Evidence map›Paper›PMID 32577047›Full record

ArticleMedical archives (Sarajevo, Bosnia and Herzegovina)2020

Thalassemia Major and Intermedia Patients in East Java do not Show Fetal Hemoglobin Level Difference in Relation to XMNI Polymorphism.

Retno Dwi Wulandari, Diana Lyrawati, Fatchiyah Fatchiyah, Loeki Enggar Fitri

Open access · greenAbstract read
In one paragraph

Article in Medical archives (Sarajevo, Bosnia and Herzegovina), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Retno Dwi WulandariDoctoral Program in Medical Science, Faculty of Medicine, University of Brawijaya, Indonesia.
Diana LyrawatiDepartment of Pharmacy, Faculty of Medicine, University of Brawijaya, Indonesia.
Fatchiyah FatchiyahDepartment of Biology, Faculty of Mathematics and Natural Sciences, University of Brawijaya, Indonesia.
Loeki Enggar FitriDepartment of Parasitology, Faculty of Medicine, University of Brawijaya, Indonesia.
University of Brawijaya · IDUniversitas Wijaya Kusuma Surabaya · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThalassemia is a genetic disorder, which shows, varies phenotype due to genetic modifier.

aimthis study aimed to investigate the difference in HbF level and the relation of HbF level and

methodsforty-eight beta thalassemia patients (28 males and 20 females), consists of 16 TM and 32 TI; mean age, 25.30 year old. Hemoglobin Fetal and HbA

resultsThe frequency of heterozygote (+/-)

conclusionThis study revealed that thalassemia major and thalassemia intermedia patients in East Java showed similar

Indexed as

Adultbeta-ThalassemiaFemaleFetal Hemoglobingamma-GlobinsHemoglobin AHemoglobin A2HeterozygoteHomozygoteHumansIndonesiaMalePolymerase Chain ReactionPolymorphism, GeneticPolymorphism, Restriction Fragment LengthYoung AdultFetal Hemoglobingamma-GlobinsHemoglobin AHemoglobin A2HbF levelintermediamajorthalassemiaXmnI

Identifiers

PMID32577047
PMCPMC7296421
OpenAlexW3023373205

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.