Cargando…

Is sickle cell disease the same everywhere?

Detalles Bibliográficos
Autor principal:	Hankins, Jane
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/PMC3459638/ https://www.ncbi.nlm.nih.gov/pubmed/23049412 http://dx.doi.org/10.5581/1516-8484.20120042

Ejemplares similares

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

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)

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

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

Here, There, and Everywhere: Kinetochore Function on Holocentric Chromosomes
por: Dernburg, Abby F.
Publicado: (2001)

Rare and everywhere: Perspectives on scale-free networks
por: Holme, Petter
Publicado: (2019)

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

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)

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

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

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

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

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

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)

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

Gene deletions of glutathione S-transferase and iron status in sickle cell patients
por: Zamaro, Paula Juliana Antoniazzo
Publicado: (2012)

Red blood cell alloantibodies and autoantibodies: different presentation, same physiopathology()
por: Dinardo, Carla Luana
Publicado: (2018)

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

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 "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)

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)

Living well with kidney disease by patient and care partner empowerment: kidney health for everyone everywhere
por: Kalantar-Zadeh, Kamyar, et al.
Publicado: (2021)

Comments on 'clinical course of 63 children with hereditary spherocytosis: a retrospective study' - with the particular question: 'Should HS be treated the same way throughout the world?'
por: Bolton-Maggs, Paula
Publicado: (2012)

Everywhere
por: Weber, Larry
Publicado: (2011)

Engineered and natural gene drives: mechanistically the same, yet not same in kind
por: Medina, Raul F., et al.
Publicado: (2023)

Mitigating the effect of the COVID-19 pandemic on sickle cell disease services in African countries
por: Dexter, Daniel, et al.
Publicado: (2020)

Hematopoietic stem cell transplantation for Hodgkin's disease
por: Patah, Poliana, et al.
Publicado: (2011)

Disclosure of cancer diagnosis and quality of life in cancer patients: should it be the same everywhere?
por: Montazeri, Ali, et al.
Publicado: (2009)

The SickleGenAfrica Network
por: Ofori-Acquah, Solomon F
Publicado: (2020)

The Langerhans cell histiocytosis: a disease in search of an identity
por: Rodriguez-Galindo, Carlos
Publicado: (2011)

Fractals everywhere
por: Barnley, Michael Fielding
Publicado: (1993)

Statistics Everywhere
por: Neuberg, Donna S.
Publicado: (2018)

EPR Everywhere
por: Biller, Joshua R., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_3q4bkccfrr23etgqlqp74tki4b