P. Noris

发表

Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation.

D. Bluteau, A. Balduini, N. Balayn, 2014, The Journal of clinical investigation.

Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis

V. Poggi, P. Noris, A. Savoia, 2003, Thrombosis and Haemostasis.

Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations.

A. Balduini, P. Noris, A. Savoia, 2005, Human molecular genetics.

Innovation in the field of thrombocytopenias: achievements since the beginning of the century and promises for the future

P. Noris, C. Balduini, 2016, Haematologica.

Reversal of Thrombin-Induced Deactivation of CD39/ATPDase in Endothelial Cells by HMG-CoA Reductase Inhibition: Effects on Rho-GTPase and Adenosine Nucleotide Metabolism

P. Noris, G. Ricevuti, C. Balduini, 2002, Arteriosclerosis, thrombosis, and vascular biology.

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

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

Impact of COVID-19 on liver function: results from an internal medicine unit in Northern Italy

F. Baldanti, G. Corazza, G. Freddi, 2020, Internal and Emergency Medicine.

Laboratory monitoring of P2Y12 inhibitors: communication from the SSC of the ISTH

P. Noris, A. L. Frelinger, C. Gachet, 2018, Journal of thrombosis and haemostasis : JTH.

Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia

Christopher C. Porter, Michael Doubek, Kenneth Jones, 2015, Nature Genetics.

Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency

P. Noris, A. Savoia, C. Balduini, 2013, Haematologica.

Spectrum of the Mutations in Bernard–Soulier Syndrome

A. Pastore, P. Noris, R. Favier, 2014, Human mutation.

Max(a), a new low-frequency platelet-specific antigen localized on glycoprotein IIb, is associated with neonatal alloimmune thrombocytopenia.

P. Noris, C. E. van der Schoot, A. von dem Borne, 1995, Blood.

Clinical management, ethics and informed consent related to multi‐gene panel‐based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH

K. Downes, P. Noris, A. Greinacher, 2020, Journal of thrombosis and haemostasis : JTH.

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

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

M. Ballmaier, P. Noris, P. Knight, 2014, Human mutation.

ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia

A. Pastore, P. Noris, T. Pippucci, 2018, British journal of haematology.

A NEW FORM OF INHERITED THROMBOCYTOPENIA CAUSED BY LOSS-OF-FUNCTION MUTATIONS IN PTPRJ

A. Balduini, P. Noris, N. Katsanis, 2018 .

Platelet count and aging

P. Noris, C. Balduini, 2014, Haematologica.

Platelet Counting and Measurement of Platelet Dimensions

P. Noris, C. Zaninetti, 2017 .

New roles for mean platelet volume measurement in the clinical practice?

P. Noris, C. Balduini, F. Melazzini, 2016, Platelets.

Safety and efficacy of low‐dose fondaparinux (1.5 mg) for the prevention of venous thromboembolism in acutely ill medical patients with renal impairment: the FONDAIR study

W. Ageno, F. Dentali, P. Noris, 2012, Journal of thrombosis and haemostasis : JTH.

Platelet composition and function in patients undergoing cardiopulmonary bypass for heart surgery.

P. Noris, G. Mazzini, P. Ceriana, 1996, Haematologica.

Activation of the hemostatic process in patients with unruptured aortic aneurysm before and in the first week after surgical repair.

P. Noris, G. Gamba, N. Montani, 1997, Haematologica.

Effect of different sample preparation methods on the results of the impedance technique in the study of platelet hyper- and hypo-function in whole blood.

P. Noris, C. Balduini, G. Bertolino, 1993, Thrombosis research.

Platelet aggregation in platelet-rich plasma and whole blood in 120 patients with myeloproliferative disorders.

P. Noris, C. Balduini, G. Bertolino, 1991, American journal of clinical pathology.

Platelet aggregation in platelet rich plasma and whole blood in 18 patients affected by idiopathic myelofibrosis *

P. Noris, E. Ascari, G. Barosi, 1988, European journal of haematology.

The effect of red cells on platelet aggregation: a study with the electronic whole blood aggregometer.

P. Noris, E. Ascari, C. Balduini, 1988, Scandinavian journal of clinical and laboratory investigation.

Transfusion of platelet concentrates cryopreserved with ThromboSol plus low‐dose dimethylsulphoxide in patients with severe thrombocytopenia: a pilot study

P. Noris, P. Pedrazzoli, R. Schiavo, 2000, British journal of haematology.

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.

Mean platelet volume for distinguishing between inherited thrombocytopenias and immune thrombocytopenia – response to Beyan

P. Noris, C. Balduini, 2013, British journal of haematology.

Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: An EHA Consensus Report

P. Noris, A. Srivastava, V. Blanchette, 2019, HemaSphere.

Platelet function after in vivo and in vitro treatment with thrombolytic agents.

