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Journal of the Neurological Sciences|October 16, 2007
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiencyS Corti, A Bordoni, D Ronchi, et al.Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|December 6, 2013
Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patientS Lucchiari, G Ulzi, F Magri, et al.Neurology|October 15, 2003
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domainR Del Bo, A Bordoni, M Sciacco, et al.American Journal of Human Genetics|April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathyO Musumeci, A L Andreu, S Shanske, et al.American Journal of Medical Genetics|April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean areaS Lucchiari, I Fogh, A Prelle, et al.Cellular and Molecular Life Sciences : CMLS|November 8, 2008
Stem cell therapy in strokeF Locatelli, A Bersano, E Ballabio, et al.Journal of the Neurological Sciences|May 12, 2009
Transthyretin Asn90 variant: amyloidogenic or non-amyloidogenic roleA Bersano, R Del Bo, E Ballabio, et al.Journal of Cellular and Molecular Medicine|December 18, 2009
Growth factors in ischemic strokeS Lanfranconi, F Locatelli, S Corti, et al.Science (New York, N.Y.)|August 5, 2000
Role of adenine nucleotide translocator 1 in mtDNA maintenanceJ Kaukonen, J K Juselius, V Tiranti, et al.Heredity|May 3, 2012
An evolutionary history of the selectin gene cluster in humansM Fumagalli, M Fracassetti, R Cagliani, et al.Pageof 10