Luciano Baronciani

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)

Anne Goodeve, Jeroen Eikenboom, Giancarlo Castaman et al. · Blood · 2006 · 397 citations · Full text

Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients

Augusto B. Federici, Pier Mannuccio Mannucci, Giancarlo Castaman et al. · Blood · 2008 · 258 citations

The ADAMTS13‐von Willebrand factor axis in COVID‐19 patients

Ilaria Mancini, Luciano Baronciani, Andrea Artoni et al. · Journal of Thrombosis and Haemostasis · 2020 · 234 citations · Full text

Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients

Luciano Baronciani, Giovanna Cozzi, Maria Teresa Canciani et al. · Blood Cells Molecules and Diseases · 2003 · 115 citations

Disease Mechanism, Genetic Disorder, Multiethnic Patients +11

Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia.

Luciano Baronciani, Ernest Beutler · Proceedings of the National Academy of Sciences · 1993 · 78 citations · Full text

Nt 1705, Genetics, Oligonucleotide Primers +20