Evidence map›Paper›PMID 30754660›Full record

ArticleCells2019

Nevoid Basal Cell Carcinoma Syndrome:

Maria Florencia Martinez, Maria Vanesa Romano, Alfredo Pedro Martinez, Abel González, Carolina Muchnik, Fernando Miguel Stengel, Luis Daniel Mazzuoccolo, Pablo Javier Azurmendi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Navigating the Molecular Signaling: Deciphering Cancer Stem Cell Self-Renewal Pathways.International journal of molecular and cellular medicine · 2025
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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 3 institutions in 1 country.

Maria Florencia MartinezLaboratorio de Nefrología Experimental y Bioquímica Molecular, Instituto de Investigaciones Médicas "Alfredo Lanari", Facultad de Medicina, Universidad de Buenos Aires, 1427 Buenos Aires, Argentina. martinez.mflorencia@gmail.com.
Maria Vanesa RomanoDepartamento de Análisis Clínicos, Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno", 1431 Buenos Aires, Argentina. vromano@cemic.edu.ar.
Alfredo Pedro MartinezDepartamento de Análisis Clínicos, Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno", 1431 Buenos Aires, Argentina. amartinez@cemic.edu.ar.
Abel GonzálezUnidad de Cirugía de MOHS, Departamento de Cirugía de Cabeza y Cuello, Instituto de Oncología "Ángel H. Roffo", Facultad de Medicina, Universidad de Buenos Aires, 1408 Buenos Aires, Argentina. abelgo@gmail.com.
Carolina MuchnikLaboratorio de Nefrología Experimental y Bioquímica Molecular, Instituto de Investigaciones Médicas "Alfredo Lanari", Facultad de Medicina, Universidad de Buenos Aires, 1427 Buenos Aires, Argentina. caromuch@hotmail.com.ORCID 0000-0002-1542-3706
Fernando Miguel StengelBuenos Aires Skin, 1055 Buenos Aires, Argentina. fernando@stengeldermato.com.ar.
Luis Daniel MazzuoccoloServicio de Dermatología, Hospital Interzonal General de Agudos "Eva Perón", 1650 Gral. San Martin, Argentina. luis.mazzuoccolo@hospitalitaliano.org.ar.ORCID 0000-0002-6315-7916
Pablo Javier AzurmendiLaboratorio de Nefrología Experimental y Bioquímica Molecular, Instituto de Investigaciones Médicas "Alfredo Lanari", Facultad de Medicina, Universidad de Buenos Aires, 1427 Buenos Aires, Argentina. azurmendi.pablo@lanari.uba.ar.ORCID 0000-0001-7787-5882
Universidad de Buenos Aires · ARCentro de Educación Médica e Investigaciones Clínicas Norberto Quirno · ARNational University of General San Martín · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by multiple basal cell carcinomas (BCC), mainly caused by

Indexed as

Gene Expression Regulation, NeoplasticSignal TransductionAdolescentAdultAgedAllelesArgentinaBasal Cell Nevus SyndromeChildFemaleHedgehog ProteinsHumansMaleMiddle AgedMutationPatched-1 ReceptorHedgehog ProteinsPatched-1 ReceptorPTCH1 protein, humanRNA, Messengerbasal cell carcinomaGorlin–Goltz syndromeHedgehog pathwayPTCH1 mutation

Identifiers

PMID30754660
PMCPMC6406887
OpenAlexW2913486017

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.