Evidence map›Paper›PMID 40062579›Full record

ArticleMovement disorders clinical practice2025

FIC Domain Protein Adenylyltransferase (FICD)-Related Complex Hereditary Spastic Paraplegia with Diabetes Mellitus.

Adriana P Rebelo, Adel Alawwadh, Ali Hakami, Vanja Viric, Saeed Alshahrani, Marija Brankovic, Zorica Stevic, Stephan Zuchner, Abdulaziz Al-Shehri, Stojan Peric

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Movement disorders clinical practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Inhibition of FicD-mediated AMPylation and deAMPylation by isoprenoid diphosphates.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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

10 authors.

Adriana P RebeloDr. John T. Macdonald Foundation, Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, USA.ORCID https://orcid.org/0000-0001-5669-7415
Adel AlawwadhDepartment of Pediatrics, Khamis Mushait Maternity and Children Hospital, Abha, Saudi Arabia.
Ali HakamiDepartment of Pediatrics, Khamis Mushait Maternity and Children Hospital, Abha, Saudi Arabia.
Vanja ViricUniversity Clinical Center of Serbia-Neurology Clinic, University of Belgrade, Faculty of Medicine, Belgrade, Serbia.
Saeed AlshahraniDepartment of Pediatrics, Khamis Mushait Maternity and Children Hospital, Abha, Saudi Arabia.
Marija BrankovicUniversity Clinical Center of Serbia-Neurology Clinic, University of Belgrade, Faculty of Medicine, Belgrade, Serbia.
Zorica StevicUniversity Clinical Center of Serbia-Neurology Clinic, University of Belgrade, Faculty of Medicine, Belgrade, Serbia.
Stephan ZuchnerDr. John T. Macdonald Foundation, Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, USA.
Abdulaziz Al-ShehriDepartment of Child Health, Child Neurology, King Khalid University Medical City, Abha, Saudi Arabia.ORCID https://orcid.org/0000-0001-6894-7856
Stojan PericUniversity Clinical Center of Serbia-Neurology Clinic, University of Belgrade, Faculty of Medicine, Belgrade, Serbia.

Funding

GENOME STUDIES IN HEREDITARY SPASTIC PARAPLEGIA - beyond the exomeR01NS072248 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Stephan Zuchner · 2011 to 2026
$9.2M
NINDS NIH HHS R01 NS072248
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AMPylationBiPdiabetesFICDhereditary spastic paraplegia

Identifiers

PMID40062579
PMCPMC12371442

What OpenQuestion holds

Textmetadata
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.