Results 71 to 80 of about 5,832,501 (223)
Prevalence of Hypoparathyroidism (HPT) in Beta Thalassemia Major
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2014 The aim of this study was to assess the parathyroid functions and bone mineral density (BMD) in patients with beta thalassemia and to correlate them with serum ferritin, calcium, phosphorus and alkaline phosphatase levels.This is a case control study which was done on 55 subjects (40 cases and 15 controls) in the age group of 2-18 years.
Khalida Parveen Basha N. +2 more
openaire +3 more sources
International Journal of Laboratory Hematology, EarlyView.ABSTRACT Background Since the 1970s, more than 40 red blood cell–based formulas have been proposed to differentiate β‐thalassaemia trait (BTT) from iron deficiency (ID) and iron deficiency anaemia (IDA), the main causes of microcytic anaemia. In Germany, where haemoglobinopathies are rare in the autochthonous population but increasingly encountered due
Rafid Al‐Nabhan +2 more
wiley +1 more source
Oral isotretinoin for severe acne in beta-thalassemia major
, 2004 A case of severe acne treated with oral isotretinoin in a patient affected with beta-thalassemia major is ...
VIRGILI, Anna +4 more
core +1 more source
Immunity to tetanus in major beta thalassemia patients
Clinical and Experimental Vaccine Research, 2015 Patients with beta thalassemia major are at increased risk for bacterial infections specially splenectomized patients. The aim of this study was to determine the anti-tetanus antibody concentration among patients with beta thalassemia major.The anti-tetanus antibody concentration was investigated in 224 patients with thalassemia major and 224 healthy ...
Abdolreza Sotoodeh Jahromi +1 more
openaire +2 more sources
Transfusion Medicine, EarlyView.Abstract Objective This study aimed to analyse the distribution and demand patterns of antigen‐negative red blood cells (RBCs) in Shandong Province, China (2022–2024), with a focus on ABO blood groups and clinically significant antigens. The research was designed to provide rigorous data for advancing precision transfusion protocols and to establish a ...
Aiping Zhao +7 more
wiley +1 more source
Beta Thalassemia Major Bone Marrow Transplant [PDF]
Bone Marrow Transplant is the only possible cure till now for the genetic disorder thalassemia. Thalassemia Major can be managed by regular blood transfusions and iron chelation, but the quality of life is still poor and individuals suffering from this ...
Anand, Ayush
core +1 more source
Padjadjaran Journal of Dentistry, 2011 Beta major thalassemia is a genetically inherited blood disorder due to a genetic mutation on the polypeptide chains of hemoglobin which is manifested in the growth and development of the tooth.
Indra Primathena +2 more
doaj +1 more source
Highlights on the Luspatercept Treatment in Thalassemia
, 2023 Luspatercept has been shown to act as a ligand trap, selectively suppressing the deleterious effects of GDF11 that blocks terminal erythroid maturation, restoring normal erythroid differentiation and improving anemia in animal models of &beta ...
Yesim Aydinok, Aydinok, Yesim
core +1 more source
Evaluation of Delayed Puberty of Patients with Beta Thalassemia Major in –Diyala Governorate
Diyala Journal of Medicine, 2018 Background: The absence of secondary sexual characteristics are known complications in patients with beta thalassemia major. Objective: Evaluation the effects of frequent blood transfusions on puberty in patients afflicted with beta thalassemia (β ...
Alaa A Mahmud +2 more
doaj +2 more sources
The Journal of Physiology, EarlyView.Abstract figure legend Downregulation of mitotically associated long non‐coding RNA (MANCR) disturbs transcriptome and proteome in endothelial cells, possibly leading to endothelial and vascular dysfunction in preeclampsia. Abstract Preeclampsia (PE) is a hypertensive disorder during pregnancy, which is characterized by a wide spectrum of endothelial ...
Si‐Yan Zhang, Chi Zhou, Jing Zheng
wiley +1 more source