BARONI PIETTO, MARÍA C.; GLEMBOTSKY, ANA C.; LEV, PAOLA R.; MARÍN OYARZÚN, CECILIA R.; DE LUCA, GERALDINE; GOMEZ, GRACIELA; COLLADO, MARÍA V.; CHARÓ, NANCY; CELLUCCI, ADELA S.; HELLER, PAULA G.; GOETTE, NORA P.; MARTA, ROSANA F.

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

IMMUNOBIOLOGY.; Año: 2024 vol. 229

DE LUCA, GERALDINE; LEV, PAOLA R.; CAMACHO, MARIA F.; GOETTE, NORA P.; SACKMANN, FEDERICO; CASTRO RÍOS, MIGUEL A.; MOIRAGHI, BEATRIZ; CORTES GUERRIERI, VERONICA; BENDEK, GEORGINA; CARRICONDO, EMILIANO; ENRICO, ALICIA; VALLEJO, VERONICA; VARELA, ANA; KHOURY, MARINA; GUTIERREZ, MARINA; LARRIPA, IRENE B.; MARTA, ROSANA F.; GLEMBOTSKY, ANA C.; HELLER, PAULA G.

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; Año: 2023 vol. 14

GOETTE, NORA P.; BORZONE, FRANCISCO R.; DISCIANNI LUPI, AILEN D.; CHASSEING, NORMA A.; RUBIO, MARÍA F.; COSTAS, MÓNICA A.; HELLER, PAULA G.; MARTA, ROSANA F.; LEV, PAOLA R.

Megakaryocyte–stromal cell interactions: Effect on megakaryocyte proliferation, proplatelet production, and survival

EXPERIMENTAL HEMATOLOGY; Año: 2022

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

ROSS, JUSTYNE E.; ZHANG, BING M.; LEE, KRISTY; MOHAN, SHRUTHI; BRANCHFORD, BRIAN R.; BRAY, PAUL; DUGAN, STEFANIE N.; FRESON, KATHLEEN; HELLER, PAULA G.; KAHR, WALTER H.A.; LAMBERT, MICHELE P.; LUCHTMAN-JONES, LORI; LUO, MINJIE; BOTERO, JULIANA PEREZ; RONDINA, MATTHEW T.; RYAN, GABRIELLA; WESTBURY, SARAH; BERGMEIER, WOLFGANG; DI PAOLA, JORGE

Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel

Blood Advances; Año: 2021 vol. 5 p. 414 - 431

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, CARLO; FIORE, MATHIEU; TOSETTO, ALBERTO; ZUNIGA, PAMELA; MIYAZAKI, KOJI; DUPUIS, ARNAUD; HAYWARD, CATHERINE; CASONATO, ALESSANDRA; GRANDONE, ELVIRA; MAZZUCCONI, MARIA GABRIELLA; JAMES, PAULA; FABRIS, FABRIZIO; HENSKENS, YVONNE; NAPOLITANO, MARIASANTA; CURNOW, JENNIFER; GKALEA, VASILIKI; FEDOR, MARIAN; LAMBERT, MICHELE P.; ZIEGER, BARBARA; BARCELLA, LUCA; COSMI, BENILDE; GIORDANO, PAOLA; PORRI, CLAUDIA; MELAZZINI, FEDERICA; ABID, MADIHA; GLEMBOTSKY, ANA C.; FERRARA, GRAZIA; RUSSO, ALEXANDRA; DECKMYN, HANS; FRELINGER, ANDREW L.; HARRISON, PAUL; MEZZANO, DIEGO; MUMFORD, ANDREW D; LORDKIPANIDZÉ, MARIE

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; Año: 2021 vol. 19 p. 1364 - 1371

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

GLEMBOTSKY AC; MARIN OYARZUN CP; DE LUCA G; MARZAC C; AUGER N; GOETTE NP; 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 vol. 105 p. 535 - 539

ODSTRCIL-BOBILLO MS; KOHAN D; HELLER PG; OTERO V; RUSSO MP; BASQUIERA AL

Ileitis as presentation of lymphoma in Wiskott-Aldrich syndrome.

