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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|February 1, 2013
Predictive modeling of cardiovascular complications in incident hemodialysis patientsJ Ion Titapiccolo, M Ferrario, C Barbieri, et al.American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.Minerva Cardioangiologica|October 1, 1989
[Retroesophageal right subclavian artery. Description of a clinical case]F Mascoli, T Virgili, P Carcoforo, et al.Minerva Cardioangiologica|May 1, 1989
[Effects of therapy with aminaftone on chronic venous and lymphatic stasis]D De Anna, F Mari, S Intini, et al.Clinical Genetics|June 6, 2003
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicismS Palmeri, F Mari, I Meloni, et al.Minerva Cardioangiologica|January 1, 1993
[Duplex scanner diagnosis of complete extracranial carotid artery obstruction: possibilities and limitations]F Mari, F Mascoli, E Gresta, et al.Minerva Cardioangiologica|November 1, 1991
[Visceral aneurysmal arterial pathology]G F Vettorello, F Mascoli, M C Taddia, et al.European Journal of Medical Genetics|March 28, 2009
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumbM Pollazzon, S Grosso, F T Papa, et al.Clinical Genetics|September 13, 2001
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardationA Malandrini, F Mari, S Palmeri, et al.Minerva Chirurgica|May 31, 1990
[Qualitative ultrasound analysis as a preliminary step in revascularization of the femoro-popliteal axis]F Mascoli, F Mari, M C Taddia, et al.Pageof 8