Results 221 to 230 of about 63,523 (253)
Some of the next articles are maybe not open access.

Thalassemia

Hematology, 2004
Abstract New developments in the epidemiology, treatment and prognosis of thalassemia have dramatically altered the approach to the care of affected patients, and these developments are likely to have an even greater impact in the next few years.
Alan R, Cohen   +4 more
openaire   +2 more sources

Thalassemias

Pediatric Clinics of North America, 2013
The thalassemia syndromes are hemoglobin disorders that result from significantly reduced or absent synthesis of either the α- or β-globin chains. The result is a chronic hemolytic anemia with ineffective erythropoiesis and bone marrow overstimulation.
Alissa, Martin, Alexis A, Thompson
openaire   +2 more sources

Thalassemia and infertility

Human Fertility, 2016
Beta-thalassemia (BTM) major is the most common haemoglobin disorder in the world, with high prevalence in people of Mediterranean, Arab or Asian origin. It has been estimated that about 1.5% of the global population (80-90 million people) are carriers of BTM.
Castaldi, Maria Antonietta   +1 more
openaire   +5 more sources

Thalassemia and hypercoagulability

Blood Reviews, 2008
Thalassemia is a congenital hemolytic disease caused by defective globin synthesis resulting in decreased quantity of globin chains. Although the life expectancy of beta-thalassemia patients has markedly improved over the last few years, patients still suffer from many complications of this congenital disease.
A. T. Taher   +3 more
openaire   +4 more sources

Thalassemia

Hematology/Oncology Clinics of North America, 2023
Edward J, Benz, Vijay G, Sankaran
openaire   +2 more sources

Thalassemia in Pregnancy

Clinical Obstetrics and Gynecology, 1995
The responsibility of the obstetrician is to identify during the first trimester women who are carriers for thalassemia. When she has been identified, the father of the baby should be screened and if he is also a carrier, the couple should be offered prenatal diagnosis.
Russell K. Laros, Sarah J. Kilpatrick
openaire   +3 more sources

Pathophysiology of thalassemia

Current Opinion in Hematology, 2002
Despite discoveries concerning the molecular abnormalities that led to the thalassemic syndromes, it still is not known how accumulation of excess unmatched alpha-globin in beta thalassemia and beta-globin in alpha thalassemia leads to red blood cell hemolysis in the peripheral blood, and in the beta thalassemias particularly, premature destruction of ...
openaire   +3 more sources

Thalassemia and Pregnancy

The Journal of Perinatal & Neonatal Nursing, 2003
Thalassemia syndromes, hemoglobinopathies characterized by anemia secondary to genetic defects of hemoglobin, are the most common of the genetic blood disorders. The prevalence and severity of the thalassemia syndromes are population dependent, with the type of thalassemia seen dependent on racial background. The health care provider must recognize the
openaire   +3 more sources

Home - About - Disclaimer - Privacy