E. Civaschi

发表

Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

A. Pastore, P. Noris, A. Savoia, 2011, Haematologica.

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.

P. Noris, F. Fabris, A. Savoia, 2014, Blood.

Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study

P. Noris, C. Klersy, P. Gresele, 2013, British journal of haematology.

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)

P. Noris, S. Perrotta, A. Savoia, 2012, Haematologica.

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

P. Nurden, P. Noris, R. Favier, 2014, Haematologica.

ANKRD26-related thrombocytopenia and myeloid malignancies.

Paola Giordano, Marco Seri, Anna Savoia, 2013, Blood.

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.

P. Noris, S. Perrotta, T. Pippucci, 2011, Blood.

Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia

P. Noris, G. Biino, C. Balduini, 2015, Haematologica.

Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders

P. Nurden, P. Noris, R. Favier, 2015, British journal of haematology.

β‐1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia

P. Noris, P. Giannakakou, J. Bussel, 2015, Journal of thrombosis and haemostasis : JTH.