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	1.	[2 years experience with periodic administration of intrathecal morphine to a patient with tumor pain]. [electronic resource] by Fiume, D Piccini, M Producer: 19850904 In: Minerva anestesiologica vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Carbon dioxide measurement in neuroanesthesia]. [electronic resource] by Pelagalli, F M Piccini, M Producer: 19940601 In: Minerva anestesiologica vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	3.	Early postoperative extramedullary MRI signal changes after ACDF: misinterpretations can be dangerous and misleading. Case report and review of the literature. [electronic resource] by Barbagallo, G Certo, F Princiotto, S Piccini, M Albanese, V Visocchi, M Producer: 20141203 In: Journal of neurosurgical sciences vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	4.	Dosage and characterization of circulating DNA: present usage and possible applications in systemic autoimmune disorders. [electronic resource] by Galeazzi, M Morozzi, G Piccini, M Chen, J Bellisai, F Fineschi, S Marcolongo, R Producer: 20030905 In: Autoimmunity reviews vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Evidence for genetic heterogeneity in benign familial hematuria. [electronic resource] by Piccini, M Casari, G Zhou, J Bruttini, M Volti, S L Ballabio, A Renieri, A Producer: 19991021 In: American journal of nephrology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy. [electronic resource] by Vitelli, F Villanova, M Malandrini, A Bruttini, M Piccini, M Merlini, L Guazzi, G Renieri, A Producer: 19991028 In: Muscle & nerve vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	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). [electronic resource] by Vitelli, F Piccini, M Caroli, F Franco, B Malandrini, A Pober, B Jonsson, J Sorrentino, V Renieri, A Producer: 19990524 In: Genomics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs. [electronic resource] by Piccini, M Vitelli, F Seri, M Galietta, L J Moran, O Bulfone, A Banfi, S Pober, B Renieri, A Producer: 19991122 In: Genomics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Simvastatin reduces MMP-3 level in interleukin 1beta stimulated human chondrocyte culture. [electronic resource] by Lazzerini, P E Capecchi, P L Nerucci, F Fioravanti, A Chellini, F Piccini, M Bisogno, S Marcolongo, R Laghi Pasini, F Producer: 20040827 In: Annals of the rheumatic diseases vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation. [electronic resource] by Piccini, M Vitelli, F Bruttini, M Pober, B R Jonsson, J J Villanova, M Zollo, M Borsani, G Ballabio, A Renieri, A Producer: 19980408 In: Genomics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Molecular diagnosis of Alport syndrome: the experience in Siena. [electronic resource] by Renieri, A Bruttini, M Piccini, M Bruno, M Cecconi, M Conti, M Coppo, R La Manna, A Trivelli, A De Marchi, M Ballabio, A Producer: 19980127 In: Contributions to nephrology vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome? [electronic resource] by Jonsson, J J Renieri, A Gallagher, P G Kashtan, C E Cherniske, E M Bruttini, M Piccini, M Vitelli, F Ballabio, A Pober, B R Producer: 19980630 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)