Search Results - "Diniz, Michelli Silva"
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High Incidence of Neurological Complications in Patients with Sickle Anemia Disease Undergoing Related Myeloablative Allogeneic Hematopoietic Stem Cell Transplantation: Early Diagnosis and Treatment Can Chance the Prognosis
Published in Blood (06-12-2014)“…Introduction: Hematopoietic stem cell transplantation (HSCT) was offered primarily as a therapeutic option for severe sickle cell disease in the context of…”
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Role of Magnetic Ressonance Imaging – T2 in Hereditary Hemochromatosis
Published in Blood (16-11-2012)“…Abstract 2096 Hereditary hemochromatosis (HH) is an autossomic recessive disorder characterized by increased iron absorption. Magnetic resonance imaging – T2*…”
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3
Whole Exome Sequencing of Philadelphia-Negative (Ph-negative) Myeloproliferative Neoplasms (MPNs) and Myelodysplastic/Myeloproliferative Disorders (MDS/MPD)
Published in Blood (06-12-2014)“…Introduction: The development of next-generation sequencing has made it feasible to interrogate the entire genome or exome (coding genome) in a single…”
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Incidence and Impact of Activating Mutations of the RAS-RAF-MEK-ERK Pathway in Patients with Philadelphia-Negative (Ph-negative) Myeloproliferative Neoplasms (MPNs) and Myelodysplastic/Myeloproliferative Disorders–Unclassified (MDS/MPD-U)
Published in Blood (06-12-2014)“…Introduction: Mutations that activate the RAS-RAF-MEK-ERK pathway have long been known to occur in patients with solid tumors and hematological malignancies…”
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5
Genomic Profile of Patients with Triple Negative (JAK2, CALR and MPL) Essential Thrombocythemia and Primary Myelofibrosis
Published in Blood (06-12-2014)“…Introduction: Essential Thrombocythemia (ET) and Primary Myelofibrosis (PMF) are myeloproliferative neoplasms (MPN) with similar driver mutations. The three…”
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The Presence of ASXL1 Mutations As Well As a Total Number of Myeloid Driver Mutations Higher Than Two Is Strongly Associated with the Diagnosis of Primary Myelofibrosis As Opposed to Essential Thrombocythemia
Published in Blood (06-12-2014)“…Introduction: Primary Myelofibrosis (PMF) and Essential Thrombocythemia (ET) are myeloproliferative neoplasms with similar genetic backgrounds. Both diseases…”
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The Role of Labile Plasmatic Iron (LPI) In the Assessment of Iron Overload In β-Thalassemic Patients and Its Correlation with MRI Findings
Published in Blood (19-11-2010)“…Abstract 2072 The labile plasmatic iron (LPI) represents part of non-transferrin-bound iron (NTBI) capable of entering the tissues and causing oxidative…”
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The Role of Labile Plasmatic Iron (LPI) In the Assessment of Iron Overload In β-Thalassemic Patients and Its Correlation with MRI Findings
Published in Blood (19-11-2010)“…Abstract 2072…”
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Non-Invasive Assessment of Pancreatic Iron Stores by Magnetic Resonance Imaging (MRI) in β-Thalassemic Patients
Published in Blood (20-11-2009)“…Abstract 4052 Poster Board III-987 Frequent transfusions of red blood cells are considered standard therapy for patients with β-thalassemia. However, this can…”
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Cardiac iron overload evaluation in thalassaemic patients using T2 magnetic resonance imaging following chelation therapy: a multicentre cross-sectional study
Published in Hematology, Transfusion and Cell Therapy (01-01-2023)“…Magnetic resonance imaging (MRI) T2* technique is used to assess iron overload in the heart, liver and pancreas of thalassaemic patients. Optimal iron…”
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Iron overload in Brazilian thalassemic patients
Published in Einstein (São Paulo, Brazil) (01-06-2011)“…ABSTRACTObjectives:To evaluate the use of magnetic resonance imaging in patients with β-thalassemia and to compare T2* magnetic resonance imaging results with…”
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Iron overload in Brazilian thalassemic patients
Published in Einstein (São Paulo, Brazil) (01-06-2011)“…ABSTRACT Objectives: To evaluate the use of magnetic resonance imaging in patients with β-thalassemia and to compare T2* magnetic resonance imaging results…”
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