Search Results - "Cançado, R. D."

HFE gene mutations and iron status of Brazilian blood donors by Santos, P C J L, Cançado, R D, Terada, C T, Rostelato, S, Gonzales, I, Hirata, R D C, Hirata, M H, Chiattone, C S, Guerra-Shinohara, E M

“…Mutations of the HFE and TFR2 genes have been associated with iron overload. HFE and TFR2 mutations were assessed in blood donors, and the relationship with…”
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P1491: REAL‐WORLD INCIDENCE OF VASO‐OCCLUSIVE CRISES IN PATIENTS WITH SICKLE CELL DISEASE (SCD) AND A HIGH BASELINE DISEASE BURDEN TREATED WITH CRIZANLIZUMAB: RESULTS FROM A MANAGED ACCESS PROGRAM (MAP) by Silva‐Pinto, A. C., Colombatti, R., Pasanisi, A., Arcioni, F., DeBonnett, L., Soliman, W., Sarkar, R., Cançado, R. D.

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RECURRENT ISOLATED CENTRAL NERVOUS SYSTEM BLAST CRISIS IN A PATIENT WITH CHRONIC MYELOID LEUKEMIA IN COMPLETE MOLECULAR REMISSION AND PREVIOUS TRAUMATIC CEREBROSPINAL FLUID FISTULA: A CASE REPORT by FGL Nunes, F Malagutti, MEP Antoniolli, GG Rodrigues, LOVD Reis, RCS Alves, JS Almeida, TC Bortolheiro, RD Cançado, AC Kneese

“…Backgroud: Chronic myelogenous leukemia (CML) is a clonal myeloproliferative disorder characterized by presence of the Philadelphia (Ph) chromosome. CML has…”
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Iron deficiency and frequency of HFE C282Y gene mutation in Brazilian blood donors by Terada, C. T., Santos, P. C. J. L., Cançado, R. D., Rostelato, S., Lopreato, F. R., Chiattone, C. S., Guerra-Shinohara, E. M.

“…Limited data are available about iron deficiency (ID) in Brazilian blood donors. This study evaluated the frequencies of ID and iron‐deficiency anaemia (IDA)…”
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REAL-WORLD DATA ON THE TREATMENT OF SICKLE CELL DISEASE WITH VOXELOTOR: RESULTS FROM A BRAZIL'S EARLY ACCESS PROGRAM by RD Cancado, ACS Pinto, AS Araujo, CLC Lobo, MS Figureido

“…Introduction: Voxelotor, is a first-in-class modifying therapy approved to treat patients with sickle cell disease (SCD), a once-daily, oral treatment that…”
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Iron deficiency in blood donors by Cançado, R D, Chiattone, C S, Alonso, F F, Langhi Júnior, D M, Alves, R de C

“…Blood donation results in a substantial loss of iron (200 to 250 mg) at each bleeding procedure (425 to 475 ml) and subsequent mobilization of iron from body…”
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Spinal cord compression in beta-thalassemia: follow-up after radiotherapy by da Fonseca, S F, Figueiredo, M S, Cançado, R D, Nakandakare, F, Segreto, R, Kerbauy, J

“…Spinal cord compression due to extramedullary hematopoiesis is a well-described but rare syndrome encountered in several clinical hematologic disorders,…”
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SÍNDROME DE HIPERHEMOLISE EM PACIENTE SEM HEMOGLOBINOPATIAS: UM RELATO DE CASO by MEP Antoniolli, LOVD Reis, F Malagutti, FGL Nunes, GG Rodrigues, D Fujimoto, RD Cançado, JS Almeida, ACKVD Nascimento

“…Introdução/Objetivos: A síndrome de hiperhemólise é uma complicação tardia rara que ocorre mais comumente em paciente com hemoglobinopatias que necessitam de…”
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Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload by de Lima Santos, Paulo Caleb Júnior, Pereira, Alexandre C, Cançado, Rodolfo D, Schettert, Isolmar T, Hirata, Rosario D C, Hirata, Mario H, Figueiredo, Maria Stella, Chiattone, Carlos S, Krieger, Jose E, Guerra-Shinohara, Elvira M

“…most hereditary hemochromatosis (HH) patients are homozygous for the p.C282Y mutation in the HFE gene. Some studies reported that HH phenotypic expression…”
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Guidelines on neonatal screening and painful vaso-occlusive crisis in sickle cell disease: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular: Project guidelines: Associação Médica Brasileira - 2016 by Braga, Josefina Aparecida Pellegrini, Veríssimo, Mônica Pinheiro de Almeida, Saad, Sara Teresinha Olalla, Cançado, Rodolfo Delfini, Loggetto, Sandra Regina

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