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Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area

Overview of attention for article published in Orphanet Journal of Rare Diseases, September 2013
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Title
Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area
Published in
Orphanet Journal of Rare Diseases, September 2013
DOI 10.1186/1750-1172-8-143
Pubmed ID
Authors

Mohamad H Qari, Yasser Wali, Muneer H Albagshi, Mohammad Alshahrani, Azzah Alzahrani, Ibrahim A Alhijji, Abdulkareem Almomen, Abdullah Aljefri, Hussain H Al Saeed, Shaker Abdullah, Ahmad Al Rustumani, Khoutir Mahour, Shaker A Mousa

Abstract

Thalassemia syndrome has diverse clinical presentations and a global spread that has far exceeded the classical Mediterranean basin where the mutations arose. The mutations that give rise to either alpha or beta thalassemia are numerous, resulting in a wide spectrum of clinical severity ranging from carrier state to life-threatening, inherited hemolytic anemia that requires regular blood transfusion. Beta thalassemia major constitutes a remarkable challenge to health care providers. The complications arising due to the anemia, transfusional iron overload, as well as other therapy-related complications add to the complexity of this condition. To produce this consensus opinion manuscript, a PubMed search was performed to gather evidence-based original articles, review articles, as well as published work reflecting the experience of physicians and scientists in the Arabian Gulf region in an effort to standardize the management protocol.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 110 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Indonesia 1 <1%
Unknown 109 99%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 13 12%
Student > Master 11 10%
Researcher 10 9%
Student > Ph. D. Student 10 9%
Other 5 5%
Other 17 15%
Unknown 44 40%
Readers by discipline Count As %
Medicine and Dentistry 35 32%
Biochemistry, Genetics and Molecular Biology 8 7%
Nursing and Health Professions 6 5%
Agricultural and Biological Sciences 6 5%
Immunology and Microbiology 2 2%
Other 8 7%
Unknown 45 41%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 18 September 2013.
All research outputs
#15,279,577
of 22,721,584 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,778
of 2,604 outputs
Outputs of similar age
#123,835
of 201,942 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#27
of 37 outputs
Altmetric has tracked 22,721,584 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,604 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.5. This one is in the 23rd percentile – i.e., 23% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 201,942 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 28th percentile – i.e., 28% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 37 others from the same source and published within six weeks on either side of this one. This one is in the 10th percentile – i.e., 10% of its contemporaries scored the same or lower than it.