DE LUCA G.; LEV P.; CAMACHO MF.; GOETTE NP.; SACKMAN F.; CASTRO RÍOS M.; MOIRAGUI B.; CORTES GUERRIERI V.; BENDEK G.; CARRICONDO E; ENRICO A.; VALLEJOS V.; VARELA A.; KHOURY M.; GUTIERREZ MI; LARRIPA I.; MARTA RF.; GLEMBOTSKY AC.; HELLER PG.

High cell-free DNA is associated with disease progression, inflammasome activation and elevated levels of inflammasome-related cytokine IL-18 in patients with Myelofibrosis

Frontiers in Immunology; Lugar: Bethesda; Año: 2023

GRESELE P.; FALCINELLI E; BURY L.; ALESSI MC.; GUGLIELMINI, G; FALAISE, C; PODDA, GM.; FIORE, M.; MAZZIOTA, F.; SEVIVAS, T.; BERMEJO N.; DE CANDIA E.; CHITLUR, E.; LAMBERT, MP.; BARCELLA, L.; GLEMBOTSKY, AC.; LORDKIPANIDZÉ M.

Correlation of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the BAT-LAB substudy): communication from the ISTH SSC Subcommittee on Platelet Physiology

Research and Practice in Thrombosis and Haemostasis; Año: 2023

BARONI PIETTO, M. CONSTANZA; GLEMBOTSKY AC.; LEV PR.; MARÍN OYARZÚN, CP.; DE LUCA G.; GOMEZ G.; COLLADO V.; CHARO N.; CELLUCI MS.; HELLER PG.; GOETTE NP.; MARTA RF.

Toll-like receptor expression and functional behavior in platelets from patients with systemic lupus erythematosus

IMMUNOBIOLOGY.; Año: 2023

BARONI PIETTO, M. CONSTANZA; LEV, PAOLA R.; GLEMBOTSKY, ANA C.; MARÍN OYARZÚN, CECILIA P.; GOMEZ, GRACIELA; COLLADO, VICTORIA; PISONI, CECILIA; GOMEZ, RAMIRO A.; GRODZIELSKI, MATÍAS; GONZALEZ, JACQUELINE; MARIÑO, KARINA V.; HELLER, PAULA G.; GOETTE, NORA P.; MARTA, ROSANA F.

Pathogenic mechanisms contributing to thrombocytopenia in patients with systemic lupus erythematosus

PLATELETS; Año: 2022 vol. 33 p. 743 - 754

GLEMBOTSKY, ANA C.; DE LUCA, GERALDINE; HELLER, PAULA G.

A deep dive into the pathology of gray platelet syndrome: New insights on immune dysregulation

Journal of Blood Medicine; Año: 2021 vol. 12 p. 719 - 732

GRESELE, PAOLO; FALCINELLI, EMANUELA; BURY, LOREDANA; PECCI, ALESSANDRO; ALESSI, MARIE-CHRISTINE; BORHANY, MUNIRA; HELLER, PAULA G.; SANTORO, CRISTINA; CID, ANA ROSA; ORSINI, SARA; FONTANA, PIERRE; DE CANDIA, ERICA; PODDA, GIANMARCO; KANNAN, MEGANATHAN; JURK, KERSTIN; CASTAMAN, GIANCARLO; FALAISE, CÉLINE; GUGLIELMINI, GIUSEPPE; NORIS, PATRIZIA; ZANINETTI C.; TOSSETO A.; FIORE M.; ZUÑIGA P; MIYAZAKI K; DUPUIS, A.; HAYWARD C.; CASONATTO A.; GRANDONE E.; MAZZUCONI MG.; JAMES P.; FABRIS F.; HENSKENS Y; NAPOLITANO M.; CURNOW J.; GKALEA V.; FEDOR M.; LAMBERT MP; ZIEGER B.; BARCELLA L.; COSMI B.; GIORDANO P.; PERGANTOU H; MELAZZINI F.; ABID M.; GLEMBOTSKY AC.; FERRARA G.; RUXO A.; DECKMYN H.; FRELINGER A.; HARRISON P.; MEZZANO D. ; MUMFORD AD.; LORDKIPANIDZÉ M.

