Results 111 to 120 of about 722,667 (218)
Medical Laboratory Journal, 2013 Background and Objective: Of the most common hypochromic microcytic anemia are iron deficiency anemia and minor thalassemia, which are common in Iran and their differential diagnosis is extremely important.
s Royani +6 more
doaj
Lycopenemia in a patient with thalassemia minor
Scripta Scientifica Medica, 2019 An 18-year-old girl presented with yellowish discoloration of her palms that had appeared several days earlier. The rest of her skin, mucous membranes and sclera were with normal color. She denied history of anorexia, jaundice, pruritus, loss of appetite, nausea, vomiting, abdominal pain or change in the color of her urine or stool or any other symptom.
openaire +2 more sources
مجله انفورماتیک سلامت و زیست پزشکی, 2019 Introduction: One of the most common types of anemia is Iron deficiency anemia that its main differential diagnosis is β-thalassemia minor. The rapid and accurate screening of β-thalassemia minor has particular importance for pre-marriage medical ...
Samira Noferesti +2 more
doaj
Childbearing through the Lens of Women with Minor Thalassemia: A Qualitative Study. [PDF]
Galen Med J, 2019 Sarayloo K +4 more
europepmc +1 more source
The effect of educational program based on theory of planned behavior on health promotion and childbearing of minor thalassemia couples. [PDF]
J Educ Health Promot, 2019 Sarayloo K +4 more
europepmc +1 more source
Pregnancy outcomes in women with thalassemia major and minor: an observational cross-sectional study [PDF]
Background: Recent advances in the management of thalassemia have significantly improved life. Expectancy and quality of life in patients with this hemoglobinopathy result in a consequent increase in their reproductive potential and desire to have ...
Begum, Umme A. M. +4 more
core +1 more source
Acute Wilson's disease and thalassemia minor: a case report.
, 1984 The case of a 17-year-old Italian girl with thalassemia minor and fatal acute Wilson's disease together with severe hemolysis is reported. The fortuitous(?) occurrence of both genetically determined conditions in the same patient was the source of ...
Rahier, Jacques +4 more
core
, 2019 Thalassemia is one of the most frequent monogenic disorders, leading to impairment in the maturation and survival of red blood cells. The question examined here is whether, and if so, to what extent, people with betathalassemia might also be impaired in ...
Asadi, Yasaman +5 more
core
Mutation analysis of β-thalassemia in East-Western Indian population: a recent molecular approach
, 2017 Parth S Shah,1 Nidhi D Shah,2 Hari Shankar P Ray,3 Nikunj B Khatri,3 Ketan K Vaghasia,3 Rutvik J Raval,4 Sandip C Shah,3 Mandava V Rao5 1Department of Medicine, Lahey Hospital and Medical Center, Boston, MA, 2Department of Pediatrics, Nassau University ...
Khatri NB +7 more
core
Foxo3 gene expression and oxidative status in beta-thalassemia minor subjects
Background: Oxidative stress may aggravate symptoms of hemolytic anemias such as beta-thalassemia. FoxO3 activation results in resistance to oxidative stress in fibroblasts and neuronal cell cultures. Objective: The purpose of this research was to study
Sandra Stella Lazarte +5 more
core +1 more source