MEDICINA (BUENOS AIRES); Lugar: Buenos Aires; Año: 2020 vol. 80 p. 81 - 83

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

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; LUCEROS, ANALIA SANCHEZ; JANDROT?PERRUS, MARTINE; KUNISHIMA, SHINJI; RIVERA POZO, JOSÉ; LORDKIPANIDZÉ, MARIE; MELAZZINI, FEDERICA; FALAISE, CÉLINE; CASONATO, ALESSANDRA; PODDA, GIANMARCO; KANNAN, MEGANATHAN; JURK, KERSTIN; SEVIVAS, TERESA; CASTAMAN, GIANCARLO; GRANDONE, ELVIRA; FIORE, MATHIEU; ZUNIGA, PAMELA; HENSKENS, YVONNE; MIYAZAKI, KOJI; DUPUIS, ARNAUD; HAYWARD, CATHERINE; ZANINETTI, CARLO; ABID, MADIHA; FERRARA, GRAZIA; MAZZUCCONI, MARIA GABRIELLA; TAGARIELLO, GIUSEPPE; JAMES, PAULA; FABRIS, FABRIZIO; RUSSO, ALEXANDRA; BERMEJO, NURIA; NAPOLITANO, MA

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.; SLIWA, DOMINIKA; BLUTEAU, DOMINIQUE; BALAYN, NATHALIE; OYARZÚN, CECILIA P. MARIN; RAIMBAULT, ANNA; BORDAS, MARIE; DROIN, NATHALIE; PIROZHKOVA, IRYNA; WASHINGTON, VALANCE; GOETTE, NORA P.; MARTA, ROSANA F.; FAVIER, RÉMI; RASLOVA, HANA; HELLER, PAULA G.

Downregulation of TREM-like transcript-1 and collagen receptor alpha;2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia

HAEMATOLOGICA; Año: 2019 vol. 104 p. 1244 - 1255

D'ATRI, LINA PAOLA; RODRÍGUEZ, CAMILA SOFÍA; MIGUEL, CAROLINA PAULA; POZNER, ROBERTO GABRIEL; ORTIZ WILCZYÑSKI, JUAN MANUEL; NEGROTTO, SOLEDAD; CARRERA-SILVA, EUGENIO ANTONIO; HELLER, PAULA GRACIELA; SCHATTNER, MIRTA

Activation of toll‐like receptors 2 and 4 on CD 34 + cells increases human megakaryo/thrombopoiesis induced by thrombopoietin

JOURNAL OF THROMBOSIS AND HAEMOSTASIS; Año: 2019

MARIN OYARZÚN, CECILIA P.; HELLER, PAULA G.

Platelets as mediators of thromboinflammation in chronic myeloproliferative neoplasms

Frontiers in Immunology; Año: 2019 vol. 10

GRODZIELSKI, MATÍAS; GOETTE, NORA P.; GLEMBOTSKY, ANA C.; CONSTANZA BARONI PIETTO, M.; MÉNDEZ-HUERGO, SANTIAGO P.; PIERDOMINICI, MARTA S.; MONTERO, VERÓNICA S.; RABINOVICH, GABRIEL A.; MOLINAS, FELISA C.; HELLER, PAULA G.; LEV, PAOLA R.; MARTA, ROSANA F.

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

Scientific Reports; Año: 2019 vol. 9

GRODZIELSKI, MATÍAS; DI BUDUO, CHRISTIAN A.; GOETTE, NORA P.; LEV, PAOLA R.; SOPRANO, PAOLO M.; HELLER, PAULA G.; BALDUINI, ALESSANDRA; MARTA, ROSANA F.

Autoantibodies in immune thrombocytopenia affect the physiological interaction between megakaryocytes and bone marrow extracellular matrix proteins

BRITISH JOURNAL OF HAEMATOLOGY; Año: 2018

SCHLEGELBERGER, BRIGITTE; HELLER, PAULA G.

RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)

SEMINARS IN HEMATOLOGY; Año: 2017 vol. 54 p. 75 - 80

DE ROCCO, DANIELA; MELAZZINI, FEDERICA; MARCONI, CATERINA; PECCI, ALESSANDRO; BOTTEGA, ROBERTA; GNAN, CHIARA; PALOMBO, FLAVIA; GIORDANO, PAOLA; COCCIOLI, MARIA SUSANNA; GLEMBOTSKY, ANA C.; HELLER, PAULA G.; SERI, MARCO; SAVOIA, ANNA; NORIS, PATRIZIA

Mutations of RUNX1 in families with inherited thrombocytopenia

AMERICAN JOURNAL OF HEMATOLOGY; Año: 2017 vol. 92 p. 86 - 88

BOTTEGA, ROBERTA; NICCHIA, ELENA; ALFANO, CATERINA; GLEMBOTSKY, ANA C.; PASTORE, ANNALISA; BERTAGGIA-CALDERARA, DEBORA; BISIG, BETTINA; DUCHOSAL, MICHEL A.; ARBESÚ, GUILLERMO; ALBERIO, LORENZO; HELLER, PAULA G.; SAVOIA, ANNA

Gray platelet syndrome: Novel mutations of the NBEAL2 gene

AMERICAN JOURNAL OF HEMATOLOGY; Año: 2017 vol. 92 p. 20 - 22

SALIM, JUAN P.; GLEMBOTSKY, ANA C.; LEV, PAOLA R.; MARIN OYARZÚN, CECILIA P.; GOETTE, NORA P.; MOLINAS, FELISA C.; MARTA, ROSANA F.; HELLER, PAULA G.

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

PLATELETS; Año: 2017 vol. 28 p. 602 - 606

ORSINI, SARA; NORIS, PATRIZIA; BURY, LOREDANA; HELLER, PAULA G; SANTORO, CRISTINA; KADIR, REZAN A; BUTTA, NORA C; FALCINELLI, EMANUELA; CID, ANA ROSA; FABRIS, FABRIZIO; FOUASSIER, MARC; MIYAZAKI, KOJI; LOZANO, MARIA LUISA; ZUÑIGA, PAMELA; FLAUJAC, CLAIRE; PODDA, GIAN MARCO; BERMEJO, NURIA; FAVIER, REMI; HENSKENS, YVONNE; DE MAISTRE, EMMANUEL; DE CANDIA, ERICA; MUMFORD, ANDREW D; OZDEMIR, NIHAL G; EKER, IBRAHIM; NURDEN, PAQUITA; BAYART, SOPHIE; LAMBERT, MICHELE P; BUSSEL, JAMES; ZIEGER, BARBARA; TOSETTO, ALBERTO; MELAZZINI, FEDERICA; GLEMBOTSKY, ANA C; PECCI, ALESSANDRO; CATTANEO, MARCO; SCHLEGEL, NICOLE; GRESELE, PAOLO

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

HAEMATOLOGICA; Año: 2017 vol. 102 p. 1192 - 1203

ANTONY-DEBRÉ I ; DUPLOYEZ N; BUCCI M; GEFFROY S; MICOL JB; RENNEVILLE A; BOISSEL N; DHÉDIN N; RÉA D; NELKEN B; BERTHON C; LEBLANC T; MOZZICONACCI MJ; FAVIER R; HELLER PG; ABDEL-WAHAB O; RASLOVA H; LATGER-CANNARD V; PREUDHOMME C

Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia.

LEUKEMIA; Lugar: Londres; Año: 2016 vol. 30 p. 999 - 1002

MELA OSORIO MJ; FERRARI LUCIANA; GOETTE NORA P; GUTIERREZ MI; GLEMBOTSKY AC; MALDONADO C; LEV PAOLA R; ALVAREZ CLARISA; 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: 2016 vol. 96 p. 435 - 442

DI BUDUO CRISTIAN; ALBERELLI MA; GLEMBOTSKY AC; PODDA G; LEV PRI; 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 vol. 6

GOETTE NORA P; GLEMBOTSKY AC; LEV PR; GRODZIELSKI MATÍAS; CONTRUFO G; PIERDOMINICI M; ESPASANDIN YR; RIVEROS D; GARCÍA 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 vol. 11 p. 1 - 14

MARIN OYARZÚN, CECILIA P.; CARESTIA, AGOSTINA; LEV, PAOLA R.; GLEMBOTSKY, ANA C.; CASTRO RÍOS, MIGUEL A.; MOIRAGHI, BEATRIZ; MOLINAS, FELISA C.; MARTA, ROSANA F.; SCHATTNER, MIRTA; HELLER, PAULA G.

