Evidence map›Paper›PMID 31989346›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2020

Awareness of rare and genetic neurological diseases among italian neurologist. A national survey.

Michelangelo Mancuso, Massimiliano Filosto, Costanza Lamperti, Olimpia Musumeci, Filippo M Santorelli, Serenella Servidei, Enza M Valente, Massimo Zeviani, Gianluigi Mancardi, Gioacchino Tedeschi and 1 more

Abstract read
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In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Rare disease education in Europe and beyond: time to act.Orphanet journal of rare diseases · 2022
    Article
  3. 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

11 authors at 11 institutions in 1 country.

Michelangelo MancusoDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy. mancusomichelangelo@gmail.com.ORCID http://orcid.org/0000-0003-2738-8562
Massimiliano FilostoUnit of Neurology, ASST "Spedali Civili" and University of Brescia, Brescia, Italy.
Costanza LampertiUO Medical Genetics and Neurogentics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Olimpia MusumeciDepartment of Clinical and Experimental Medicine Unit of Neurological and Neuromuscular Disorders, University of Messina, Messina, Italy.
Filippo M SantorelliMolecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, IRCCS Stella Maris Foundation, 56128, Pisa, Italy.
Serenella ServideiUOC Neurofisiopatologia Fondazione Policlinico Universitario, A. Gemelli IRCCS, Istituto di Neurologia Università Cattolica del Sacro Cuore, Roma, Italy.
Enza M ValenteDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Massimo ZevianiDepartment of Neuroscience, University of Padua, Padua, Italy.
Gianluigi MancardiDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health and Neuromotor Department, University of Genova and IRCCS ICS Maugeri, Genoa and Pavia, Italy.
Gioacchino TedeschiDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
Antonio FedericoDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy.
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITFondazione Stella Maris · ITIstituti Clinici Scientifici Maugeri · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Messina · ITUniversity of Padua · ITUniversity of Pavia · ITUniversity of Pisa · ITUniversity of Siena · IT

Funding

Medical Research Council MC_EX_MR/P007031/1Medical Research Council MC_UP_1002/1Medical Research Council MC_UU_00015/5MRF_ MRF-155-0001-S-MARTIMRF_ MRF-155-0002-RG-ZEVIAMRF_ MRF-155-0005-RG-ZEVI-C0784
6 · The paper itself

Abstract

Rare neurological diseases (RNDs) are a heterogeneous group of disorders mainly affecting the central and peripheral nervous systems, representing almost 50% of all rare diseases; this explains why neurologists are very often involved in their diagnosis, treatment and research. The purpose of this study was to quantitatively describe the awareness of RNDs among the neurological community of the Italian Society of Neurology (SIN). A survey of the Italian Neurogenetics and Rare diseases group of the SIN, similar to what was submitted to the members of the EAN Task Force on Rare Neurologic Diseases and to EAN Panels Scientific Committee Management Groups, was launched in January 2019 in order to verify the specific Italian situations and possibly the regional differences. Answers were collected online. We observed that Italian Members of the SIN Neurogenetics and Rare Neurologic Diseases Scientific Group are well aware of the burden posed by RNDs but at the national and regional level, the relative awareness is sketchy and disparate. Although many national initiatives have been undertaken to facilitate the diagnosis and management in Italy, our survey reveals that much works has to be done in supporting RNDs patients, including a deeper collaboration between politics, universities and all stakeholders in the field.

Indexed as

Attitude of Health PersonnelHealth Knowledge, Attitudes, PracticeNervous System DiseasesRare DiseasesAdultCross-Sectional StudiesHealth Care SurveysHumansItalyMiddle AgedNeurologistsPractice Patterns, Physicians'Societies, MedicalAwarenessNational surveyRare neurological diseases

Identifiers

PMID31989346
OpenAlexW3003618762

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.