Results 91 to 100 of about 1,157,565 (202)

Sickle Cell Disease and Kidney Injury: Circulating Uromodulin Allows Early Tissue Specific Diagnosis and Monitoring of Treatment

American Journal of Hematology, Volume 101, Issue 9, Page 2430-2434, September 2026.
Ferras Alashkar, Robert Hable, Denise Zwanziger, Friederike Poppenborg, Raina Yamamoto, Hans Christian Reinhardt, Alexander Röth, Victor Herbst, Yara Bestmann, Marco Kai, Jürgen E. Scherberich   +10 more
wiley   +1 more source

Chronic hyperplastic anemia as an independent risk factor for atherosclerotic lesions: a lesson from thalassemia intermedia [PDF]

, 2010
Introduction. Cardiovascular involvement represents a well-known complication and the primary cause of mortality, both in transfusion-dependent beta thalassemia major (β-TM) and in transfusion-independent beta thalassemia intermedia (β-TI ...
Pier Luigi Cocco, Alessandra Spiga, Fabrizio Angius, Stefania Vacquer, Maria Eliana Lai, Antonella Mandas, Maria Paola Carta, Sandra Dessi   +7 more
core  

Prevalence of Beta Thalassemia Trait among Antenatal Women Attending a Tertiary Care Centre [PDF]

, 2020
BACKGROUND: Beta thalassemia is an autosomal recessive disorder characterized by a reduced synthesis of globin chains (Beta chains) and as a compensation, gamma or delta globin chain synthesis is increased.
Menaka Devi, M
core  

Prevalence of various types of anemia and thalassemia in pregnant women: experience from Northern India [PDF]

New Indian Journal of OBGYN
Objectives: Anemia amounts to a significant health problem in developing countries especially among pregnant women. The present study was carried out to determine prevalence of various types of anaemia and thalassemia in antenatal women.
Rajesh Kumar Mishra, Ajay Nathan, S D Poddar, Swati Sagarika Panda   +3 more
doaj   +1 more source

Heterozygous Beta Thalassemia in Parents of Children with Beta Thalassemia Major

Gomal Journal of Medical Sciences, 2004
Background: Beta thalassemia is the most common single gene disorder causing a major genetic health problem in the world. Beta thalassemia is common in Pakistan.
Imran-ud-Din Khattak, Sania Tanweer Khattak, Jehanzeb Khan   +2 more
doaj  

Tek tüp osmotik fragilite testi ile beta-thalassemia trait taraması

, 1983
Bu çalışma 1982-1983 öğretim yılında Antalya merkezinde bulunan lise ve dengi okullardaki sağlıklı öğrenciler arasında basit örnekleme yöntemiyle seçilen 1097 öğrencide yapılmıştır.
Canatan, Duran
core  

Acute hemolysis in association with hepatitis B infection in a child with beta-thalassemia trait

, 1994
Autoimmune hemolytic anemia may occur in the course of some viral diseases such as Coxsackie virus, cytomegalovirus, Epstein Barr virus, Influenza A, herpes simplex virus, and rarely hepatitis B virus infection.
Aysel Yüce, Aytemiz Gürgey, Namık Özbek, Nurten Koçak   +3 more
core   +1 more source

Familial Association of Gilberts and Beta Thalassemia Trait

Chattagram Maa-O-Shishu Hospital Medical College Journal, 2014
A 21 yrs old male from Jatrabari, Dhaka became unfit to travel to Gulf, as his serum bilirubin was found 5.7 mg/dl. He was diagnosed to have Thalassemia trait along with Gilbert’s syndrome. His elder brother has also got similar diseases from age 14. Here both associations of these diseases with positive family history are highlighted.DOI: http://dx ...
openaire   +2 more sources

Factors associated with continuing emergence of β-thalassemia major despite prenatal testing: a cross-sectional survey

, 2017
Haleama Al Sabbah,1 Sarah Khan,1 Abdallah Hamadna,2 Lamia Abu Ghazaleh,2 Anwar Dudin,2 Bashar Adnan Karmi3 1College of Natural and Health Sciences, Zayed University, Dubai, UAE; 2Faculty of Medicine, An-Najah National University, Nablus, Palestine ...
Al Sabbah H, Hamadna A, Dudin A, Karmi BA, Abu Ghazaleh L, Khan S   +5 more
core  

Hospital-acquired pneumonia due to Burkholderia cepacia in a thalassemia pregnancy with postoperative eclampsia: A case report

Respiratory Medicine Case Reports
There are limited case reports on individuals infected with Burkholderia cepacia who do not have typical risk factors, particularly pregnant women with beta-thalassemia.
Khoa Nguyen-Dang, Ngoc Duong-Minh, Hanh-Duyen Bui-Thi   +2 more
doaj   +1 more source