Cargando…

Gene deletions of glutathione S-transferase and iron status in sickle cell patients

Detalles Bibliográficos
Autor principal:	Zamaro, Paula Juliana Antoniazzo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Associação Brasileira de Hematologia e Hemoterapia 2012
Materias:	Scientific Comments
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459386/ https://www.ncbi.nlm.nih.gov/pubmed/23049395 http://dx.doi.org/10.5581/1516-8484.20120025

Ejemplares similares

Prevalence of glutathione S-transferase gene deletions and their effect on sickle cell patients
por: Sanjay, Pandey, et al.
Publicado: (2012)

Oxidative status in sickle cell anemia
por: Magalhães, Silvia Maria Meira
Publicado: (2011)

Nitric oxide status in sickle cell anemia
por: Gonçalves, Romélia Pinheiro
Publicado: (2012)

Comments on: "Impact of iron overload on interleukin-10 levels, biochemical parameters and oxidative stress in patients with sickle cell anemia"
por: Driss, Adel
Publicado: (2013)

The Neonatal Screening Program in Brazil, Focus on Sickle Cell Disease (SCD)
por: Silva-Pinto, Ana C., et al.
Publicado: (2019)

Sexuality and sickle cell disease
por: Figueiredo, Maria Stella
Publicado: (2013)

An eye on sickle cell retinopathy()
por: de Melo, Mônica Barbosa
Publicado: (2014)

Is sickle cell disease the same everywhere?
por: Hankins, Jane
Publicado: (2012)

Oxidative stress in sickle cell disease
por: Queiroz, Raphael Ferreira, et al.
Publicado: (2013)

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

Sickle cell disease: looking back but towards the future
por: Cançado, Rodolfo Delfini
Publicado: (2012)

Comment on sickle cell disease and left ventricular hypertrophy()
por: Verissimo, Monica Pinheiro de Almeida
Publicado: (2015)

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

Prostate cancer and glutathione S-transferase deletions
por: Malik, Saima Shakil, et al.
Publicado: (2015)

Comment on "The influence of hydroxyurea on oxidative stress in sickle cell anemia"
por: van Beers, Eduard Johannes, et al.
Publicado: (2012)

Sickle cell anemia: clinical diversity and beta S-globin haplotypes
por: Loggetto, Sandra Regina
Publicado: (2013)

Dynamics of sickle cell disease as one of the determinants of quality of life
por: Ivo, Maria Lúcia, et al.
Publicado: (2013)

Haptoglobin: an emerging candidate for phenotypic modulation of sickle cell anemia?()
por: Santos, Magnun Nueldo Nunes dos
Publicado: (2015)

Comments on: molecular matching of red blood cells is superior to serological matching in sickle cell disease patients
por: Nance, Sandra Taddie, et al.
Publicado: (2013)

Comprehensive healthcare for individuals with sickle cell disease - a constant challenge
por: Cançado, Rodolfo Delfini
Publicado: (2011)

Pregnancy in sickle cell disease – do we know what to expect?()
por: Fertrin, Kleber Yotsumoto
Publicado: (2014)

The invisibility of sickle cell disease in Brazil: lessons from a study in Maranhão()
por: Viana, Marcos Borato
Publicado: (2015)

Sickle cell disease: from the beginning until it was recognized as a public health disease
por: Naoum, Paulo Cesar
Publicado: (2011)

Comment on: “Oral health-related quality of life in children and teens with sickle cell disease”()
por: Correa, Maria Elvira Pizzigatti
Publicado: (2016)

Comment on “Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia”()
por: Souza Goncalves, Marilda
Publicado: (2014)

Comment on "The burden and quality of life of caregivers of sickle cell anemia patients taking hydroxyurea versus those not taking hydroxyurea"
por: Souza, José Carlos, et al.
Publicado: (2012)

Comment on “Influence of βS-globin haplotypes and hydroxyurea on tumor necrosis factor-alpha levels in sickle cell anemia”
por: de Souza Torres, Lidiane
Publicado: (2014)

Comment on: Homocysteine and vitamin B(12) status and iron deficiency anemia in female university students from Gaza, Palestine
por: Al Laham, Nahed Ali
Publicado: (2014)

Quality of life in sickle cell disease: assessments by the 36-item Short Form Health Survey Questionnaire and Beck Depression Inventory
por: Ivo, Maria Lucia, et al.
Publicado: (2012)

Comparing electrophoresis at alkaline pH and high performance liquid chromatography to diagnose Hb S-like hemoglobin
por: de Oliveira, Renan Gracia, et al.
Publicado: (2012)

What influences Hb fetal production in adulthood?
por: Carrocini, Gisele Cristine de Souza, et al.
Publicado: (2011)

Comment on: Evaluation of erythrocyte and reticulocyte parameters as indicative of iron deficiency in patients with anemia of chronic disease()
por: Piva, Elisa
Publicado: (2015)

On the relevance of outpatient intravenous iron therapy for anemia management
por: Muñoz, Manuel
Publicado: (2011)

Challenges in the diagnosis of iron deficiency anemia in aged people()
por: de Moraes, Niele Silva, et al.
Publicado: (2017)

Enrichment of iron and folic acid: the real need and the dangers of this initiative
por: Fisberg, Mauro, et al.
Publicado: (2011)

Comment on “Nutritional status of patients submitted to transplantation of allogeneic hematopoietic stem cells: a retrospective study”()
por: Schmidt, Erin M., et al.
Publicado: (2014)

Adjusting thresholds of serum ferritin for iron deficiency: a moving target()
por: Naoum, Flávio Augusto
Publicado: (2017)

APOL1, Sickle Cell Trait, and Glutathione S-Transferase 1—More Complicated Than It Seems
por: Kruzel-Davila, Etty, et al.
Publicado: (2022)

The synergy of tobacco and alcohol and glutathione S-transferase θ 1 gene deletion and oral squamous cell carcinoma
por: D’ Mello, Sarah, et al.
Publicado: (2016)

Glutathione and glutathione S-transferases in Barrett's epithelium.
por: Peters, W. H., et al.
Publicado: (1993)

Cannot write session to /tmp/vufind_sessions/sess_hrjcbt3akr0n928qo1hp4voh4h