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European Journal of Clinical Investigation|April 27, 2010
A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patientM Dagnino, G Caridi, M Marsciani, et al.Pediatric Surgery International|February 27, 2004
Laparoscopic antireflux surgery in neurologically impaired childrenM Lima, M Bertozzi, G Ruggeri, et al.British Journal of Haematology|June 1, 1993
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocketG Marchetti, P Patracchini, D Gemmati, et al.The New England Journal of Medicine|September 14, 2000
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery diseaseD Girelli, C Russo, P Ferraresi, et al.Archives of Disease in Childhood|October 1, 1983
Neonatal screening for congenital adrenal hyperplasiaE Cacciari, A Balsamo, A Cassio, et al.Virology|May 18, 1999
Potyvirus helper component-proteinase self-interaction in the yeast two-hybrid system and delineation of the interaction domain involvedS Urcuqui-Inchima, J Walter, G Drugeon, et al.Human Genetics|November 1, 1993
Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic regionF Bernardi, P Patracchini, D Gemmati, et al.Physical Chemistry Chemical Physics : PCCP|November 13, 2015
Evidence for localized moment picture in Mn-based Heusler compoundsJ Karel, F Bernardi, C Wang, et al.Journal of Thrombosis and Haemostasis : JTH|July 12, 2018
The chaperone-like sodium phenylbutyrate improves factor IX intracellular trafficking and activity impaired by the frequent p.R294Q mutationS Pignani, A Todaro, M Ferrarese, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1996
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasmaF Bernardi, G Marchetti, M Pinotti, et al.Pageof 34