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BMC Evolutionary Biology|June 3, 2009
A complex selection signature at the human AVPR1B geneRachele Cagliani, Matteo Fumagalli, Uberto Pozzoli, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 19, 2008
Charcot-Marie-Tooth type 1a in a child with Long QT syndromeLuciana Losito, Marta De Rinaldis, Leonarda Gennaro, et al.Archives of Neurology|November 16, 2005
Muscle coenzyme Q10 level in statin-related myopathyCostanza Lamperti, Ali B Naini, Valeria Lucchini, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 28, 2008
Migraine, stroke and patent foramen ovale: a dangerous trio?Gianfranco Butera, Elio Agostoni, Giuseppe Biondi-Zoccai, 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.Muscle & Nerve|August 20, 2004
Developmental and tissue-specific regulation of a novel dysferlin isoformSabrina Salani, Sabrina Lucchiari, Francesco Fortunato, et al.Cellular and Molecular Life Sciences : CMLS|March 4, 2020
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1)Martina G L Perego, Noemi Galli, Monica Nizzardo, et al.Ageing Research Reviews|September 24, 2020
Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementiaDelia Gagliardi, Gianluca Costamagna, Michela Taiana, et al.Journal of the Neurological Sciences|September 11, 2002
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patientsRoberto Del Bo, Andreina Bordoni, Filippo Martinelli Boneschi, et al.Neuroscience Letters|May 22, 2003
Altered glutamate uptake in peripheral tissues from Down syndrome patientsBarbara Begni, Laura Brighina, Lorenzo Fumagalli, et al.Pageof 34