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

Scientific Reports; Año: 2016 vol. 6

VERVER, EVA J.J.; TOPSAKAL, VEDAT; KUNST, HENRICUS P.M.; HUYGEN, PATRICK L.M.; HELLER, PAULA G.; PUJOL-MOIX, NURIA; SAVOIA, ANNA; BENAZZO, MARCO; FIERRO, TIZIANA; GROLMAN, WILKO; GRESELE, PAOLO; PECCI, ALESSANDRO

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients with MYH9-Related Disease

EAR AND HEARING; Año: 2016 vol. 37 p. 112 - 120

ESPASANDIN YESICA R; GLEMBOTSKY ANA C; GRODZIELSKI MATÍAS; LEV PAOLA R; GOETTE NORA P; MOLINAS FELISA C; MARTA ROSANA F; HELLER PAULA G

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

LAROCCA LM; HELLER PG; PODDA G; 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 vol. 26 p. 751 - 757

NOETZLI L; LO RW; LEE-SHERICK AB; CALLAGHAN M; NORIS P; SAVOIA A; RAJPURKAR M; JONES K; GOWAN K; BALDUINI CL; PECCI A; GNAN C; DE ROCCO D; DOUBEK M; LI L; LEUNG R; LANDOLT-MARTICORENA C; HUNGER S; HELLER P; GUTIERREZ-HARTMANN A; XIAYUAN L; PLUTHERO FG; ROWLEY JW; WEYRICH AS; KAHR WH; PORTER CC; DI PAOLA J

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

NATURE GENETICS; Lugar: Londres; Año: 2015 vol. 47 p. 535 - 538

PECCI A; KLERSY C ; GRESELE P; LEE K; DE ROCCO D ; BOZZI V; RUSSO G ; HELLER PG; LOFFREDO F ; BALLMAIER M; FABRIS F; BEGGIATO E; KAHR W; PUJOL-MOIX N ; PLATOKOUKI H ; VAN GEET C ; NORIS P; YERRAM P; HERMANS C ; BERNHARD GERBER B; ECONOMOU M; DE GROOT M; ZIEGER B ; DE CANDIA E; FRATICELLI V; KERSSEBOOM R; PICCOLI G; ZIMMERMANN S; FIERRO T; GLEMBOTSKY AC; VIANELLO F; ZANINETTI C; NICCHIA E; GÜTHNER C; BARONCI C; SERI M; KNIGHT P; 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 ANA C; BLUTEAU D; ESPASANDIN YESICA R; GOETTE NORA P; MARTA ROSANA F; MARIN OYARZUN C; KORIN LAURA; LEV PAOLA R; LAGUENS RUBÉN; MOLINAS FELISA C; RASLOVA H; HELLER PAULA G

Mechanisms underlying platelet function defect in a pedigree with FPD/AML: potential role for candidate RUNX1-targets

JOURNAL OF THROMBOSIS AND HAEMOSTASIS; Lugar: Londres; Año: 2014 vol. 12 p. 761 - 772

LEV PAOLA R; GRODZIELSKI MATÍAS; GOETTE NORA P; GLEMBOTSKY ANA C; ESPASANDIN YESICA R; PERDOMINICI M; CONTRUFO GERALDINE; MONTERO V; FERRARI LUCIANA; MOLINAS FELISA C; HELLER PAULA G; MARTA ROSANA F

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; EUROPEAN HEMATOLOGY ASSOCIATION SCIENTIFIC WORKING GROUP ON THROMBOCYTOPENIAS AND PLATELET FUNCTION DISORDERS

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

SAVOIA A ; KUNISHIMA S; DR ROCCO D; ZIEGER B; RAND M; PUJOL-MOIX N; CALISKAN U; TOKGOZ H; PECCI A; NORIS P; SRIVASTAVA A; WARD C; MOREL-KOPP MC; ALESSI MC; BELLUCCI S ; BEURRIER P; DE MAISTRE E; FAVIER R; HÉZARD N; HURTAUD-ROUX MF; LATGER-CANNARD V; LAVENU-BOMBLED C; PROULLE V; MEUNIER S; NÉGRIER C; NURDEN A, NURDEN A, RANDRIANAIVO H, FABRIS F, PLATOKOUKI H, ROSENBERG N, HADJKACEM B, HELLER PG, KARIMI M, BALDUINI CL, PASTORE A, LANZA F., FABRIS F, PLATOKOUKI H, ROSENBERG N, HADJKACEM B, HELLER PG, KARIMI M, BALDUINI CL, PASTORE A, LANZA F.; RANDRIANAIVO H ; FABRIS F; PLATOKOUKI H; ROSENBERG N; HADJKACEM B; HELLER PG; KARIMI M; BALDUINI CL; PASTORE A; LANZA F

