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Alessandro Pecci

Showing results (101-110 of 121) with videos related to

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Stem Cell Research & Therapy|July 25, 2015
Ex vivo immunosuppressive effects of mesenchymal stem cells on Crohn's disease mucosal T cells are largely dependent on indoleamine 2,3-dioxygenase activity and cell-cell contactRachele Ciccocioppo, Giuseppina C Cangemi, Peter Kruzliak, et al.
Journal of Thrombosis and Haemostasis : JTH|April 21, 2021
The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet PhysiologyPaolo Gresele, Emanuela Falcinelli, Loredana Bury, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 31, 2004
Low-dose thalidomide ameliorates cytopenias and splenomegaly in myelofibrosis with myeloid metaplasia: a phase II trialMonia Marchetti, Giovanni Barosi, Francesca Balestri, et al.
Blood|July 25, 2009
Endothelial colony-forming cells from patients with chronic myeloproliferative disorders lack the disease-specific molecular clonality markerGiovanna Piaggio, Vittorio Rosti, Mirko Corselli, et al.
Thrombosis and Haemostasis|February 23, 2010
Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorderAnna Savoia, Daniela De Rocco, Emanuele Panza, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2026
Interlaboratory exercise on the use of immunofluorescence microscopy on the blood smear for recognizing inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelets in Health and DiseaseCarlo Zaninetti, Loredana Bury, Valeria Bozzi, et al.
Haematologica|September 22, 2011
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)Patrizia Noris, Silverio Perrotta, Roberta Bottega, et al.
Haematologica|July 2, 2016
Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemiaFederica Melazzini, Flavia Palombo, Alessandra Balduini, et al.
Blood|April 7, 2011
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 familiesPatrizia Noris, Silverio Perrotta, Marco Seri, et al.
American Journal of Human Genetics|January 8, 2011
Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2Tommaso Pippucci, Anna Savoia, Silverio Perrotta, et al.
Pageof 13

Showing results (101-110 of 121) with videos related to

Sort By:
Pageof 13
Stem Cell Research & Therapy|July 25, 2015
Ex vivo immunosuppressive effects of mesenchymal stem cells on Crohn's disease mucosal T cells are largely dependent on indoleamine 2,3-dioxygenase activity and cell-cell contactRachele Ciccocioppo, Giuseppina C Cangemi, Peter Kruzliak, et al.
Journal of Thrombosis and Haemostasis : JTH|April 21, 2021
The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet PhysiologyPaolo Gresele, Emanuela Falcinelli, Loredana Bury, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 31, 2004
Low-dose thalidomide ameliorates cytopenias and splenomegaly in myelofibrosis with myeloid metaplasia: a phase II trialMonia Marchetti, Giovanni Barosi, Francesca Balestri, et al.
Blood|July 25, 2009
Endothelial colony-forming cells from patients with chronic myeloproliferative disorders lack the disease-specific molecular clonality markerGiovanna Piaggio, Vittorio Rosti, Mirko Corselli, et al.
Thrombosis and Haemostasis|February 23, 2010
Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorderAnna Savoia, Daniela De Rocco, Emanuele Panza, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2026
Interlaboratory exercise on the use of immunofluorescence microscopy on the blood smear for recognizing inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelets in Health and DiseaseCarlo Zaninetti, Loredana Bury, Valeria Bozzi, et al.
Haematologica|September 22, 2011
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)Patrizia Noris, Silverio Perrotta, Roberta Bottega, et al.
Haematologica|July 2, 2016
Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemiaFederica Melazzini, Flavia Palombo, Alessandra Balduini, et al.
Blood|April 7, 2011
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 familiesPatrizia Noris, Silverio Perrotta, Marco Seri, et al.
American Journal of Human Genetics|January 8, 2011
Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2Tommaso Pippucci, Anna Savoia, Silverio Perrotta, et al.
Pageof 13