Cargando…

Sickle Cell Disease: quality of life in patients with hemoglobin SS and SC disorders

OBJECTIVE: Sickle cell disease comprises chronic, genetically determined disorders, presenting significant morbidity and high prevalence in Brazil. The goal of this study was to evaluate the quality of life of sickle cell disease patients (hemoglobin SS and SC) and their sociodemographic and clinica...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pereira, Sônia Aparecida dos Santos, Brener, Stela, Cardoso, Clareci Silva, Proietti, Anna Bárbara de Freitas Carneiro
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Associação Brasileira de Hematologia e Hemoterapia 2013
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3832312/ https://www.ncbi.nlm.nih.gov/pubmed/24255615 http://dx.doi.org/10.5581/1516-8484.20130110

Ejemplares similares

Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC)
por: da Guarda, Caroline Conceição, et al.
Publicado: (2020)

Unrecognized hemoglobin SC sickle cell disease complicated by sepsis and cholestasis
por: McFarland, Thomas, et al.
Publicado: (2022)

HemoTypeSC point-of-care testing shows high sensitivity with alkaline cellulose acetate hemoglobin electrophoresis for screening hemoglobin SS and SC genotypes
por: Adegoke, Samuel Ademola, et al.
Publicado: (2022)

Retinal thickness measurements in sickle cell patients with HbSS and HbSC genotype
por: Lim, Wei S., et al.
Publicado: (2018)

Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles
por: Aleluia, Milena Magalhães, et al.
Publicado: (2017)

Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients
por: Garnier, Yohann, et al.
Publicado: (2017)

Identification of a Small Molecule that Increases Hemoglobin Oxygen Affinity and Reduces SS Erythrocyte Sickling
por: Nakagawa, Akito, et al.
Publicado: (2014)

Glomerular filtration rate is altered in children with sickle cell disease: a comparison between Hb SS and Hb SC
por: de Paula, Rafael Pereira, et al.
Publicado: (2013)

Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)
por: Brewin, John N., et al.
Publicado: (2020)

A Retrospective Analysis of the Significance of Haemoglobin SS and SC in Disease Outcome in Patients With Sickle Cell Disease and Dengue Fever()()
por: Rankine-Mullings, Angela, et al.
Publicado: (2015)

Sociodemographic aspects and quality of life of patients with sickle cell anemia
por: dos Santos, Juliana Pereira, et al.
Publicado: (2013)

Sickle Cells Abolish Melanoma Tumorigenesis in Hemoglobin SS Knockin Mice and Augment the Tumoricidal Effect of Oncolytic Virus In Vivo
por: Sun, Chiang Wang, et al.
Publicado: (2016)

THE STATE OF HEMOGLOBIN IN SICKLED ERYTHROCYTES
por: Stetson, Chandler A.
Publicado: (1966)

Fetal hemoglobin and hemolysis markers in sickle cell anemia()
por: Colella, Marina Pereira, et al.
Publicado: (2015)

Barriers experienced in self-care practice by young people with sickle cell disease
por: Cecilio, Sumaya Giarola, et al.
Publicado: (2018)

Perspectives and challenges to discovering hemoglobin-inducing agents in Sickle Cell Disease
por: Pavan, Aline Renata, et al.
Publicado: (2022)

Sickle Cell Disease and Fetal Hemoglobin
por: Rivera, Alicia
Publicado: (2018)

Hemoglobin SC smear recorded with a smartphone
por: Trikalinos, Nikolaos A., et al.
Publicado: (2016)

Enteric Fever Unmasking Hemoglobin SC Disease
por: Arango-Ferreira, Catalina, et al.
Publicado: (2021)

Symptoms of depression, anxiety and stress in health students and impact on quality of life
por: de Freitas, Pedro Henrique Batista, et al.
Publicado: (2023)

GELS OF NORMAL AND SICKLED HEMOGLOBIN : COMPARATIVE STUDY
por: White, James G., et al.
Publicado: (1970)

Assessment of the quality of life and mental health of healthcare students during the COVID-19 pandemic
por: de Freitas, Pedro Henrique Batista, et al.
Publicado: (2023)

Acute macular infarctions in pediatric patients with hemoglobin SS disease
por: Lee, Patrick SY., et al.
Publicado: (2023)

Bone marrow necrosis and fat embolism syndrome: a dreadful complication of hemoglobin sickle cell disease
por: Targueta, Eduardo Pelegrineti, et al.
Publicado: (2017)

Rapid and inefficient kinetics of sickle hemoglobin fiber growth
por: Castle, Brian T., et al.
Publicado: (2019)

Hemoglobin level and macular thinning in sickle cell disease
por: Hussnain, S Amal, et al.
Publicado: (2019)

Acute Chest Syndrome in Pregnant Women with Hemoglobin SC Disease
por: Nomura, Roseli Mieko Yamamoto, et al.
Publicado: (2009)

Massive Ovarian Edema in a Girl with Hemoglobin SC Disease
por: Johannesen, Eric, et al.
Publicado: (2018)

Laboratory and Genetic Biomarkers Associated with Cerebral Blood Flow Velocity in Hemoglobin SC Disease
por: Santiago, Rayra Pereira, et al.
Publicado: (2017)

P-005: COMPARISON OF SICKLE SCAN AND HEMOTYPE SC AS POINT-OF-CARE NEWBORN SCREENING DIAGNOSTICS FOR SICKLE CELL DISEASE IN LUANDA, ANGOLA
por: B., SANTOS, et al.
Publicado: (2022)

Use of an automated pyrosequencing technique for confirmation of sickle cell disease
por: de Martino, Camila Cruz, et al.
Publicado: (2019)

THE PHYSICAL STATE OF HEMOGLOBIN IN SICKLE-CELL ANEMIA ERYTHROCYTES IN VIVO
por: Döbler, Johanna, et al.
Publicado: (1968)

Sickle Retinopathy in a Person with Hemoglobin S/New York Disease
por: Calder, Donovan, et al.
Publicado: (2012)

The Sickle Effect: The Silent Titan Affecting Glycated Hemoglobin Reliability
por: Gordon, Domonick K, et al.
Publicado: (2020)

Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease
por: El Hoss, Sara, et al.
Publicado: (2020)

Hemoglobin and End-Organ Damage in Individuals with Sickle Cell Disease
por: Ershler, William B., et al.
Publicado: (2023)

Mobile Right Atrial Thrombi in a Patient with the Hemoglobin SC Disease
por: Savage, H. O., et al.
Publicado: (2011)

A Triazole Disulfide Compound Increases the Affinity of Hemoglobin for Oxygen and Reduces the Sickling of Human Sickle Cells
por: Nakagawa, Akito, et al.
Publicado: (2018)

Pattern of hemolysis parameters and association with fetal hemoglobin in sickle cell anemia patients in steady state
por: Moreira, Juliane Almeida, et al.
Publicado: (2015)

Levels of inflammatory markers are differentially expressed in sickle cell anemia and sickle cell trait
por: Gomes, Ingrid Cristiane Pereira, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_8bgs820qvmmnaea4id9kejocso