Spectrum of the mutations in Bernard-Soulier syndrome

HUMAN MUTATION; Lugar: New York; Año: 2014 vol. 35 p. 1033 - 1045

NORIS P; BIINO G; CIVASCHI E; SAVOIA A; SERI M; MELAZZINI F; LOFFREDDO G; RUSSO G; BOZZI V; NOTARANGELO LG; GRESELE P; HELLER PG; PUJOL-MOIX N; KUNISHIMA S; CATTANEO M; BUSSEL J; DE CANDIA E; CAGIONI C; RAMENGHI U; BAROZZI S; FABRIS F; BALDUINI CL

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

BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY - ONLINE; Año: 2014 vol. 124 p. 4 - 10

DE ROCCO DANIELA; ZIEGER BARBARA; PLATOKOUKI HELEN; HELLER PAULA G; PASTORE ANNALISA; BOTTEGA ROBERTA; NORIS PATRIZIA; BAROZZI SERENA; GLEMBOTSKY ANA C; PERGANTOU HELEN; BALDUINI CARLO L; SAVOIA ANNA; PECCI ALESSANDRO

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

BOTTEGA ROBERTA; PECCI ALESSANDRO; DE CANDIDA ERICA; PUJOL MOIX NURIA; HELLER PAULA G; NORIS PATRIZIA; DE ROCCO DANIELA; PODDA GIAN MARCO; GLEMBOTSKY ANA C; CATTANEO MARCO; BALDUINI CARLO L; SAVOIA ANNA

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

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

NORIS P; FAVIER R; ALESSI MC; GEDDIS A; KUNISHIMA S; HELLER PG; GIORDANO P; NIEDERHOFFER K; BUSSEL J; PODDA G; VIANELLI N; KERSSERBOOM R; PECCI A; GNAN C; MARCONI C; AUVRIGNON A; COHEN W; YU G; IUCHI A; MILLER IMAHIYEROBO A; BOEHLEN F; GHALLOUSSI D; DE ROCCO D; MAGINI P; CIVASCHI E; BIINO G; SERI M; SAVOIA A; BALDUINI C

ANKRD26-related thrombocytopenia and myeloid malignancies.

BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY - ONLINE; Año: 2013 vol. 122 p. 1987 - 1989

BLUTEAU D; GLEMBOTSKY ANA C; RAIMBAULT A; BALAYN N; GILLES L; RAMEAU P; NURDEN P; ALESSI MC; DEBILI N; VAINCHENKER W; HELLER PAULA G; 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 - ONLINE; Lugar: Washington; Año: 2012 vol. 120 p. 2708 - 2718

GLEMBOTSKY ANA C; MARTA ROSANA F; PECCI ALESSANDRO; DE ROCCO DANIELA; GNAN CHIARA; ESPASANDIN YESICA R; GOETTE NORA P; NEGRO FERNANDO D; NORIS PATRICIA; SAVOIA ANNA; BALDUINI CARLO L; MOLINAS FELISA C; HELLER PAULA G

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

LEV PAOLA R; GOETTE NORA P; GLEMBOTSKY ANA C; LAGUENS RUBÉN; CABEZA-MECKERT PATRICIA; SALIM JUAN P; HELLER PAULA G; POZNER ROBERTO G; MARTA ROSANA F; MOLINAS FELISA C

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

PLATELETS; Lugar: Londres; Año: 2011 vol. 22 p. 26 - 36

SAVOIA ANNA; DE ROCCO D; PANZA EMANUELE; BOZZI V; SCANDELLARI R; LOFFREDO G; MUMFORD A; HELLER PAULA G; NORIS PATRICIA; DE GROOT MR; GIANI M; FREDDI P; SCOGNAMIGLIO F; RIONDINO S; PUJOL-MOIX N; FABRIS F; SERI M; BALDUINI CL; PECCI ALESSANDRO

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

THROMBOSIS AND HAEMOSTASIS; Lugar: Stuttgart, Alemania; Año: 2010 vol. 103 p. 826 - 832

GOETTE NORA P; LEV PAOLA R; HELLER PAULA G; KORNBLIHTT LAURA I; KORIN LAURA; MOLINAS FELISA C; MARTA ROSANA F

Monocyte IL-2Ralpha expression is associated with thrombosis and the JAK2V617F mutation in myeloproliferative neoplasms.

