Evidence map›Paper›PMID 42877362›Full record

ArticleBalkan journal of medical genetics : BJMG2026

Application of Fluorescence in situ Hybridization in Malignant Hemopathies: First Experience from Albania.

D Roko, A Babameto-Laku, A Perolla, E Calliku

Abstract read
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

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.

D RokoFaculty of Medicine, "Mother Teresa" University Hospital Center, Clinical Genetics Laboratory Service, Tirana.
A Babameto-LakuFaculty of Medicine, "Mother Teresa" University Hospital Center, Clinical Genetics Laboratory Service, Tirana.
A PerollaFaculty of Medicine, "Mother Teresa" University Hospital Center, Hematology Service, Tirana.
E CallikuFaculty of Medicine, "Mother Teresa" University Hospital Center, Hematology Service, Tirana.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Genetic alterations in genome organization are essential for the clinical evaluation of hematological disorders. Fluorescence in situ hybridization (FISH) enables the detection and determination of the frequency of genetic abnormalities. Objectives: This study aims to apply selected probes as a diagnostic approach to aid in establishing diagnosis, predicting prognosis, and monitoring disease progression. Results: Fluorescence microscopy analysis of inter-phase cells was undertaken at the Laboratory of Molecular Cytogenetics, within the Clinical Genetics Laboratory Service, in a cohort of 330 adult patients with hematological disorders clinically established by the Hematology Service at QSU "Mother Teresa," Tirana, Albania.Detection of the Conclusions: Through the identification of specific genetic mutations, molecular cytogenetics contributes to early diagnosis, improving the prognosis and choosing the most appropriate treatments, significantly improving the survival and quality of patient's life.

Indexed as

Fluorescence in situ hybridizationpersonalized medicineprobesprognostic factortargeted treatment

Identifiers

PMID42877362
PMCPMC13667941

What OpenQuestion holds

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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.