P. Noris, M. Previtali, C. Balduini, 1992, The American journal of cardiology.

Thrombopoietin levels in patients with primary and reactive thrombocytosis

P. Noris, C. Balduini, A. Cerutti, 1997, British journal of haematology.

Autologous Platelet Collection and Storage to Support Thrombocytopenia in Patients Undergoing High-Dose Chemotherapy and Circulating Progenitor Cell Transplantation for High-Risk Breast Cancer

P. Noris, P. Pedrazzoli, A. Livraghi, 1998, Vox Sanguinis.

Autologous platelet transfusion in patients receiving high-dose chemotherapy and circulating progenitor cell transplantation for stage II/III breast cancer.

P. Noris, P. Pedrazzoli, M. Battaglia, 1998, Haematologica.

Cryopreservation of human platelets using dimethyl sulfoxide and glycerol-glucose: effects on "in vitro" platelet function.

P. Noris, F. Sinigaglia, L. Salvaneschi, 1993, Haematologica.

Acquired cyclic thrombocytopenia‐thrombocytosis with periodic defect of platelet function

P. Noris, E. Ascari, V. Rosti, 1993, British journal of haematology.

A review of platelet secretion assays for the diagnosis of inherited platelet secretion disorders

P. Noris, C. Gachet, A. Frelinger, 2015, Thrombosis and Haemostasis.

Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial

P. Noris, A. Bertomoro, F. Fabris, 2019, Haematologica.

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.

P. Noris, A. Savoia, C. Klersy, 2010, Blood.

Particulate cytoplasmic structures with high concentration of ubiquitin-proteasome accumulate in myeloid neoplasms

P. Noris, E. Solcia, A. Pecci, 2015, Journal of Hematology & Oncology.

Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation

P. Noris, A. Savoia, M. Morel-Kopp, 2021, Haematologica.

Dominant inheritance of a novel integrin β3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families

P. Noris, L. Cecchetti, A. Savoia, 2009, Haematologica.

Investigational drugs in thrombotic thrombocytopenic purpura

P. Noris, C. Balduini, 2011, Expert opinion on investigational drugs.

High versus standard dose methylprednisolone in the acute phase of idiopathic thrombotic thrombocytopenic purpura: a randomized study

P. Galieni, P. Noris, E. Ascari, 2010, Annals of Hematology.

Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome).

R. Ravazzolo, P. Noris, G. Ghiggeri, 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome

P. Noris, F. Fabris, A. Savoia, 2012, PloS one.

Altered cytoskeleton organization in platelets from patients with MYH9‐related disease

A. Balduini, P. Noris, A. Pecci, 2005, Journal of thrombosis and haemostasis : JTH.

Immunocytochemistry for the heavy chain of the non‐muscle myosin IIA as a diagnostic tool for MYH9‐related disorders

P. Noris, G. Ghiggeri, A. Savoia, 2002, British journal of haematology.

Defective expression of GPIb/IX/V complex in platelets from patients with May-Hegglin anomaly and Sebastian syndrome.

P. Noris, A. Savoia, C. Balduini, 2002, Haematologica.

International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country

P. Noris, A. Savoia, C. Balduini, 2012, Journal of thrombosis and haemostasis : JTH.

Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

P. Noris, F. Fabris, A. Savoia, 2010, Thrombosis and Haemostasis.

von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets

P. Noris, A. Federici, C. Balduini, 2006, Platelets.

Design and methods

M. Marcelli, G. Karsenty, J. Estrade, 2016 .

Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation

P. Noris, F. Locatelli, C. Klersy, 2001, Leukemia.

In vitro and in vivo effects of desmopressin on platelet function.

P. Noris, C. Balduini, G. Gamba, 1999, Haematologica.

A new variant of Bernard‐Soulier syndrome characterized by dysfunctional glycoprotein (GP) Ib and severely reduced amounts of GPIX and GPV

E. Arbustini, P. Noris, C. Balduini, 1998, British journal of haematology.

Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly): clinical and laboratory findings.

P. Noris, C. Balduini, U. Magrini, 1998, The American journal of medicine.

A phenylalanine‐55 to serine amino‐acid substitution in the human glycoprotein IX leucine‐rich repeat is associated with Bernard‐Soulier syndrome

P. Noris, J. Stibbe, S. Simsek, 1997, British journal of haematology.

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome.

