Cargando…

Impact of sickle cell disease on work activity

INTRODUCTION: Sickle cell disease is a group of conditions caused by anomalous hemoglobin that predisposes people to some clinical syndromes. Because of these recurrent syndromes, patients have difficulty finding and, often, keeping a job. OBJECTIVES: To evaluate the impact of sickle cell disease on...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pires, Rosana Paula, Oliveira, Mário Cézar, Araújo, Lucio Borges, Oliveira, João Carlos, Alcântara, Tânia Machado
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Associação Nacional de Medicina do Trabalho (ANAMT) 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458333/ https://www.ncbi.nlm.nih.gov/pubmed/36127913 http://dx.doi.org/10.47626/1679-4435-2022-641

Ejemplares similares

Repercussions of sickle cell disease and sickle cell ulcers for men inserted in the world of work
por: do Nascimento, Dayse Carvalho, et al.
Publicado: (2023)

The impact of COVID-19 in children with Sickle Cell Disease: Results of a multicentric registry
por: Oliveira, Claudia de Melo, et al.
Publicado: (2023)

Cardiovascular benefits of a home-based exercise program in patients with sickle cell disease
por: de Araujo Junior, Jonas Alves, et al.
Publicado: (2021)

Evaluation of hydroxyurea genotoxicity in patients with sickle cell disease
por: de Oliveira, Emanuel Almeida Moreira, et al.
Publicado: (2019)

Prevalence of people with sickle cell disease and leg ulcers in Brazil: Socioeconomic and clinical overview
por: Spira, Josimare Aparecida Otoni, et al.
Publicado: (2022)

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

Resting blood lactate in individuals with sickle cell disease
por: Petto, Jefferson, et al.
Publicado: (2011)

Physical activity level and performance in the six-minute walk test of children and adolescents with sickle cell anemia
por: Melo, Hugo Nivaldo, et al.
Publicado: (2017)

Mortality by sickle cell disease in Brazil
por: Arduini, Giovanna Abadia Oliveira, et al.
Publicado: (2017)

Leg ulcers in sickle cell disease patients
por: Granja, Paula Dadalti, et al.
Publicado: (2020)

Clinical and laboratory profile of patients with sickle cell anemia
por: Sant’Ana, Phelipe Gabriel dos Santos, et al.
Publicado: (2017)

Craniofacial geometric morphometrics in the identification of patients with sickle cell anemia and sickle cell trait
por: Ferreira, Warli de Brito, et al.
Publicado: (2020)

Impact of neuropathic pain on quality of life in adults with sickle cell disease: observational study
por: Santos, Lismar Fernando Oliveira dos, et al.
Publicado: (2021)

Objectively measured physical activity levels and sedentary time in children and adolescents with sickle cell anemia
por: Melo, Hugo Nivaldo, et al.
Publicado: (2018)

P-083: IMPACT OF ALPHA THALASSEMIA COEXISTENCE ON TRANSFUSION NEED AMONG PATIENTS WITH SICKLE CELL DISEASE
por: A., MADRUGA DE OLIVEIRA LAGROTTA PITTELLA, et al.
Publicado: (2022)

Association of HIV infection with clinical and laboratory characteristics of sickle cell disease
por: Belisário, André Rolim, et al.
Publicado: (2020)

Quality of life of individuals with sickle cell disease followed at referral centers in Alagoas, Brazil
por: Vilela, Rosana Quintella Brandão, et al.
Publicado: (2012)

Sickle Cell Anaemia and Malaria
por: Luzzatto, Lucio
Publicado: (2012)

Pain measurement as part of primary healthcare of adult patients with sickle cell disease
por: Signorelli, Andreza Aparecida Felix, et al.
Publicado: (2013)

Doppler velocimetry of the orbital arteries in patients with sickle cell anemia: relationship with biomarkers of hemolysis
por: Ferrão, Thiago de Oliveira, et al.
Publicado: (2017)

Low bone mass density is associated with hemolysis in brazilian patients with sickle cell disease
por: Baldanzi, Gabriel, et al.
Publicado: (2011)

The sickle cell trait and end stage renal disease in Salvador, Brazil
por: Alladagbin, Dona J., et al.
Publicado: (2018)

Prevalence of enuresis and its impact in quality of life of patients with sickle cell disease
por: Mrad, Flávia Cristina de Carvalho, et al.
Publicado: (2019)

Ectodermal Dysplasia Associated with Sickle Cell Disease
por: Volpato, Luiz Evaristo Ricci, et al.
Publicado: (2014)

The Availability of Iron Is Involved in the Murine Experimental Toxoplasma gondii Infection Outcome
por: Oliveira, Mário Cézar, et al.
Publicado: (2020)

Survival and mortality among users and non-users of hydroxyurea with sickle cell disease
por: de Araujo, Olinda Maria Rodrigues, et al.
Publicado: (2015)

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

Comments on renal abnormalities of sickle cell disease
por: Abbud-Filho, Mario
Publicado: (2013)

Sterile ‘Abscess’ of the Spleen and the Sickle Cell Trait
por: Luzzatto, Lucio
Publicado: (2018)

Interleukin-6 in pregnancy with sickle cell disease
por: Costa, Manuela Freire Hazin, et al.
Publicado: (2019)

Intrahepatic Cholestasis in Sickle Cell Disease: A Case Report
por: Brunetta, Denise Menezes, et al.
Publicado: (2011)

Abnormal transcranial Döppler ultrasonography in children with sickle cell disease
por: Leite, Ana Claudia Celestino Bezerra, et al.
Publicado: (2012)

Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease
por: Menezes, Joelma Figueiredo, et al.
Publicado: (2023)

Vitamin D in children and adolescents with sickle cell disease: an integrative review
por: de Oliveira, Jacqueline Faria, et al.
Publicado: (2015)

A New Long-Term Composite Drug Delivery System Based on Thermo-Responsive Hydrogel and Nanoclay
por: Tipa, Cezar, et al.
Publicado: (2020)

Levels of angiotensin-converting enzyme 1 and 2 in serum and urine of children with Sickle Cell Disease
por: Hsien, Ho Chi, et al.
Publicado: (2021)

Occupational stress and common mental disorders: how do coping strategies work?
por: Machado, Elis Souza, et al.
Publicado: (2022)

Sickle Cell Disease
por: Álvarez, Ofelia, et al.
Publicado: (2020)

Adenotonsillar Hypertrophy in Pre-School Children with Sickle Cell Disease and Diagnostic Accuracy of the Sleep Disturbance Scale for Children
por: Góis, Carlos Rodolfo Tavares de, et al.
Publicado: (2018)

Impact of prematurity and immigration on neonatal screening for sickle cell disease
por: Cortés-Castell, Ernesto, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_hsfhgj74q1sushcov6ih08a0e3