B. Foglieni

发表

High Serum Levels of HDV RNA Are Predictors of Cirrhosis and Liver Cancer in Patients with Chronic Hepatitis Delta

G. Casazza, D. Prati, M. Colombo, 2014, PloS one.

Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients

M. Dean, R. Allikmets, M. Ferrari, 2001, Human Genetics.

Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms

D. Girelli, M. Ferrari, I. Fermo, 2004, Journal of Medical Genetics.

Scanning mutations of the 5′UTR regulatory sequence of l‐ferritin by denaturing high‐performance liquid chromatography: identification of new mutations

M. Cazzola, M. Ferrari, R. Paroni, 2003, British journal of haematology.

Prevalence and 9‐year incidence of hepatitis E virus infection among North Italian blood donors: Estimated transfusion risk

D. Prati, A. Colli, A. Berzuini, 2020, Journal of Viral Hepatitis.

Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.

J. Garcia-conde, A. Schmitt-Graeff, R. Paroni, 2003, Haematologica.

Evidence of Distinct Tumour-Propagating Cell Populations with Different Properties in Primary Human Hepatocellular Carcinoma

V. Mazzaferro, P. Rebulla, M. Cadamuro, 2011, PloS one.

Poor efficacy of nucleic acid testing in identifying occult HBV infection and consequences for safety of blood supply in Italy.

D. Prati, J. Allain, D. Candotti, 2015, Journal of hepatology.

Molecular diagnostics by microelectronic microchips

Maurizio Ferrari, Pierangelo Bonini, Laura Cremonesi, 2005, Expert review of molecular diagnostics.

International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

Casey S. Greene, Marco Carbone, Andrew Fraser, 2015, Nature Communications.

Beta-thalassemia microelectronic chip: a fast and accurate method for mutation detection.

Laura Cremonesi, Paolo Fortina, Maurizio Ferrari, 2004, Clinical chemistry.

A cluster of human immunodeficiency virus Type 1 recombinant form escaping detection by commercial genomic amplification assays

D. Rossi, D. Prati, J. Allain, 2011, Transfusion.

Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large‐scale analysis of disorders of iron metabolism

M. Cazzola, C. Beaumont, M. Ferrari, 2006, Human mutation.

The humoral immune response to SARS-CoV-2 mounts and is durable in symptomatic hemodialysis patients

F. Luzzaro, S. Viganò, V. La Milia, 2021, Nephrology, Dialysis and Transplantation.

A novel deletion of the l‐ferritin iron‐responsive element responsible for severe hereditary hyperferritinaemia–cataract syndrome

M. Cazzola, P. Arosio, M. Lazzarino, 2002, British journal of haematology.

Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of β-thalassemia

M. Ferrari, S. Galbiati, L. Cremonesi, 2008, Haematologica.

Single-nucleotide polymorphism and mutation identification by the nanogen microelectronic chip technology.

Maurizio Ferrari, Pierangelo Bonini, Laura Cremonesi, 2005, Methods in molecular medicine.

Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology.

Marco Seri, Roberto Ravazzolo, Alessandro Ferraris, 2002, Clinical chemistry.

Different Approaches for Noninvasive Prenatal Diagnosis of Genetic Diseases Based on PNA‐Mediated Enriched PCR

M. Ferrari, M. Chiari, F. Damin, 2006, Annals of the New York Academy of Sciences.

Feasibility Study for a Microchip‐Based Approach for Noninvasive Prenatal Diagnosis of Genetic Diseases

M. Ferrari, S. Galbiati, A. Piga, 2004, Annals of the New York Academy of Sciences.

A cluster of patients with recombinant B/F HIV‐1 infection: Epidemiological, clinical, and virological aspects

D. Prati, R. Rossotti, A. Orani, 2011, Journal of medical virology.

Plasmodium genome in blood donors at risk for malaria after several years of residence in Italy

D. Prati, J. Allain, A. Berzuini, 2014, Transfusion.

Integrated PCR amplification and detection processes on a Lab-on-Chip platform: a new advanced solution for molecular diagnostics

Sabrina Conoci, Salvatore Petralia, Laura Cremonesi, 2010, Clinical chemistry and laboratory medicine.

Analysis of ferritin genes in Parkinson disease.

J. Connor, M. Volontè, M. Ferrari, 2007, Clinical chemistry and laboratory medicine.

Single nucleotide polymorphism and mutation identification by microelectronic chip technology

M. Ferrari, S. Stenirri, L. Cremonesi, 2002 .

A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia.

M. Ferrari, S. Galbiati, L. Cremonesi, 2008, Methods in molecular biology.

Identification of two novel mutations in the 5'-untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning.

M. Ferrari, R. Paroni, I. Fermo, 2003, Haematologica.

Black blood matters.

C. Paccapelo, A. Berzuini, A. Gerosa, 2021, Blood transfusion = Trasfusione del sangue.

Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms

D. Girelli, M. Ferrari, I. Fermo, 2004, Journal of Medical Genetics.