P. Noris, S. Perrotta, A. Savoia, 2001, Blood.

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

P. Nurden, P. Noris, R. Favier, 2017, Haematologica.

Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study

P. Nurden, P. Noris, R. Favier, 2019, Haematologica.

GP1BB c.179C > T is the most frequent cause of monoallelic Bernard–Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families

P. Noris, A. Savoia, A. Pecci, 2022, Annals of Hematology.

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.

Cys209 Ser mutation in the platelet membrane glycoprotein ibα gene is associated with Bernard‐Soulier syndrome

A. Borne, P. Noris, A. Ribera, 1994, British journal of haematology.

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

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

In vitro platelet aggregation defects in patients with myeloproliferative disorders and high platelet counts: Are they laboratory artefacts?

C. Tinelli, P. Noris, G. Barosi, 2009, Platelets.

Marco Seri, Tommaso Pippucci, Anna Savoia, 2015, Blood.

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.

U Magrini, R. Ravazzolo, P. Noris, 2000, Nature genetics.

P. Noris, A. Savoia, S. Ryhänen, 2018, Hämostaseologie.

Diagnosis and Management of Inherited Thrombocytopenias

P. Noris, C. Balduini, A. Pecci, 2013, Seminars in Thrombosis & Hemostasis.

A. Pastore, P. Noris, A. Savoia, 2013, European journal of medical genetics.

Inherited thrombocytopenias

P. Noris, C. Balduini, A. Pecci, 2012, Hämostaseologie.

R. Ravazzolo, P. Noris, P. Koivisto, 2003, Medicine.

Position of nonmuscle myosin heavy chain IIA (NMMHC‐IIA) mutations predicts the natural history of MYH9‐related disease

P. Noris, P. Koivisto, F. Fabris, 2008, Human mutation.

Expert opinion on the use of platelet secretion assay for the diagnosis of inherited platelet function disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology

P. Noris, M. Lordkipanidzé, A. Mumford, 2022, Journal of thrombosis and haemostasis : JTH.

Ristocetin-induced Platelet Agglutination Stimulates GPIIb/IIIa-dependent Calcium Influx

P. Noris, C. Balduini, C. Balduini, 1995, Thrombosis and Haemostasis.

Inherited thrombocytopenias in the era of personalized medicine

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

Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia

P. Noris, F. Passamonti, F. Locatelli, 2009, Journal of thrombosis and haemostasis : JTH.

Hereditary thrombocytopenias: a growing list of disorders.

P. Noris, A. Pecci, 2017, Hematology. American Society of Hematology. Education Program.

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.

Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.

P. Noris, S. Perrotta, T. Pippucci, 2011, American journal of human genetics.

P. Noris, N. Vianelli, L. Catani, 2015, British journal of haematology.

Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations

P. Noris, A. Savoia, M. Di Stazio, 2007, Haematologica.

Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia.

A. Balduini, P. Noris, N. Katsanis, 2019, Blood.

Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia

A. Balduini, P. Noris, T. Pippucci, 2016, Haematologica.

Clinical and pathogenetic features of ETV6 related thrombocytopenia with predisposition to acute lymphoblastic leukemia

A. Balduini, P. Noris, T. Pippucci, 2016 .

Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombocytopenia

A. Balduini, P. Noris, E. Solcia, 2012, Thrombosis and Haemostasis.

Proplatelet formation in heterozygous Bernard‐Soulier syndrome type Bolzano

A. Balduini, P. Noris, C. Balduini, 2009, Journal of thrombosis and haemostasis : JTH.

Incompatibility for CD31 and human platelet antigens and acute graft‐versus‐host disease after bone marrow transplantation

P. Noris, F. Locatelli, C. Klersy, 1999, British journal of haematology.

Prescribing and dispensing data sources in New Zealand: their usage and future directions

P. Noris, G. Becket, P. Herbison, 2009 .

A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene

P. Noris, T. Pippucci, A. Savoia, 2018, British journal of haematology.

Mutations of RUNX1 in families with inherited thrombocytopenia

P. Noris, A. Savoia, P. Giordano, 2017, American journal of hematology.

A. Balduini, P. Noris, T. Pippucci, 2016, Thrombosis and Haemostasis.

Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy

R. Bruno, F. Baldanti, R. Maserati, 2020, Internal and Emergency Medicine.

Effect of endothelial cells on platelet aggregation in platelet rich plasma (PRP) and whole blood.

P. Noris, F. Piovella, C. Balduini, 1990, Thrombosis research.

Thrombopoietin is not uniquely responsible for thrombocytosis in inflammatory disorders

P. Noris, C. Balduini, A. Pecci, 2007, Platelets.

A. Pastore, P. Noris, M. La Bianca, 2021, Haematologica.

Megakaryocytes derived from patients with the classical form of Bernard-Soulier syndrome show no ability to extend proplatelets in vitro

A. Balduini, P. Noris, C. Balduini, 2011, Platelets.

Defect of Platelet Aggregation and Adhesion Induced by Autoantibodies Against Platelet Glycoprotein IIIa

P. Noris, G. Mazzini, F. Sinigaglia, 1992, Thrombosis and Haemostasis.

Interrelation of platelet aggregation, release reaction and thromboxane A2 production.

