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Annals of Neurology|August 9, 2007
Phenotypic characterization of hypomyelination and congenital cataractRoberta Biancheri, Federico Zara, Claudio Bruno, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 1, 2002
Altered aquaporin-4 expression in human muscular dystrophies: a common feature?Antonio Frigeri, Grazia Paola Nicchia, Silvia Repetto, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 27, 2007
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutationRoberta Biancheri, Andrea Rossi, Giannina Alpigiani, et al.
Der Internist|June 18, 2021
[Diagnostics and treatment of statin-associated muscle symptoms]Ursula Kassner, Stefanie Grunwald, Dominik Spira, et al.
Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.
Respiratory Medicine|October 4, 2016
Respiratory pattern in a FSHD pediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Muscle & Nerve|March 31, 2004
Motor function-muscle strength relationship in spinal muscular atrophyLuciano Merlini, Enrico Bertini, Carlo Minetti, et al.
Neuropediatrics|December 21, 2012
Magnetic resonance imaging "tigroid pattern" in Alexander diseaseRoberta Biancheri, Andrea Rossi, Isabella Ceccherini, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 16, 2023
Aberrant Adenosine Triphosphate Release and Impairment of P2Y2-Mediated Signaling in SarcoglycanopathiesAndrea Benzi, Serena Baratto, Cecilia Astigiano, et al.
Neuromuscular Disorders : NMD|February 4, 2009
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1Roberta Biancheri, Marianna Ciccolella, Andrea Rossi, et al.
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