Evidence map›Paper›PMID 25398234›Full record

ArticleBrain : a journal of neurology2015

Reply: Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.

Niccolo E Mencacci, Alan M Pittman, Ioannis U Isaias, John Hardy, Stephan Klebe, Kailash P Bhatia, Nicholas W Wood

Open access · hybridAbstract 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Niccolo E Mencacci1 Department of Molecular Neuroscience, UCL Institute of Neurology, London WC1N 3BG, UK 2 IRCCS Istituto Auxologico Italiano, Department of Neurology and Laboratory of Neuroscience - Department of Pathophysiology and Transplantation, 'Dino Ferrari' Centre, Universita` degli Studi di Milano, 20149 Milan, Italy.
Alan M Pittman1 Department of Molecular Neuroscience, UCL Institute of Neurology, London WC1N 3BG, UK 3 Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London WC1N 3BG, UK.
Ioannis U Isaias4 Department of Neurology, University Hospital, 97080 Würzburg, Germany 5 Parkinson Institute, Istituti Clinici di Perfezionamento, 20126 Milan, Italy.
John Hardy1 Department of Molecular Neuroscience, UCL Institute of Neurology, London WC1N 3BG, UK 3 Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London WC1N 3BG, UK.
Stephan Klebe4 Department of Neurology, University Hospital, 97080 Würzburg, Germany.
Kailash P Bhatia6 Sobell Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, London WC1N 3BG, UK.
Nicholas W Wood1 Department of Molecular Neuroscience, UCL Institute of Neurology, London WC1N 3BG, UK n.wood@ucl.ac.uk.
University College London · GBUniversitätsklinikum Würzburg · DEIRCCS Istituto Auxologico Italiano · ITSobell House · GB

Funding

Medical Research Council MC_G0901330Medical Research Council MC_PC_09003Medical Research Council MR/L501554/1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HeterozygoteFemaleGTP CyclohydrolaseHumansMaleMutationParkinson DiseaseGTP Cyclohydrolase

Identifiers

PMID25398234
PMCPMC4407186
OpenAlexW2165231572

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.