Evidence map›Paper›PMID 30607525›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2019

A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient.

Mariano Oliva, Guglielmo Capaldo, Alessandra D'Amico, Davide Colavito, Andrea Elefante, Giulia Straccia, Lorenzo Ugga, Gianfranco Puoti

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2019. 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
0.7field-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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Rare Neurologic Diseases and Neurological Sciences: a report for the celebration of the 2020 Rare Diseases Day.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2020
    Article
  2. Basal ganglia calcifications (Fahr's syndrome): related conditions and clinical features.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Review
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

8 authors at 2 institutions in 1 country.

Mariano OlivaDipartimento di Scienze Mediche Chirurgiche Neurologiche Metaboliche e dell'Invecchiamento, Università degli studi della Campania Luigi Vanvitelli, P.zza Miraglia 2, 80138, Naples, Italy.
Guglielmo CapaldoDipartimento di Scienze Mediche Chirurgiche Neurologiche Metaboliche e dell'Invecchiamento, Università degli studi della Campania Luigi Vanvitelli, P.zza Miraglia 2, 80138, Naples, Italy.
Alessandra D'AmicoDipartimento di Scienze Biomediche Avanzate, Università degli Studi di Napoli Federico II, Via Pansini 5, 80131, Naples, Italy.
Davide ColavitoResearch & Innovation srl (R&I Genetics), C.so Stati Uniti 4 int. F, 35127, Padova, Italy.
Andrea ElefanteDipartimento di Scienze Biomediche Avanzate, Università degli Studi di Napoli Federico II, Via Pansini 5, 80131, Naples, Italy.
Giulia StracciaDipartimento di Scienze Mediche Chirurgiche Neurologiche Metaboliche e dell'Invecchiamento, Università degli studi della Campania Luigi Vanvitelli, P.zza Miraglia 2, 80138, Naples, Italy.
Lorenzo UggaDipartimento di Scienze Biomediche Avanzate, Università degli Studi di Napoli Federico II, Via Pansini 5, 80131, Naples, Italy.
Gianfranco PuotiDipartimento di Scienze Mediche Chirurgiche Neurologiche Metaboliche e dell'Invecchiamento, Università degli studi della Campania Luigi Vanvitelli, P.zza Miraglia 2, 80138, Naples, Italy. gianfranco.puoti@unicampania.it.ORCID http://orcid.org/0000-0002-6452-2321
University of Campania "Luigi Vanvitelli" · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationBrain DiseasesCalcinosisDiagnosis, DifferentialFemaleHumansMiddle AgedPedigreePhenotypeSodium-Phosphate Cotransporter Proteins, Type IIIUkraineSLC20A2 protein, humanSodium-Phosphate Cotransporter Proteins, Type III

Identifiers

PMID30607525
OpenAlexW2907693817

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.