Results 61 to 70 of about 1,157,565 (202)

Effect of Beta Thalassemia Trait in Pregnancy

Community Based Medical Journal
A cross-sectional, observational study was conducted to determine the effects of beta thalassemia trait in pregnancy. A total of 150 pregnant women diagnosed with beta thalassemia trait in Bangladesh Navy Ship (BNS) Patenga Hospital, at Chattogram, Bangladesh, having regular antenatal care and delivery, between January and December of 2022, were ...
Marlina Roy, Md Golam Robbani, Rahnuma Karim, Nasrin Hasan   +3 more
openaire   +1 more source

FREQUENCY OF BETA THALASSEMIA TRAIT IN PREGNANT ANEMIC PATIENTS ATTENDING KHYBER TEACHING HOSPITAL, PESHAWAR-PAKISTAN

Khyber Medical University Journal, 2018
OBJECTIVE: To determine the frequency of beta thalassemia trait in pregnant anemic patients attending Khyber Teaching Hospital, Peshawar, Pakistan. METHODS: This descriptive cross sectional study was conducted in Gynecology and Obstetrics Department of ...
Maimoona Qadir, Sohail Amir
doaj  

Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosis

São Paulo Medical Journal
The red cell distribution width (RDW), and another red cell discriminant function incorporating RDW (MCV² x RDW/Hgb x 100) were determined in a group of 30 patients with iron deficiency anemia, 30 patients with beta thalassemia trait, and 30 normal ...
Carmen Silvia Passos Lima, Aparecida Ribeiro de Carvalho Reis, Helena Zerlotti Wolf Grotto, Sara Teresinha Ollala Saad, Fernando Ferreira Costa   +4 more
doaj   +1 more source

Human biomarker navigator

iMeta, Volume 5, Issue 5, October 2026.
The Human Biomarker Navigator integrates the disease continuum, biomarker dynamics, cross‐organ biomarker networks, biomarker classification, and technology‐driven paradigms. It maps how biomarkers link multi‐system physiology and pathology across the nervous, respiratory, endocrine, circulatory, immune, digestive, urinary, reproductive, and ...
Meng‐Yao Li, Qian Zhang, Zijie Wang, Zeping Gui, Jing Liu, Jingda Li, Maojun Jiang, Zukang Chang, Qingqing Han, Bendong Yang, Tariq Saeed, Jun Li, Jinghan Jia, Chenghu Song, Tong Shao, Tianhuan Peng, Xueying Zhang, Pingping Guo, Jun Luo, Gangao Yang, Yuan Wan, Gokhan Zengin, Quan Yuan, Lingru Li, Xiaohui Fan, Yang Luo, Lvyun Zhu, Yanfei Zheng, Wenjun Mao, Wenlong Sun   +29 more
wiley   +1 more source

Diagnosing Beta Thalassemia trait in a developing country

Acta Haematologica Polonica, 2017
Abstract Background Beta Thalassemia trait (BTT) is diagnosed by detecting hemoglobin A2 (HbA 2 ) >3.8% on either High Performance Liquid Chromatography (HPLC) or cellulose acetate electrophoresis (CAE). HPLC is an accurate and reproducible but costly alternative to more conventional CAE which is labor intensive but easy to interpret and inexpensive.
Shan-e- Rauf, Ghassan Umair Shamshad, Fareeha Mushtaq, Saleem Ahmed Khan, Nadir Ali   +4 more
openaire   +1 more source

Prevalence of Beta-Thalassemia Trait and Abnormal Hemoglobins in the Province of Adiyaman, Turkey

, 2012
Background/Aims: Thalassemia is one of the most common hereditary disorders in Turkey. The aim of this study was to determine the prevalence of the beta-thalassemia trait and abnormal hemoglobins in the province of Adiyaman in Turkey.
Tuncdemir, Aygul, Bayram, Suleyman, Rencuzogullari, Eyup, Onderci, Muhittin, Mutalip, Abdullah, Koc, Tuba, Kucuk, Meral Urhan, Atakur, Selman, Faruk, Muslum, Aslan, Sinan, Sevgiler, Yusuf, Genc, Ahmet, Korkmaz, Deniz Tastemir   +12 more
core   +1 more source

Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene

Haematologica, 2001
BACKGROUND AND OBJECTIVES: The degree of globin chain imbalance and tissue hypoxia are important determinants of clinical severity in thalassemia syndromes. Thus phenotypic expression may be modified by interaction of alpha- and beta-thalassemia defects,
J Traeger-Synodinos, I Papassotiriou, C Vrettou, C Skarmoutsou, A Stamoulakatou, E Kanavakis   +5 more
doaj  

Structural Variation Sequencing of 26 Amniotic Fluid Samples With Partial Gene Duplications and Postnatal Follow‐Up of the Fetuses

Prenatal Diagnosis, Volume 46, Issue 11, Page 1732-1745, October 2026.
ABSTRACT Objectives Partial gene duplications (PGDups) are a significant contributor to genetic disease. The precise genomic location and structure of PGDups are often unresolved using conventional methods, so prenatal diagnosis for PGDups is challenging, especially without ultrasound abnormalities.
Shengfang Qin, Xueyan Wang, Mengjia Yan, Yuxia He, Zhuo Zhang, Yan Yin, Jin Wang, Beibei Guo, Jing Wang, Na Xi, Zhaokai Li   +10 more
wiley   +1 more source

Distribution of hemoglobinopathies in patients presenting for electrophoresis and comparison of result with High performance liquid chromatography

Journal of Pathology of Nepal, 2015
Background: Nearly 226 million carriers of thalassemias and abnormal hemoglobin are present worldwide according to the World Health Organization (WHO). The laboratory plays an important role in the investigation of the thalassemias and hemoglobinopathies.
R Jha
doaj   +1 more source

A global survey of blood transfusion practices for patients with sickle cell disease

Transfusion, Volume 66, Issue 10, Page 1926-1938, October 2026.
Abstract Background Sickle cell disease (SCD) affects over 7 million people globally, with blood transfusion remaining a cornerstone of management. However, contemporary transfusion practices across diverse settings remain poorly characterized. We evaluated global transfusion practices for patients with SCD to identify gaps and inform resource ...
Jeremy W. Jacobs, Arwa Z. Al‐Riyami, Jeannie Callum, Meghan Delaney, David Daniel, Jenny White, Christopher Bocquet, Mohammed Farouk, Claude Tayou, Chinelo P. Onyenekwu, Kristina Prus, Divjot Singh Lamba, Julie Makani, Quentin Eichbaum, Luiz Amorim, Silvano Wendel, France Pirenne, Vernon Louw, Evan M. Bloch   +18 more
wiley   +1 more source