Results 141 to 150 of about 21,024 (196)

Successful Treatment of Hepatitis C Virus by Ledipasvir/Sofosbuvir in a Cirrhotic Patient with Sickle Cell Disease and Thalassemia Minor. [PDF]

Case Rep Gastroenterol, 2018
Al Moussawi H, Polavarapu AD, Asti D, Awada Z, Mulrooney S.   +4 more
europepmc   +1 more source

A Comparison between Serum 25-Hydroxyvitamin D3 Levels and Serum Ferritin in Children and Adolescents with Iron Deficiency Anemia, Thalassemia Minor, Thalassemia Major and Healthy People.

Iran J Public Health
Hemmatipour A, Kikhaei B, Jalkani R, Ahmadnejad M, Soleimanzadeh F, Rokhafrooz D.   +5 more
europepmc   +1 more source

HBG2 -158 (C>T) polymorphism and its contribution to fetal hemoglobin variability in Iraqi Kurds with beta-thalassemia minor. [PDF]

J Lab Physicians, 2018
Albarawi DJ, Balatay AA, Al-Allawi N.
europepmc   +1 more source

Glutaric acidemia type II patient with thalassemia minor and novel electron transfer flavoprotein-A gene mutations: A case report and review of literature. [PDF]

World J Clin Cases, 2018
Saral NY, Aksungar FB, Aktuglu-Zeybek C, Coskun J, Demirelce O, Serteser M.   +5 more
europepmc   +1 more source

[Case of thalassemia minor].

Lijecnicki vjesnik, 2002
openaire   +1 more source

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Depression in subjects with beta-thalassemia minor

Annals of Hematology, 2013
Beta-thalassemia minor is a common genetic blood disorder in Mediterranean countries such as Turkey. Additionally, depression is one of the most widespread mental disorders that affect people worldwide, and its prevalence is increasing with co-occurring medical conditions.
Sakir Özgur Keskek, Ali Turhan
exaly   +3 more sources

Genotoxicity assessment in patients with thalassemia minor

Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 2012
Thalassemia is an inherited blood disorder that affects both genders and results in reduced synthesis of hemoglobin, and thus causing anemia. Previous studies have shown that the severe form of this disease, thalassemia major, is associated with genotoxicity.
Omar Khabour
exaly   +3 more sources

Renal tubular dysfunction in β-thalassemia minor

American Journal of Kidney Diseases, 2003
Persons with beta-thalassemia minor usually are symptomless. However, we previously reported renal tubular dysfunction in a patient with beta-thalassemia minor. The aim of this study is to investigate renal function in patients with beta-thalassemia minor.Forty-one subjects with beta-thalassemia minor and 20 sex- and age-matched healthy subjects were ...
Taner Ozgurtas, Uğur Haci Musabak, Mujdat Yenicesu   +2 more
exaly   +4 more sources

Thalassemia Minor and Major: Current Management

Indian Journal of Pediatrics, 2017
Thalassemia is a common genetic disorder. It has been estimated that in India nearly 5 crore people are thalassemia carriers. They are asymptomatic and are detected on blood tests. These people are at same risk of developing iron deficiency anemia as general population and need iron therapy in the presence of iron deficiency anemia.
exaly   +3 more sources

Osteoarthropathy in Thalassemia Minor

Orthopedics, 1985
ABSTRACT: Osteoarthropathy associated with thalassemia minor is rare. The arthritic changes are usually thought to be secondary to bone infarction or erythropoiesis, with decreased trabeculation of the femoral head followed by microfacture and arthritic changes.
D S, Redman, C L, Nelson
openaire   +2 more sources