Browsing by Author "Lyra, Isa Menezes"
Now showing items 22-35 of 35
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Polimorfismos nos genes UGT1A1 e BCL11A: Relação com fatores laboratoriais e com a resposta à hidroxiureia em pacientes pediátricos com anemia falciforme
Rahimy, Rifkath Marie Laurence | Date Issued: 2017INTRODUÇÃO: Os níveis séricos de bilirrubina encontram-se frequentemente aumentados em pacientes com anemia falciforme, já acometidos por hemólise exacerbada, favorecendo a agravação do quadro clinico e a ocorrência de ... -
Priapism in sickle cell disease: associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers
Figueiredo, Camylla Vilas Boas et al. | Date Issued: 2021 -
Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease
Menezes, Joelma Figueiredo et al. | Date Issued: 2023 -
Sequence change in the HS2-LCR and Gg-globin gene promoter region of sickle cell anemia patients
Adorno, Elisângela Vitória et al. | Date Issued: 2008 -
Serum haptoglobin and hemopexin levels are depleted in pediatric sickle cell disease patients
Santiago, Rayra Pereira et al. | Date Issued: 2018 -
The association of infection and clinical severity in sickle cell anaemia patients.
Moura Neto, José Pereira de et al. | Date Issued: 2011 -
The beta-globin gene cluster haplotypes in sickle cell anemia patients from Northeast Brazil: a clinical and molecular view.
Adorno, Elisângela Vitória et al. | Date Issued: 2004 -
The C282Y and H63D mutations in the haemochromatosis gene among sickle cell anemia patients from the Northeast of Brazil
Menezes, Joelma Figueiredo et al. | Date Issued: 2010A Hemocromatose Hereditária (HH) é uma doença autossômica recessiva. As mutações C282Y e H63D no gene HFE têm sido associadas à HH. Objetivo: Avaliar as frequências das mutações C282Y e H63D em pacientes com anemia ... -
The DAU Allele and Anti-D Alloimmunization Present With High Frequency in Brazilian Sickle Cell Disease Patients
Moura Neto, Jose Pereira de et al. | Date Issued: 2017 -
The leftward deletion 4.2 KB alpha-thalassemia in two sickle cell anemia siblings
Takahashi, Daniele et al. | Date Issued: 2010A presença da deleção –α thal 3.7Kb está associada com melhor prognóstico de pacientes que possuem anemia falciforme (AF), contudo não existem estudos na literatura a respeito da associação da –α thal 4.2Kb com a evolução ... -
TNF-alpha and IL-8: serum levels and gene polymorphisms (-308G>A and -251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
Cajado, Cyntia et al. | Date Issued: 2011 -
Transcranial Doppler in hemoglobin SC disease
Vieira, Camilo et al. | Date Issued: 2016 -
ßS-Haplotypes in sickle cell anemia patients from Salvador, Bahia, Northeastern Brazil
Gonçalves, Marilda de Souza et al. | Date Issued: 2003 -
ßS-Haplotypes in sickle cell anemia patients from Salvador, Bahia, Northeastern Brazil
Gonçalves, Marilda de Souza et al. | Date Issued: 2003