ; Codemo, Valentina ; Palmieri, Arianna ; et al.
Neurological Sciences: Official Journal of the Italian Neurological Society. February 2012 33(1):133-135
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9
von Fattori, F ; Maggi, L ; Bruno, C ; et al.
Schlagworte: Algorithm; Centronuclear; Congenital myopathy; DNM2; RYR1; Adolescent; Adult; Age of Onset; Aged; Child; Child, Preschool; Cohort Studie; Connectin; Dynamin II; Female; Genetic Association Studie; Genetic Predisposition to Disease; Human; Infant; Infant, Newborn; Italy; Male; Middle Aged; Muscle, Skeletal; Mutation; Myopathies, Structural, Congenital; Phenotype; Protein Tyrosine Phosphatases, Non-Receptor; Ryanodine Receptor Calcium Release Channel; Young Adult; info:eu-repo/semantics/article
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10
von Catteruccia, M ; Fattori, F ; Codemo, V ; et al.
Schlagworte: Centronuclear myopathy; DNM2; Muscle MRI; Somatic mosaicism; ‘Necklace’ fiber; 'Necklace' fiber; Adolescent; Adult; Child; Child, Preschool; Dynamin II; Female; Human; Italy; Magnetic Resonance Imaging; Male; Middle Aged; Mosaicism; Muscle, Skeletal; Myopathies, Structural, Congenital; Phenotype; Mutation; info:eu-repo/semantics/article
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11
von Ruggeri, Mirella ; Bonetto, Chiara ; Lasalvia, Antonio ; et al.
Schlagworte: First-episode psychosi; Early psychosi; Cognitive behavioral therapy; Psychosocial intervention; Assertive community treatment; Family intervention
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