CYTOKINE.; Año: 2010 vol. 51 p. 67 - 72

GOETTE NORA P; LEV PAOLA R; HELLER PAULA G; GLEMBOTSKY ANA C; CHAZARRETA CARLOS D; SALIM JUAN P; MOLINAS FELISA C; MARTA ROSANA F

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

EXPERIMENTAL HEMATOLOGY; Año: 2010 vol. 38 p. 868 - 876

GLEMBOTSKY ANA C; KORIN LAURA; LEV PAOLA R; CHAZARRETA CARLOS D; MARTA ROSANA F; MOLINAS FELISA C; HELLER PAULA G

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: Copenhagen, Dinamarca; Año: 2010 vol. 84 p. 398 - 405

DE ROCCO D; HELLER PAULA G; GIROTTO G; PASTORE A; GLEMBOTSKY ANA C; MARTA ROSANA F; BOZZI V; PECCI ALESSANDRO; MOLINAS FELISA C; SAVOIA ANNA

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

PLATELETS; Lugar: Abingdon, Reino Unido; Año: 2009 vol. 20 p. 598 - 602

SALIM JUAN P; GOETTE NORA P; LEV PAOLA R; CHAZARRETA CARLOS D; HELLER PAULA G; ALVAREZ CLARISA L; MOLINAS FELISA C; MARTA ROSANA F

Dysregulation of stromal derived factor 1/ CXCR4 axis in the megakaryocytic lineage in essential thrombocythemia.

BRITISH JOURNAL OF HAEMATOLOGY; Año: 2009 vol. 144 p. 69 - 77

HELLER PAULA G; GLEMBOTSKY ANA C; GOETTE NORA P; MARTA ROSANA F; LEV PAOLA R; MOLINAS FELISA C

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

JOURNAL OF THROMBOSIS AND HAEMOSTASIS; Año: 2008 vol. 6 p. 2215 - 2217

PECCI ALESSANDRO; PANZA EMANUELE; PUJOL-MOIX NÚRIA; KLERSY CATHERINE; DI BARI FILOMENA; BOZZI VALERIA; GRESELE PAOLO; LETHAGEN STEFAN; FABRIS FABRIZIO; DUFOUR CARLO; GRANATA ANTONIO; DOUBEK MICHAEL; PECORARO CARMINE; KOIVISTO PASI A; HELLER PAULA G; IOLASCON ACHILLE; ALVISI PATRIZIA; SCHWABE DIRK; DE CANDIA ERICA; ROCCA BIANCA; RUSSO UMBERTO; RAMENGHI UGO; NORIS PATRIZIA; SERI MARCO; BALDUINI CARLO L; SAVOIA ANNA

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

HUMAN MUTATION; Año: 2008 vol. 29 p. 409 - 417

KORNBLIHTT LAURA I; VASSALLU PATRICIA S; HELLER PAULA G; LAGO NR; ALVAREZ CLARISA L; MOLINAS FELISA C

Primary myelofibrosis in a patient who developed primary biliary cirrhosis, autoimmune hemolytic anemia and fibrillary glomerulonephritis.

