Evidence map›Paper›PMID 25146916›Full record

ArticleBrain : a journal of neurology2015

'Behr syndrome' with OPA1 compound heterozygote mutations.

Valerio Carelli, Mario Sabatelli, Rosalba Carrozzo, Teresa Rizza, Simone Schimpf, Bernd Wissinger, Claudia Zanna, Michela Rugolo, Chiara La Morgia, Leonardo Caporali and 5 more

Abstract readLetterComment
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain : a journal of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Review
  2. Polyunsaturated fatty acid metabolism in the retinal pigment epithelium and its association with outer retinal disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Mitochondrial Retinopathies.International journal of molecular sciences · 2021
    Review
  14. Genes · 2021
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Valerio Carelli1 IRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy 2 Neurology Unit, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy valerio.carelli@unibo.it ebertini@tin.it.
Mario Sabatelli3 Institute of Neurology, Catholic University, Rome, Italy.
Rosalba Carrozzo4 Laboratory of Molecular Medicine, Research Children's Hospital 'Bambino Gesù', Rome, Italy.
Teresa Rizza4 Laboratory of Molecular Medicine, Research Children's Hospital 'Bambino Gesù', Rome, Italy.
Simone Schimpf5 Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, Germany.
Bernd Wissinger5 Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, Germany.
Claudia Zanna2 Neurology Unit, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy 6 Department of Pharmacy and Biotechnology (FABIT), University of Bologna, Bologna, Italy.
Michela Rugolo6 Department of Pharmacy and Biotechnology (FABIT), University of Bologna, Bologna, Italy.
Chiara La Morgia1 IRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy 2 Neurology Unit, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Leonardo Caporali1 IRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Michele Carbonelli7 Studio Oculistico D'Azeglio, Bologna, Italy.
Piero Barboni7 Studio Oculistico D'Azeglio, Bologna, Italy.
Caterina Tonon8 Functional MR Unit, Policlinico S. Orsola-Malpighi, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Raffaele Lodi8 Functional MR Unit, Policlinico S. Orsola-Malpighi, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Enrico Bertini4 Laboratory of Molecular Medicine, Research Children's Hospital 'Bambino Gesù', Rome, Italy valerio.carelli@unibo.it ebertini@tin.it.

Funding

Telethon GGP06233
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Central Nervous System DiseasesFemaleGTP PhosphohydrolasesHumansMaleOptic Atrophy, Autosomal DominantGTP Phosphohydrolases

Identifiers

PMID25146916
PMCPMC4441076

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.