Evidence map›Paper›PMID 41878223›Full record

ArticleNeurology. Genetics2026

Utility of 18F-FDG PET/CT in the Surveillance of Patients With Neurofibromatosis Type 1.

Maria Gabriela Tanase, Lina Djilani, Remy Lamontagne, Rahma Derbel, Mathilde Baril, Vincent Roy, Mathieu Blais, François-Alexandre Buteau, Hélène T Khuong, Francois Gros-Louis and 2 more

Abstract read
In one paragraph

Article in Neurology. Genetics, 2026. 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
–field-weighted citation impact
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.

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

12 authors.

Maria Gabriela TanaseDepartement of Medicine, Université Laval, Québec, Canada.ORCID https://orcid.org/0000-0002-1226-3938
Lina DjilaniDepartement of Medicine, Université Laval, Québec, Canada.ORCID https://orcid.org/0009-0006-1835-7130
Remy LamontagneDepartement of Medicine, Université Laval, Québec, Canada.ORCID https://orcid.org/0009-0002-5006-7054
Rahma DerbelDepartement of Radiology and Nuclear Medicine, CHU de Québec-Université Laval, Canada; and.ORCID https://orcid.org/0009-0006-1003-2892
Mathilde BarilDepartement of Medicine, Université Laval, Québec, Canada.ORCID https://orcid.org/0009-0004-7056-7704
Vincent RoyRegenerative Medicine Division, CHU de Québec-Université Laval, Canada.ORCID https://orcid.org/0000-0003-2583-6376
Mathieu BlaisNeuroscience Division, CHU de Québec-Université Laval, Canada.ORCID https://orcid.org/0009-0001-9102-378X
François-Alexandre ButeauDepartement of Radiology and Nuclear Medicine, CHU de Québec-Université Laval, Canada; and.ORCID https://orcid.org/0000-0002-9667-1460
Hélène T KhuongDepartement of Medicine, Université Laval, Québec, Canada.ORCID https://orcid.org/0000-0001-5005-4144
Francois Gros-LouisRegenerative Medicine Division, CHU de Québec-Université Laval, Canada.ORCID https://orcid.org/0000-0003-3825-4885
Manon LeclercDepartement of Medicine, Université Laval, Québec, Canada.ORCID https://orcid.org/0009-0009-5958-6599
Nicolas DupreDepartement of Medicine, Université Laval, Québec, Canada.ORCID https://orcid.org/0000-0001-7270-6115

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder that predisposes affected individuals to benign and malignant tumors throughout their lifetime. Early detection of those lesions is critical for effective management. PET/CT with Methods: In this retrospective observational study, clinical data were collected from medical records, including sex, age, family history, clinical manifestations, and tumor diagnosis. Data on imaging and diagnostic modalities that led to the diagnosis of NF1-related tumors or other malignant and potentially malignant tumors were collected. These modalities included Results: A total of 79 adult patients with NF1 were included in this study, comprising 29 male and 50 female patients, all of whom had received an NF1 diagnosis. Of these, 51 patients (64.6%) underwent a Discussion: In this cohort of 79 adult patients with NF1,

Identifiers

PMID41878223
PMCPMC13007358

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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.