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Minerva Anestesiologica|November 1, 1993
[Carbon dioxide measurement in neuroanesthesia]F M Pelagalli, M PicciniAutoimmunity Reviews|July 10, 2003
Dosage and characterization of circulating DNA: present usage and possible applications in systemic autoimmune disordersM Galeazzi, G Morozzi, M Piccini, et al.American Journal of Nephrology|August 26, 1999
Evidence for genetic heterogeneity in benign familial hematuriaM Piccini, G Casari, J Zhou, et al.Muscle & Nerve|September 17, 1999
Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophyF Vitelli, M Villanova, A Malandrini, et al.Genomics|March 2, 1999
Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME)F Vitelli, M Piccini, F Caroli, et al.Genomics|September 24, 1999
KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologsM Piccini, F Vitelli, M Seri, et al.Annals of the Rheumatic Diseases|June 15, 2004
Simvastatin reduces MMP-3 level in interleukin 1beta stimulated human chondrocyte cultureP E Lazzerini, P L Capecchi, F Nerucci, et al.Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.Journal of Medical Genetics|May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?J J Jonsson, A Renieri, P G Gallagher, et al.Physical Review Letters|September 27, 2024
Search for Leptonic Decays of Dark Photons at NA62E Cortina Gil, J Jerhot, A Kleimenova, et al.Pageof 9