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

Journal of thrombosis and haemostasis : JTH; Año: 2021 vol. 19 p. 1364 - 1371

HELLER PG.; GOETTE NP.; MARIN OYARZUN CP.; BARONI PIETTO CM.; AYALA D.; ALTUNA DR.; ARRIETA ME.; ARBESÚ G.; BASQUEIRA AL.; BONACCORSO S.; BRODSKY A.; CASTRO RÍOS M.; COSENTINI ML; DONATO H.; KORIN J.; GOMEZ S.; GUGLIELMONE H.; LAGROTTA P.; MARTI A.; NEGRO F.; RAPETTI MC.; ROSSO D.; PONZINIBBIO C.; VEBER E.; ZERGA M.; MOLINAS FC.; SAVOIA A.; PECCI A.; MARTA RF.; GLEMBOTSKY AC.

Feno-genotipificación de trombocitopenias hereditarias: nuestra experiencia en 50 familias

Revista Hematología; Año: 2020

MARÍN OYARZÚN, CECILIA P.; GLEMBOTSKY, ANA C.; GOETTE, NORA P.; LEV, PAOLA R.; DE LUCA, GERALDINE; BARONI PIETTO, MARÍA C.; MOIRAGHI, BEATRIZ; CASTRO RÍOS, MIGUEL A.; VICENTE, ANGELES; MARTA, ROSANA F.; SCHATTNER, MIRTA; HELLER, PAULA G.

Platelet Toll-Like Receptors Mediate Thromboinflammatory Responses in Patients With Essential Thrombocythemia

Frontiers in Immunology; Año: 2020 vol. 11

PACIULLO, FRANCESCO; BURY, LOREDANA; NORIS, PATRIZIA; FALCINELLI, EMANUELA; MELAZZINI, FEDERICA; ORSINI, SARA; ZANINETTI, CARLO; ABDUL-KADIR, REZAN; OBENG-TUUDAH, DEBORAH; HELLER, PAULA; GLEMBOTSKY, ANA C.; FABRIS, FABRIZIO; RIVERA, JOSE; LOZANO, MARIA LUISA; BUTTA, NORA; FAVIER, REMI; CID, ANA ROSA; FOUASSIER, MARC; PODDA, GIAN MARCO; SANTORO, CRISTINA; GRANDONE, ELVIRA; HENSKENS, YVONNE; NURDEN, PAQUITA; ZIEGER, BARBARA; CUKER, ADAM; DEVREESE, KATRIEN; TOSETTO, ALBERTO; DE CANDIA, ERICA; DUPUIS, ARNAUD; MIYAZAKI, KOJI; OTHMAN, MAHA; GRESELE, PAOLO

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

HAEMATOLOGICA; Lugar: Pavia, Italia; Año: 2020 vol. 105 p. 1948 - 1956

GRESELE, PAOLO; ORSINI, SARA; NORIS, PATRIZIA; FALCINELLI, EMANUELA; ALESSI, MARIE CHRISTINE; BURY, LOREDANA; BORHANY, MUNIRA; SANTORO, CRISTINA; GLEMBOTSKY, ANA C.; CID, ANA ROSA; TOSETTO, ALBERTO; DE CANDIA, ERICA; FONTANA, PIERRE; GUGLIELMINI, GIUSEPPE; PECCI, ALESSANDRO; HELLER, PAULA G.; RODORIGO, GIUSEPPINA; LAMMLE, BERNHARD; TRINCHERO, ALICE; PAOLO, RADOSSI; FERRARI, SILVIA; RANCITELLI, DAVIDE; STOLINSKI, AMY; ARULSELVAN, ABINAYA; LASSANDRO, GIUSEPPE

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

JOURNAL OF THROMBOSIS AND HAEMOSTASIS; Año: 2020 vol. 18 p. 732 - 739

GLEMBOTSKY ANA C.; MARIN OYARZUN CP.; DE LUCA G.; MARZAC C.; GOETTE NP.; AUGER N.; MARTA, RF.; RASLOVA H.; HELLER PG.

First description of revertant mosaicism in familial platelet disorder with predisposition to acute myelogenous leukaemia: correlation with the clinical phenotype.

HAEMATOLOGICA; Lugar: Pavia, Italia; Año: 2020

GRODZIELSKI M.; GOETTE NP.; GLEMBOTSKY AC.; BARONI C.; MENDEZ HUERGO SP.; PIERDOMINICI MS.; MONTERO VS.; RABINOVICH GA.; MOLINAS FC.; HELLER PG.; LEV PR.; MARTA RF.

Multiple concomitant mechanisms contribute to low platelet count in patients with immune thrombocytopenia.

Scientific Reports; Año: 2019

GLEMBOTSKY AC.; SILWA D.; BLUTEAU D.; BALAYN N.; MARIN OYARZUN CP.; RAINBAULT A.; BORDAS M.; DROIN N.; PIROZHKOVA I.; WASHINGTON V.; GOETTE NP.; MARTA RF.; FAVIER R.; RASLOVA H.; HELLER PG.

