Evidence map›Paper›PMID 36539614›Full record

ArticleAnnals of hematology2023

GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families.

Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Annals of hematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Serena BarozziMedicina Generale 1, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.ORCID 0000-0002-5622-739X
Alessandro PecciMedicina Generale 1, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.ORCID 0000-0001-9202-7013
Maddalena MarinoniMaternal and Child Department, F. Del Ponte Hospital, Varese, Italy.
Giorgia FontanaInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.ORCID 0000-0001-7268-4104
Melania Eva ZanchettaInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.
Patrizia NorisDepartment of Internal Medicine, University of Pavia, Pavia, Italy.ORCID 0000-0002-5035-3707
Anna SavoiaDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy. anna.savoia@univr.it.ORCID 0000-0002-2407-2696
Michela FaleschiniInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.ORCID 0000-0001-5147-3164

Funding

Fondazione Telethon GGP17106Italian Ministry of Health RC-2019-08068819Italian Ministry of Health RC 28/2022
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Bernard-Soulier SyndromePlatelet Glycoprotein GPIb-IX ComplexBlood PlateletsHumansItalyMutationadhesion receptorPlatelet Glycoprotein GPIb-IX Complex

Identifiers

PMID36539614

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.