Results 231 to 240 of about 3,873 (265)
Some of the next articles are maybe not open access.
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.
S J, Kilpatrick, R K, Laros
openaire +2 more sources
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.
S J, Kilpatrick, R K, Laros
openaire +2 more sources
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 +4 more sources
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 +4 more sources
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 +2 more sources
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 +2 more sources
JAMA: The Journal of the American Medical Association, 1979
As every schoolchild knows, tea played an important role in the political strategy of the American Revolution. The tea boycott and the Boston Tea Party are matters of recorded history. Less well known is the medical accompaniment to the political performance.
openaire +2 more sources
As every schoolchild knows, tea played an important role in the political strategy of the American Revolution. The tea boycott and the Boston Tea Party are matters of recorded history. Less well known is the medical accompaniment to the political performance.
openaire +2 more sources
PATHOPHYSIOLOGY OF THALASSEMIA
Annals of the New York Academy of Sciences, 1980The clinical manifestations in homozygous thalassemia may be attributed to the defect in hemoglobin synthesis (Figure 16). It is best typified by beta thalassemia, where excess alpha chains accumulate to form intracytoplasmic erythrocytic inclusions. This leads to anemia, bone marrow hyperplasia, osteoporosis, hemosiderosis, and organ failure.
openaire +2 more sources