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Human Genetics|February 1, 1997
Two novel PAH gene mutations detected in Italian phenylketonuric patientsA Argiolas, P Bosco, F Calì, et al.
The Journal of International Medical Research|January 1, 1996
Granulocyte-colony stimulating factor and erythropoietin therapy in children with human immunodeficiency virus infectionG V Zuccotti, A Plebani, G Biasucci, et al.
The Journal of Vascular Access|February 2, 2019
A novel ultrasound-guided approach to the axillary vein: Oblique-axis view combined with in-plane punctureFabrizio Brescia, Daniele G Biasucci, Fabio Fabiani, et al.
The Journal of Vascular Access|November 18, 2017
Targeting zero catheter-related bloodstream infections in pediatric intensive care unit: a retrospective matched case-control studyDaniele G Biasucci, Mauro Pittiruti, Alessandra Taddei, et al.
The Journal of Vascular Access|April 5, 2021
Neo-ECHOTIP: A structured protocol for ultrasound-based tip navigation and tip location during placement of central venous access devices in neonatesGiovanni Barone, Mauro Pittiruti, Daniele G Biasucci, et al.
European Journal of Nutrition|September 3, 2010
The presence of ochratoxin A in cord serum and in human milk and its correspondence with maternal dietary habitsG Biasucci, G Calabrese, R Di Giuseppe, et al.
Minerva Anestesiologica|July 22, 2025
Body composition determined with computed tomography at ICU admission as a potential long-term outcome assessment tool in critically ill patients: a post-hoc analysis of a prospective, observational studyCristian Deana, Lorenzo Cereser, Luigi Nardone, et al.
The Journal of International Medical Research|June 3, 2010
Nutritional profiles in a public health perspective: a critical reviewF Foltran, E Verduci, M Ghidina, et al.
The Journal of Hospital Infection|April 7, 2022
Catheter salvage strategies in children with central venous catheter-related or -associated bloodstream infections: a systematic review and meta-analysisD Buonsenso, G Salerno, G Sodero, et al.
FEBS Letters|October 22, 1998
Structure and mutation analysis of the glycogen storage disease type 1b geneP Marcolongo, V Barone, G Priori, et al.
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