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Veterinary Parasitology|September 12, 2008
Efficiency of a recombinant MSA-2c-based ELISA to establish the persistence of antibodies in cattle vaccinated with Babesia bovisMaría F Bono, Atilio J Mangold, María E Baravalle, et al.Annals of Neurology|November 18, 1998
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron geneA Gambardella, R Mazzei, A Toscano, et al.Acta Neurologica Scandinavica|January 7, 2004
Gene conversion events in adult-onset spinal muscular atrophyR Mazzei, A Gambardella, F L Conforti, et al.Neurology|May 1, 1996
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large familyA Quattrone, A Gambardella, F Bono, et al.Annals of Neurology|February 9, 2000
Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjögren syndromeU Aguglia, G Annesi, G Pasquinelli, et al.The International Journal of Neuroscience|May 16, 2017
Plasma butyrylcholinesterase activity: a possible biomarker for differential diagnosis between Alzheimer's disease and dementia with Lewy bodies?N D Josviak, M S Batistela, R K M Souza, et al.Neurochemistry International|January 28, 2015
Butyrylcholinesterase: K variant, plasma activity, molecular forms and rivastigmine treatment in Alzheimer's disease in a Southern Brazilian populationG F Bono, D P Simão-Silva, M S Batistela, et al.Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.Neurology|January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern ItalyM Muglia, M Zappia, V Timmerman, et al.Nature|August 11, 1998
Role of HIF-1alpha in hypoxia-mediated apoptosis, cell proliferation and tumour angiogenesisP Carmeliet, Y Dor, J M Herbert, et al.Pageof 11