Results 171 to 180 of about 1,010,620 (323)

A novel globin structural mutant, Showa-Yakushiji (beta 110 Leu-Pro) causing a beta-thalassemia phenotype [PDF]

, 1987
Y Kobayashi, Y Fukumaki, Norio Komatsu, Yoshihito Ohba, Toshihiko Miyaji, Y Miura   +5 more
openalex   +1 more source

Arthritis in beta‐thalassemia minor [PDF]

Arthritis & Rheumatism, 1983
Pedro Fernández Del Vallado, Celso De León, Luis Gorriz, Gabriel Herrero-Beaumont   +3 more
openaire   +3 more sources

Evaluating pregnancy termination rates for fetal chromosome and single gene disorders

Journal of Genetic Counseling, Volume 34, Issue 4, August 2025.
Abstract We report pregnancy termination rates following a variety of fetal diagnoses and determine which factors may influence this decision. We conducted a retrospective chart review of pregnancies diagnosed with a genetic abnormality at a single institution from January 2012 to April 2023.
Madeline J. Herman, Emily B. Rosenfeld, Nicole Kasatkin, Gary A. Heiman, Shama P. Khan, Elena Ashkinadze   +5 more
wiley   +1 more source

Delineation of the molecular basis of delta- and normal HbA2 beta- thalassemia [PDF]

, 1988
Paolo Moi, E. Paglietti, Adele Sanna, C. Brancati, Antonio Tagarelli, R. Galanello, Antonio Cao, Mario Pirastu   +7 more
openalex   +1 more source

Luspatercept in Transfusion‐Dependent β‐Thalassemia: The Benefit Is Real, and So Are the Risks

American Journal of Hematology, Volume 100, Issue 9, Page 1480-1482, September 2025.
Khaled M. Musallam
wiley   +1 more source

FREQUENCY OF BETA THALASSEMIA TRAIT AMONG THE HEALTHY INDIVIDUALS - A SINGLE CENTRE STUDY

Pakistan Armed Forces Medical Journal, 2018
Objective: To determine the frequency of beta thalassemia trait among the asymptomatic healthy individuals. Study Design: Cross sectional study. Place and Duration of Study: This was carried out at Pakistan Air Force (PAF) Hospital Lahore from ...
Muhammad Arif Sadiq, Ahmad Muqeem, Rizwan Yusuf, Asma Bilal   +3 more
doaj  

بررسی وضعیت بهداشت روانی بیماران مبتلا به تالاسمی ماژور در استان مازندران در سال 1385 [PDF]

, 2007
تالاسمی ماژور بیماری ژنتیکی مزمنی است که با علایم و نشانه های یک کم خونی مزمن و شدید مشخص می گردد. مطالعات اندکی در رابطه با جنبه های مختلف روان پزشکی این بیماری و نیازهای مشاوره ای روان پزشکی و اجتماعی بیماران مذکور در دسترس می باشد.
حسینی, سید حمزه, خانی, حسن, رمضانی, میثم, سیدی طبری, سیده فاطمه, قربانی, آمنه, مجدی, محمدرضا, محسنی, فاطمه, منتظری, علی, نریمانی, بهاره   +8 more
core  

Delta beta thalassemia [PDF]

American Journal of Hematology, 2019
openaire   +3 more sources

A Search for Beta Thalassemia Trait in India

Turkish Journal of Hematology, 2012
To the Editor, The beta-thalassemia trait (BTT)—or beta-thalassemia minor—is a heterozygous condition in which only a single beta-globin gene is affected. The estimated prevalence of BTT in different regions of India is reported to vary between 2.7% and 14.9% (mean: 4.5%) [1,2].
openaire   +4 more sources

A Multicenter Retrospective Study of HbH in China Including 1421 Patients Over a 12‐Year Timespan

eJHaem, Volume 6, Issue 4, August 2025.
ABSTRACT Background Hemoglobin H (HbH) disease is a relatively common genetic disorder worldwide. However, the lack of long‐term follow‐up studies involving large patient cohorts has limited our understanding of its clinical features, disease progression, and outcomes.
Hangning Shang, Shijun Xu, Yaqing Zhang, Junbin Liang, Pingping Li, Lihong Zeng, Yufang Gu, Haiying Li, Weiping Wei, Zhen Lu, Zan Chen, Rongying Gong, Xinhua Zhang, Hui Xu, Li Wang   +14 more
wiley   +1 more source