Downregulation of TREM-like transcript (TLT)-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.

HAEMATOLOGICA; Lugar: Pavia, Italia; Año: 2019

DE ROCCO D.; MELAZZINI F.; MARCONI C.; PECCI A.; BOTTEGA R; PALOMBO F.; GIORDANO P; COCCIOLI M; GLEMBOTSKY AC; HELLER PG.; SERI M.; SAVOIA A.; NORIS P.

Mutations of RUNX1 in families with inherited thrombocytopenia.

AMERICAN JOURNAL OF HEMATOLOGY; Lugar: New York; Año: 2017

ORSINI S; NORIS P.; BURY L.; HELLER PG.; SANTORO C.; KADIR RA; BUTTA NC; FALCINELLI E; CID AR.; FABRIS F.; FOUASSIER M; MIYAZAKI K; LOZANO ML; ZUÑIGA P; FLAUJAC C; PODDA GM.; BERMEJO N.; FAVIER R.; HENSKENS Y; DE MAISTRE E; DE CANDIA E.; MUMFORD AD; OZDEMIR NG; EKER I; NURDEN P.; BAYART S; LAMBERT MP; BUSSEL J.; ZIEGER B; TOSSETO A.; MELAZZINI F.; GLEMBOTSKY AC.; PECCI A.; CATTANEO M; SCHLEGEL N.; GRESELE P.

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders. The Surgery in Platelet disorders And Therapeutic Approach (SPATA) study.

HAEMATOLOGICA; Lugar: Pavia, Italia; Año: 2017

BOTTEGA R; NICCHIA E; ALFANO C.; GLEMBOTSKY AC.; PASTORE A.; BERTAGGIA-CALDERARA D; BISIG B; DUCHOSAL MA; ARBESÚ G; ALBERIO L; HELLER PG.; SAVOIA A.

Gray platelet syndrome: Novel mutations of the NBEAL2 gene.

AMERICAN JOURNAL OF HEMATOLOGY; Lugar: New York; Año: 2017

SALIM JP.*; GLEMBOTSKY AC.*; LEV PR.; MARIN OYARZUN CP.; GOETTE NP.; MOLINAS FC.; MARTA RF.; HELLER PG.

Differential expression of SDF-1 receptor CXCR4 in molecularly defined forms of inherited thrombocytopenias

PLATELETS; Lugar: Londres; Año: 2017

DI BUDUO, CA; ALBERELLI MA; GLEMBOTSKY AC.; PODDA GM.; LEV PR.; CATTANEO M; LANDOLFI R; HELLER PG.; BALDUINI A.; DE CANDIA E.

Abnormal proplatelet formation and emperipolesis in cultured human megakaryocytes from gray platelet syndrome patients.

Scientific Reports; Año: 2016

GOETTE NP.; GLEMBOTSKY AC.; LEV PR.; GRODZIELSKI M.; CONTRUFO G.; PIERDOMINICI MS.; ESPASANDIN YR.; RIVEROS D.; GARCIA A.; MOLINAS FC.; HELLER PG.; MARTA RF.

Platelet Apoptosis in Adult Immune Thrombocytopenia: Insights into the Mechanism of Damage Triggered by Auto-antibodies

PLOS ONE; Lugar: San Francisco; Año: 2016

MARIN OYARZUN CP.; CARESTIA A; LEV PR.; GLEMBOTSKY AC.; CASTRO RÍOS M.; MOIRAGUI B.; MOLINAS FC.; MARTA RF.; SCHATTNER M.; HELLER PG.

Neutrophil extracellular trap formation and circulating nucleosomes in patients with chronic myeloproliferative neoplasms

Scientific Reports; Año: 2016

MELA OSORIO MJ; FERRARI L.; GOETTE NP.; GUTIERREZ MI; GLEMBOTSKY AC.; MALDONADO AC; LEV PR.; ALVAREZ C.; KORIN L.; MARTA RF.; MOLINAS FC.; HELLER PG.

Long-term follow-up of essential thrombocythemia patients treated with anagrelide: subgroup analysis according to JAK2/CALR/MPL mutational status.

EUROPEAN JOURNAL OF HAEMATOLOGY; Lugar: Londres; Año: 2015

ESPASANDIN YR.; GLEMBOTSKY AC.; GRODZIELSKI M.; LEV PR.; GOETTE NP.; MOLINAS FC.; MARTA RF.; HELLER PG.

