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American Journal of Medical Genetics|May 20, 1999
Strong similarities of the FMR1 mutation in multiple tissues: postmortem studies of a male with a full mutation and a male carrier of a premutationF Tassone, R J Hagerman, L W Gane, et al.Journal of Endocrinological Investigation|May 27, 2009
B-type natriuretic peptide levels and insulin resistance in patients with severe ischemic myocardial dysfunctionF Tassone, L Gianotti, F Rolfo, et al.Clinical Genetics|September 27, 2012
Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriersY Liu, T I Winarni, L Zhang, et al.Biochemistry|December 19, 1995
A noncanonical tertiary conformation of a human mitochondrial transfer RNAM A Leehey, C A Squassoni, M W Friederich, et al.Journal of Endocrinological Investigation|December 2, 2015
Mild primary hyperparathyroidism as defined in the Italian Society of Endocrinology's Consensus Statement: prevalence and clinical featuresE Castellano, F Tassone, R Attanasio, et al.Annales D'Endocrinologie|May 8, 2002
Neuroendocrine and metabolic determinants of the adaptation of GH/IGF-I axis to obesityM Maccario, F Tassone, S Grottoli, et al.Mini Reviews in Medicinal Chemistry|February 3, 2007
Ghrelin and other gastrointestinal peptides involved in the control of food intakeF Tassone, F Broglio, L Gianotti, et al.Journal of Neural Transmission. Supplementum|February 10, 2000
Gene expression relevant to Down syndrome: problems and approachesF Tassone, R Lucas, D Slavov, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 30, 2006
Tremor/ataxia syndrome and fragile X premutation: diagnostic caveatsD Z Loesch, L Litewka, A Churchyard, et al.American Journal of Medical Genetics. Supplement|January 1, 1990
Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomiesC Brahe, F Tassone, A Moscetti, et al.Pageof 16