Luciano Baronciani - Concepedia

Author

Luciano Baronciani

University of Milan ORCID

Also Known As

Baronciani, L, L Baronciani, L. BARONCIANI, L. Baronciani, LUCIANO BARONCIANI, Luciano Baronciani, Paolino Ninfali

138

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

University of Milan Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Ospedale Maggiore Scripps Research Institute University of Urbino

About

Luciano Baronciani is an author at University of Milan specializing in medicine, hematology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	21	654
2	Public Health	6	6	186
3	Biochemistry	6	6	160
4	Health Sciences	3	3	122
5	Natural Sciences	3	3	119

Luciano Baronciani

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
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, Blood	2006	397
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, Blood	2008	258
The ADAMTS13‐von Willebrand factor axis in COVID‐19 patients Ilaria Mancini, Luciano Baronciani, Andrea Artoni, Journal of Thrombosis and Haemostasis	2020	234
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients Luciano Baronciani, Giovanna Cozzi, Maria Teresa Canciani, Blood Cells Molecules and Diseases Disease MechanismGenetic DisorderMultiethnic PatientsMedicineInherited Metabolic Disease	2003	115
Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia. Luciano Baronciani, Ernest Beutler Proceedings of the National Academy of Sciences Nt 1705GeneticsOligonucleotide PrimersHuman PolymorphismMolecular Biology	1993	78
Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia. Luciano Baronciani, Ernest Beutler Journal of Clinical Investigation GeneticsDna AnalysisPathologyMolecular BiologyMolecular Genetics	1995	77
Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B Paquita Nurden, Giuliana Gobbi, Alan T. Nurden, Blood	2010	76
Molecular Characterization of a Multiethnic Group of 21 Patients with Type 3 von Willebrand Disease Giovanna Cozzi, Maria Teresa Canciani, Flora Peyvandi, Thrombosis and Haemostasis Disease EtiologyGeneticsGenetic EpidemiologyImmunologyPathology	2000	74
Molecular Characterization of PK-LR Gene in Pyruvate Kinase–Deficient Italian Patients Alberto Zanella, Paola Bianchi, Luciano Baronciani, Blood	1997	69
Rapid Purification of Glucose-6-phosphate Dehydrogenase from Mammal's Erythrocytes Paolino Ninfali, I. Orsenigo, Luciano Baronciani, Preparative Biochemistry	1990	68

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