beta-thalassemia/fatigue

Врската е зачувана во таблата со исечоци

Изберете вид на сортирање

11 резултати

Determining and surveying the role of carnitine and folic acid to decrease fatigue in β-thalassemia minor subjects.

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

Beta-thalassemia minor (BTM) patients usually experience fatigue, bone pain complaint, and muscle weakness. Carnitine is an essential protein for transportation of long-chain fatty acids to the matrix for beta-oxidation. BTM patients have abnormally low plasma carnitine concentrations, which results

Impaired acylcarnitine profile in transfusion-dependent beta-thalassemia major patients in Bangladesh.

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

Patients with beta-thalassemia major (BTM) suffer from fatigue, poor physical fitness, muscle weakness, lethargy, and cardiac complications which are related to an energy crisis. Carnitine and acylcarnitine derivatives play important roles in fatty acid oxidation, and deregulation of carnitine and

Cardiac myxoma showing extramedullary hematopoiesis in a patient with beta thalassemia.

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

A 52-year-old woman presented with recurrent episodes of chest pain, shortness of breath, palpitations, and fatigue for three months. Her past medical history was significant for chronic anemia. Physical examination revealed a pansystolic murmur radiating to the left axilla. Her admission workup

Patient- and Caregiver-Reported Burden of Transfusion-Dependent β-Thalassemia Measured Using a Digital Application

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

Background and objective: Transfusion-dependent β-thalassemia (TDT) is a rare genetic disease characterized by a deficiency of functional β-globin, ultimately leading to lifelong dependence on blood transfusions. There is little patient-

A Rare Case of Hemoglobin E/Beta-Thalassemia and Systemic Lupus Erythematosus

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

Systemic lupus erythematosus (SLE) is a systemic autoimmune disease, with multisystemic involvement. Hemoglobin E/beta-thalassemia (HbE/beta-thalassemia) is the genotype responsible for approximately one-half of all severe beta-thalassemia worldwide. When beta-thalassemia and SLE coexist, SLE seems

Delayed hemolytic transfusion reaction with multiple alloantibody (Anti S, N, K) and a monospecific autoanti-JK(b) in intermediate β-thalassemia patient in Tabriz.

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

It appears that delayed hemolytic transfusion reactions may occur several days after the administration of donor red cells is true even though they have been shown to be compatible in cross match tests by the antiglobulin technique. A specific case was observed in our center, which confirms the

BETA THALASSEMIA MINOR PATIENTS: NOT TIRED, BUT DEPRESSED AND ANXIOUS

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

We aimed to investigate whether the severity of fatigue and the incidences of depression and anxiety of patients with beta thalassemia minor (BTm) are different than healthy individuals using Fatigue Severity Scale (FSS) and Hospital Anxiety and Depression Scale (HADS) BTm patients who were followed

A rare example that coinheritance of a severe form of beta-thalassemia and alpha-thalassemia interact in a "synergistic" manner to balance the phenotype of classic thalassemic syndromes.

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

The coinheritance of beta-thalassemia major with the genotype of Hb H disease is extremely rare, with few reported cases. We investigated the hematological, biochemical, biosynthetic, molecular and pathophysiological parameters to evaluate a rare male patient with this compound syndrome. The patient

Hyperchloremic metabolic acidosis due to deferasirox in a patient with beta thalassemia major.

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

OBJECTIVE To report a case of hyperchloremic metabolic acidosis in a patient with beta thalassemia major secondary to treatment with deferasirox due to iron overload. METHODS A 58-year-old white female with beta thalassemia major was admitted with fever, fatigue, abnormal liver function test

Iron-enriched rice: the case for labeling.

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

ABSTRACT Genetically modified rice that incorporates twofold to threefold increased amounts of iron is being developed. The product could provide improved nutrition to iron-deficient persons but may be a health hazard to large numbers of humans who are prone to iron overload. Clinical disorders such

[Hemoglobin O Arab in interaction with beta 0-thalassemia].

Само регистрираните корисници можат да преведуваат статии

Пријавете се / пријавете се

Clinical, hematologic and hemoglobin composition data on the first case of Hb 0-Arab in association with beta 0-thalassemia in Yugoslavia are reported here. The propositus was a 26-years-old female from Strumica who was admitted to the hospital for several times because of anemia,

Придружете се на нашата
страница на Facebook

Herbal & Natural Medicine

Најкомплетната база на податоци за лековити билки поддржана од науката

Работи на 55 јазици
Лекови од билки поддржани од науката
Препознавање на билки по слика
Интерактивна GPS мапа - означете ги билките на локацијата (наскоро)
Прочитајте научни публикации поврзани со вашето пребарување
Пребарувајте лековити билки според нивните ефекти
Организирајте ги вашите интереси и останете во тек со истражувањето на новостите, клиничките испитувања и патентите

Напишете симптом или болест и прочитајте за билки што можат да помогнат, напишете билка и видете болести и симптоми против кои се користи.
* Сите информации се базираат на објавени научни истражувања