Anagrelide platelet-lowering effect is due to inhibition of both megakaryocyte maturation and proplatelet formation: insight into potential mechanisms.

JOURNAL OF THROMBOSIS AND HAEMOSTASIS; Lugar: Londres; Año: 2015 vol. 13 p. 631 - 642

LARROCA LM.; HELLER PG.; PODDA GM.; PUJOL-MOIX N.; GLEMBOTSKY AC.; PECCI A.; ALBERELLI MA; BALDUINI CL.; LANDOLFI R; CATTANEO M; DE CANDIA E.

Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndrome.

PLATELETS; Lugar: Londres; Año: 2015 p. 1 - 7

MELA OSORIO MJ; FERRARI L.; GOETTE NP.; GUTIERREZ MI; GLEMBOTSKY AC.; MALDONADO AC; LEV PR.; ALVAREZ C.; KORIN L.; MARTA RF.; MOLINAS FC.; HELLER PG.

Long-term follow-up of essential thrombocythemia patients treated with anagrelide: subgroup analysis according to JAK2/CALR/MPL mutational status

European Journal of Haematology; Año: 2015

LEV PR.; GRODZIELSKI M.; GOETTE NP.; GLEMBOTSKY AC.; ESPASANDIN YR.; PIERDOMINICI MS.; CONTRUFO G.; MONTERO V.; FERRARI L.; MOLINAS FC.; HELLER PG.; MARTA RF.

Impaired proplatelet formation in immune thrombocytopenia: a novel mechanism contributing to decreased platelet count.

BRITISH JOURNAL OF HAEMATOLOGY; Lugar: Londres; Año: 2014 vol. 165 p. 854 - 864

NORIS P.; SCHLEGEL N.; KLERSY C.; HELLER PG.; CIVASCHI E.; PUJOL-MOIX N.; FABRIS F.; FAVIER R.; GRESELE P.; LATGER-CANNARD V.; CUKER A.; NURDEN P.; GREINACHER A.; CATTANEO M; DE CANDIA E.; PECCI A.; HURTAUD-ROUX MF.; GLEMBOTSKY AC.; MUÑIZ-DIAZ E.; RANDI ML..; TRILLOT N.; BURY L.; LECOMPTE T.; MARCONI C.; SAVOIA A.; BALDUINI CL.

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

HAEMATOLOGICA; Lugar: Pavia, Italia; Año: 2014 vol. 99 p. 1387 - 1394

PECCI A.; KLERSY C.; GRESELE P.; LEE KJ; DE ROCCO D.; BOSSI V.; RUSSO G.; HELLER PG.; LOFFREDO G; BALLMAIER M.; FABRIS F.; BEGGIATO E.; KAHR WH.; PUJOL-MOIX N.; PLATOKOUKI H.; VAN GEET C.; NORIS P.; YERRAM P.; HERMANS C.; GERBER B.; ECONOMOU M.; DE GROOT M.; ZIEGER B.; DE CANDIA E.; FRATICELLI V.; KERSSEBOOM R.; PICCOLI GB.; ZIMMERMANN S.; FIERRO T.; GLEMBOTSKY AC.; VIANELLO F.; ZANINETTI C.; NICCHIA E; GÜTHNER C.; BARONCI C.; SERI M.; KNIGHT PJ; BALDUINI CL.; SAVOIA A.

MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations

HUMAN MUTATION; Lugar: New York; Año: 2014 vol. 35 p. 236 - 247

GLEMBOTSKY AC.; BLUTEAU D.; ESPASANDIN YR.; GOETTE NP.; MARTA RF.; MARIN OYARZUN CP.; KORIN L.; LEV PR; LAGUENS RP.; MOLINAS FC.; RASLOVA H.; HELLER PG.

Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets.

Journal of Thrombosis and Haemostasis; Año: 2014 vol. 12 p. 761 - 772

BOTTEGA R; PECCI A.; DE CANDIA E.; PUJOL-MOIX N; HELLER PG.; NORIS P; DE ROCCO D.; PODDA GM; GLEMBOTSKY AC.; CATTANEO M; BALDUINI CL; SAVOIA A.

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

HAEMATOLOGICA; Lugar: Pavia, Italia; Año: 2013 vol. 98 p. 868 - 874

DE ROCCO D.; ZIEGER B; PLATOKOUKI H; HELLER PG.; PASTORE A.; BOTTEGA R; NORIS P; BAROZZI S; GLEMBOTSKY AC.; PERGANTOU H; BALDUINI CL.; SAVOIA A.; PECCI A.

MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations.

EUROPEAN JOURNAL OF MEDICAL GENETICS; Lugar: Amsterdam; Año: 2013 vol. 56 p. 7 - 12

GLEMBOTSKY AC; MARTA RF.; PECCI A.; DE ROCCO D.; GNAN C.; ESPASANDIN YR.; GOETTE NP.; NEGRO F; NORIS P; SAVOIA A.; BALDUINI CL.; MOLINAS FC.; HELLER PG.

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

JOURNAL OF THROMBOSIS AND HAEMOSTASIS; Lugar: Londres; Año: 2012 vol. 10 p. 1653 - 1661

BLUTEAU D.; GLEMBOTSKY AC.; RAINBAULT A.; BALAYN N.; GILLES L.; RAMEAU P.; NURDEN P.; ALESSI MC.; DEBILI N.; VAINCHENKER W.; HELLER PG.; FAVIER R.; RASLOVA H.

Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression.

BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY - PRINT; Lugar: Washington; Año: 2012 p. 2708 - 2718

LEV PR; GOETTE NP.; GLEMBOTSKY AC; LAGUENS RP.; CABEZA MECKERT PM.; SALIM JP.; HELLER PG; POZNER RG.; MARTA RF; MOLINAS FC.

Production of functional platelet-like particles by the megakaryoblastic DAMI cell line provides a model for platelet biogenesis

PLATELETS; Lugar: Londres; Año: 2011 p. 26 - 36

GLEMBOTSKY AC.; KORIN L.; LEV PR.; CHAZARRETA CD.; MARTA RF.; MOLINAS FC.; HELLER PG.

Screening for MPL mutations in essential thrombocythemia and primary myelofibrosis: normal Mpl expression and absence of constitutive STAT3 and STAT5 activation in MPLW515L-positive platelets.

EUROPEAN JOURNAL OF HAEMATOLOGY; Lugar: Londres; Año: 2010 vol. 84 p. 398 - 405

GOETTE NP.; LEV PR.; HELLER PG.; GLEMBOTSKY AC.; CHAZARRETA CD.; SALIM JP.; MOLINAS FC.; MARTA RF.

Abnormal regulation of soluble and anchored IL-6 receptor in monocytes from patients with essential thrombocythemia

EXPERIMENTAL HEMATOLOGY; Año: 2010 p. 868 - 876

DE ROCCO D.; HELLER PG.; GIROTTO G.; PASTORE A.; GLEMBOTSKY AC.; MARTA RF.; BOZZI V.; PECCI A.; MOLINAS FC.; SAVOIA A.

MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 gene.

PLATELETS; Lugar: Londres; Año: 2009 vol. 20 p. 598 - 602

HELLER PG.; GLEMBOTSKY AC.; GOETTE NP.; MARTA RF.; LEV PR,.; MOLINAS FC.

Diverse Mpl expression pattern among pedigrees with inherited thrombocytopenia: potential diagnostic and therapeutic implications.

Journal of Thrombosis and Haemostasis; Lugar: England; Año: 2008 p. 2215 - 2217

HELLER PG; LEV PR; SALIM JP; KORNBLIHTT LI; GOETTE NP.; CHAZARRETA CD; GLEMBOTSKY AC; VASALLU PS; MARTA RF; MOLINAS FC

JAK2V617F mutation in platelets from essential thrombocythemia patients: correlation with clinical features and analysis of STAT5 phosphorylation status

European Journal of Haematology; Año: 2006 vol. 77 p. 210 - 216

HELLER PG; PECCI A; GLEMBOTSKY AC; SAVOIA A; NEGRO F; BALDUINI CL; MOLINAS FC

Unexplained recurrent venous thrombosis in a patient with MYH9-related disease.

PLATELETS; Año: 2006 p. 274 - 275

HELLER PG.; GLEMBOTSKY AC.; GANDHI M.; CUMMINGS C.; PIROLA C.; MARTA RF.; KORNBLIHTT LI; DRACHMAN J.; MOLINAS FC.

Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia an a novel AML1 mutation.

BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY - PRINT; Lugar: Washington; Año: 2005 vol. 105 p. 4664 - 4670

MARTA RF; GOETTE NP.; LEV PR; HELLER PG; KORNBLIHTT LI; VASSALLU PS; GLEMBOTSKY AC; PIROLA C; MOLINAS F.

Increased plasmatic IL-6 soluble receptor in patients with essential thrombocythemia.

HAEMATOLOGICA; Año: 2004 p. 657 - 663