Results 161 to 170 of about 40,118 (285)

Beta O-39 thalassemia gene: a premature termination codon causes beta- mRNA deficiency without affecting cytoplasmic beta-mRNA stability [PDF]

, 1984
R. Keith Humphries, TJ Ley, NP Anagnou, AW Baur, AW Nienhuis   +4 more
openalex   +1 more source

Economic burden of sickle cell disease in Australia

Internal Medicine Journal, Volume 55, Issue 8, Page 1251-1257, August 2025.
Abstract Background Sickle cell disease (SCD) is an inherited condition that impairs red blood cell function, posing a substantial health burden on patients. As the prevalence of SCD in Australia rises due to migration, discussions surrounding treatment and management strategies are becoming more prominent. Aims Australia lacks a dedicated study on the
Steve Nwokeocha, Helen E. Haysom, Cameron Wellard, Tracy Roberts, Mwayi Kachapila, Melissa Chee, Dennis Petrie, Zoe K. McQuilten, Neil Waters, Anthea Greenway, Kylie Mason, Anna Nelson, Zane Kaplan, P. Joy Ho, Erica M. Wood, Adam Irving, on behalf of the Australian Haemoglobinopathy Registry, Sant‐Rayn Pasricha, Gemma Crighton, Jill Finlayson, Jim Vadolas, Merrole Cole‐Sinclair, Carolyn Greely, Juliana Teo, Yvonne Brennan, Tina Louise Carter, Giselle Kidson‐Gerber, Lye Lin Ho, Mimi Yui, Manika Pal, Claire Dowsing, Pasquale Mario Barbaro, Janis Chamerlain   +32 more
wiley   +1 more source

Hemoglobin F and Beta Thalassemia [PDF]

Science, 1967
Thomas G. Gabuzda, David G. Nathan, Martha Kreimer-Birnbaum, Frank H. Gardner, Robin M. Bannerman   +4 more
openaire   +3 more sources

A family with segregating triplicated alpha globin loci and beta thalassemia [PDF]

, 1983
R Galanello, R Ruggeri, E Paglietti, Maria Addis, MA Melis, Antonio Cao   +5 more
openalex   +1 more source

Know your blood: Addressing barriers to preconceptual screening for sickle cell disease

HemaSphere, Volume 9, Issue 8, August 2025.
Ernel Boadi, Alidor Gaspar, Stephen P. Hibbs   +2 more
wiley   +1 more source

Enhancing Rare Disease Awareness and Education Among Medical Professionals and Students in Türkiye

Journal of Evaluation in Clinical Practice, Volume 31, Issue 5, August 2025.
ABSTRACT Purpose Rare diseases (RDs), which are often chronic, degenerative, and life‐threatening conditions, pose significant challenges due to their complexity and limited awareness among healthcare professionals. This study assessed the knowledge, awareness, and educational needs related to RDs among 5th‐ and 6th‐year medical students at Atatürk ...
Öznur Karagöz, Buşranur Tırtır, Dilek Güneş, Özge Özgen, Mustafa Özçetin, Gülbin Gökçay, Gülden F. Gökçay, Abdolrahman S. Nateri, Fatmahan Atalar   +8 more
wiley   +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  

Erythrocyte membrane skeleton abnormalities in severe beta-thalassemia [PDF]

, 1987
Eilat Shinar, O Shalev, EA Rachmilewitz, SL Schrier   +3 more
openalex   +1 more source

Comparison of Right and Left Side Heart Functions in Patients with Thalassemia Major, Patients with Thalassemia Intermedia, and Control Group

Journal of Tehran University Heart Center, 2015
Background: Heart disease is the main cause of mortality and morbidity in patients with beta thalassemia, rendering its early diagnosis vital. We studied and compared echocardiographic findings in patients with beta thalassemia major, patients with beta ...
Noormohammad Noori, Mehdi Mohamadi, Kambiz Keshavarz, SeyedMostafa Alavi, Maziar Mahjoubifard, Yalda Mirmesdagh   +5 more
doaj  

Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia.

, 1975
Y Kan, Janice P. Holland, A M Dozy, Harold Varmus   +3 more
openalex   +1 more source