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Clinical Case Reports|February 14, 2015
Peripheral blood hemophagocytosis in an unusual lymphomaAlberto Fragasso, Clara Mannarella, Angela Ciancio, et al.
Mutation Research|March 12, 2004
A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndromeValentina Gatta, Oronzo Scarciolla, Massimo Cupaioli, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex"Marco Castori, Oronzo Scarciolla, Silvia Morlino, et al.
Thescientificworldjournal|April 7, 2012
Holotranscobalamin is a useful marker of vitamin B12 deficiency in alcoholicsAlberto Fragasso, Clara Mannarella, Angela Ciancio, et al.
Muscle & Nerve|February 28, 2006
Familial idiopathic hyper-CK-emia: an underrecognized conditionMargherita Capasso, Maria Vittoria De Angelis, Antonio Di Muzio, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 5, 2007
Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangementsOronzo Scarciolla, Francesco Brancati, Enza Maria Valente, et al.
Human Mutation|December 13, 2006
Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrumRoberta Marongiu, Francesco Brancati, Angelo Antonini, et al.
European Journal of Internal Medicine|January 18, 2011
Myocardial iron overload assessed by magnetic resonance imaging (MRI)T2* in multi-transfused patients with thalassemia and acquired anemiasAlberto Fragasso, Angela Ciancio, Clara Mannarella, et al.
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