ANNALS OF HEMATOLOGY; Año: 2008 vol. 87 p. 1019 - 1020

HELLER PAULA G; PECCI ALESSANDRO; GLEMBOTSKY ANA C; SAVOIA ANNA; NEGRO FERNANDO D; BALDUINI CARLO L; MOLINAS FELISA C

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

PLATELETS; Año: 2006 vol. 17 p. 274 - 275

HELLER PAULA G; LEV PAOLA R; SALIM JUAN P; KORNBLIHTT LAURA I; GOETTE NORA P; CHAZARRETA CARLOS D; GLEMBOTSKY ANA C; VASSALLU PATRICIA S; MARTA ROSANA F; MOLINAS FELISA C

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

EUROPEAN JOURNAL OF HAEMATOLOGY; Año: 2006 vol. 77 p. 210 - 216

HELLER PAULA G; GLEMBOTSKY ANA C; GANDHI MANISH J; CUMMINGS CARRIE L; PIROLA CARLOS J; MARTA ROSANA F; KORNBLIHTT LAURA I; DRACHMAN JONATHAN G; MOLINAS FELISA C

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

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

LEV PAOLA R; SALIM JUAN P; KORNBLIHTT LAURA I; PIROLA CARLOS J; MARTA ROSANA F; HELLER PAULA G; MOLINAS FELISA C

PDGF-A, PDGF-B, TGFbeta and bFGF mRNA levels in patients with essential thrombocythemia treated with anagrelide

AMERICAN JOURNAL OF HEMATOLOGY; Año: 2005 vol. 78 p. 155 - 157

KORNBLIHTT LAURA I; COCORRULLO SILVIA; MIRANDA CARLOS; LYLYK PEDRO; HELLER PAULA G; MOLINAS FELISA C

Moyamoya syndrome in an adolescent with essential thrombocythemia: successful intracraneal carotid stent placement

STROKE; Año: 2005 vol. 36 p. 71 - 73

FINKIELMAN JAVIER D; DE FEO FABIÁN D; HELLER PAULA G; AFESSA BEKELE

The clinical course of patients with septic abortion admitted to an intensive care unit

INTENSIVE CARE MEDICINE; Año: 2004 vol. 30 p. 1097 - 1102

MARTA ROSANA F; GOETTE NORA P; LEV PAOLA R; HELLER PAULA G; KORNBLIHTT LAURA I; VASSALLU PATRICIA S; GLEMBOTSKY ANA C; PIROLA CARLOS J; MOLINAS FELISA C

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

HAEMATOLOGICA; Año: 2004 vol. 89 p. 657 - 663

GARGALLO PATRICIA; HAGEMEIJER ANNE; VASSALLU PATRICIA S; KORNBLIHTT LAURA I; HELLER PAULA G; MOLINAS FELISA C; LARRIPA IRENE

Insertion (4;11)(q27;q24q21) in a patient with essential thrombocythemia with progression to myelofibrosis

CANCER GENETICS AND CYTOGENETICS; Año: 2004 vol. 154 p. 72 - 76

KORNBLIHTT LAURA I; HELLER PAULA G; CORREA GABRIEL; CASTAÑÓN MARÍA M; GENOUD VALERIA; VASSALLU PATRICIA S; SARANO JUDITH; KORDICH LUCÍA; MOLINAS FELISA C

Associated thrombophilic defects in essential thrombocythemia: their relationship with clinical manifestations

THROMBOSIS RESEARCH; Año: 2003 vol. 112 p. 131 - 135

KORNBLIHTT LAURA I; VASSALLU PATRICIA S; HELLER PAULA G; MOLINAS FELISA C

Diez años de experiencia con anagrelide en el tratamiento de la Trombocitemia Esencial

MEDICINA (BUENOS AIRES); Año: 2002 vol. 62 p. 231 - 236

HELLER PAULA; KORNBLIHTT LAURA I; CUELLO MARÍA T; LARRIPA IRENE; NAJFELD VESNA; MOLINAS FELISA C

BCR-ABL transcripts may be detected in essential thrombocythemia but lack clinical significance

BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY - PRINT; Año: 2001 vol. 98 p. 1990 - 1990

GRIMBERG ALEJANDRO R; HELLER PAULA G; CORREA GABRIEL; SARANO J; MOLINAS FELISA; NICASTRO MARIO A; ALVAREZ CLARISA

Sindrome antifosfolipídico catastrófico. Comunicación de dos formas de presentación

MEDICINA (BUENOS AIRES); Año: 1999 vol. 59 p. 743 - 746

HELLER PAULA G; GRIMBERG ALEJANDRO R; LENCIONI MELISA; MOLINA MARÍA M; RONCORONI AQUILES J

Pulmonary Hypertension in Paroxysmal Nocturnal Hemoglobinuria

CHEST; Año: 1992 vol. 102 p. 642 - 643