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Clinical Genetics|February 28, 2004
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like featuresC Pescucci, I Meloni, M Bruttini, et al.
Minerva Cardioangiologica|March 1, 1990
[Isthmic coarctation of the aorta. Description of an anomalous case]F Mascoli, G Anania, T Virgili, et al.
Seizure|April 11, 2008
Status epilepticus in epileptic patients. Related syndromes, precipitating factors, treatment and outcome in a video-EEG population-based studyC Di Bonaventura, F Mari, N Vanacore, et al.
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.
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