P. Noris, F. Sinigaglia, C. Balduini, 1988, Biochemical and biophysical research communications.

Donor–recipient incompatibility at CD31‐codon 563 is a major risk factor for acute graft‐versus‐host disease after allogeneic bone marrow transplantation from a human leucocyte antigen‐matched donor

P. Noris, F. Locatelli, C. Klersy, 2001, British journal of haematology.

A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly

P. Noris, A. Savoia, A. Pecci, 2021, International journal of molecular sciences.

Autosomal dominant thrombocytopenias with reduced expression of glycoprotein Ia

P. Noris, A. Savoia, C. Balduini, 2006, Thrombosis and Haemostasis.

Effect of anagrelide on platelet count and function in patients with thrombocytosis and myeloproliferative disorders.

P. Noris, E. Ascari, C. Balduini, 1992, Haematologica.

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

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

Anemia in patients with Covid-19: pathogenesis and clinical significance

G. Freddi, P. Noris, U. Sabatini, 2021, Clinical and Experimental Medicine.

Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC

P. Noris, A. Tosetto, P. Fontana, 2019, Journal of thrombosis and haemostasis : JTH.

Heparin infusion facilitates ex vivo spontaneous platelet aggregation in patients with acute myocardial infarction who have undergone thrombolytic therapy.

P. Noris, M. Previtali, M. Ferrario, 1993, Haemostasis.

Platelet-Independent defect in hemostasis associated with sirolimus use.

P. Noris, M. Marasà, A. Dal Canton, 2004, Transplantation proceedings.

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.

Hemophagocytic syndrome responding to high-dose gammaglobulin as presenting feature of sarcoidosis.

P. Noris, C. Balduini, C. Loni, 1997, American journal of hematology.

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.

The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology

P. Noris, M. Alessi, P. Fontana, 2021, Journal of thrombosis and haemostasis : JTH.

Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup

P. Noris, T. Pippucci, A. Savoia, 2022, Haematologica.

P. Noris, A. Savoia, Valeria Capaci, 2022, Haematologica.

Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris‐Trousseau type

P. Noris, R. Valli, L. Mare, 2012, European journal of haematology.

Inherited thrombocytopenias

P. Noris, C. Balduini, A. Pecci, 2012, Hämostaseologie.

A Type of Heterozygous Bernard-soulier Syndrome Autosomal Dominant Macrothrombocytopenia in Italy Is Most Frequently

V. Poggi, P. Noris, S. Perrotta, 2022 .

Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients.

P. Noris, A. Savoia, M. Di Stazio, 2004, Haematologica.

Peripheral arteriopathy of the lower limbs in a patient with severe congenital thrombocytopenia

P. Noris, G. Gensini, D. Poli, 2006, Internal and emergency medicine.

Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: A EHA Consensus Report

P. Noris, A. Tosetto, F. Leebeek, 2019 .

Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin

P. Noris, S. Perrotta, A. Savoia, 2009, Platelets.

A review of platelet secretion assays for the diagnosis of inherited platelet secretion disorders

P. Noris, C. Gachet, A. Mumford, 2015, Thrombosis and Haemostasis.

Spectrum of the Mutations in Bernard–Soulier Syndrome

A. Pastore, P. Noris, R. Favier, 2014, Human mutation.

Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC

P. Noris, A. Tosetto, P. Fontana, 2019, Journal of thrombosis and haemostasis : JTH.

A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene

P. Noris, T. Pippucci, A. Savoia, 2018, British journal of haematology.

International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country

P. Noris, A. Savoia, C. Balduini, 2012, Journal of thrombosis and haemostasis : JTH.

Heparin Modifies Platelet Count and Function in Patients who Have Undergone Thrombolytic Therapy for Acute Myocardial Infarction

P. Noris, C. Balduini, Giampiera Bertolino, 1993, Thrombosis and Haemostasis.

Relationship between size and thiazole orange fluorescence of platelets in patients undergoing high‐dose chemotherapy

P. Noris, P. Spedini, Balduini, 1999, British journal of haematology.

A. Pastore, P. Noris, A. Savoia, 2013, European journal of medical genetics.

Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia.

A. Balduini, P. Noris, N. Katsanis, 2019, Blood.

Small red blood cells mimicking platelets.

P. Noris, C. Balduini, 2014, Blood.