Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.
about
The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia.Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients.Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.Genetic modifiers of sickle cell diseasePatients with sickle cell disease have increased sensitivity to cold and heat.Sickle cell disease in mice is associated with sensitization of sensory nerve fibers.Characterization of functional brain activity and connectivity using EEG and fMRI in patients with sickle cell disease.Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia.Thinking beyond sickling to better understand pain in sickle cell disease.Clinical and Laboratory Predictors of Frequency of Painful Crises among Sickle Cell Anaemia Patients in Nigeria.The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease PatientsLactate Dehydrogenase: A Marker of the Severity of Vaso-Occlusive Crisis in Children with Sickle Cell Disease Presenting at the Emergency Department.Intravascular hemolysis and the pathophysiology of sickle cell disease.Exploring Transition to Self-Management Within the Culture of Sickle Cell Disease.Tartrate-Resistant Acid Phosphatase 5b in Young Patients With Sickle Cell Disease and Trait Siblings: Relation to Vasculopathy and Bone Mineral Density.Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemiaHypoxia-enhanced adhesion of red blood cells in microscale flow.Endothelial nitric oxide synthase gene intron 4 VNTR polymorphism in sickle cell disease: relation to vasculopathy and disease severity.Increased theta band EEG power in sickle cell disease patients.Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon.Clinical Predictive Value of Cystatin C in Pediatric Sickle Cell Disease: A Marker of Disease Severity and Subclinical Cardiovascular Dysfunction.
P2860
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P2860
Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Markers of severe vaso-occlusi ...... cents with sickle cell anemia.
@ast
Markers of severe vaso-occlusi ...... cents with sickle cell anemia.
@en
type
label
Markers of severe vaso-occlusi ...... cents with sickle cell anemia.
@ast
Markers of severe vaso-occlusi ...... cents with sickle cell anemia.
@en
prefLabel
Markers of severe vaso-occlusi ...... cents with sickle cell anemia.
@ast
Markers of severe vaso-occlusi ...... cents with sickle cell anemia.
@en
P2093
P2860
P50
P1476
Markers of severe vaso-occlusi ...... cents with sickle cell anemia.
@en
P2093
Andrew Campbell
Caterina P Minniti
Craig Sable
Deepika S Darbari
Gregory Ensing
Lori Luchtman-Jones
Manuel Arteta
Mehdi Nouraie
Onyinye Onyekwere
P2860
P304
P356
10.1016/J.JPEDS.2011.07.018
P407
P577
2011-09-03T00:00:00Z