Evidence map›Paper›PMID 35281597›Full record

ArticleBioMed research international2022

Novel

Ahmed Bouhouche, Yasmin Tabache, Omar Askander, Hicham Charoute, Nada Mesnaoui, Lamiae Belayachi, Naima El Hafidi, Houyam Hardizi, Elmostafa El Fahime, Naima Erreimi and 4 more

Open access · hybridAbstract readCase Reports
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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

14 authors at 4 institutions in 1 country.

Ahmed BouhoucheResearch Team in Neurology and Neurogenetics, Genomics Center of Human Pathologies, Medical School and Pharmacy, Mohammed V University in Rabat, Morocco.ORCID https://orcid.org/0000-0001-5279-8649
Yasmin TabacheDepartment of Pediatrics, Abulcasis International University of Health Sciences, Rabat, Morocco.
Omar AskanderResearch Genetics Center of the Cheikh Zaid Foundation, Abulcasis International University of Health Sciences, Rabat, Morocco.
Hicham CharouteResearch Unit of Epidemiology, Biostatistics and Bioinformatics, Institut Pasteur du Maroc, Casablanca, Morocco.ORCID https://orcid.org/0000-0002-9338-6744
Nada MesnaouiCentre of childhood Care and Prevention, Cheikh Zaid International Universitary Hospital, Rabat, Morocco.
Lamiae BelayachiResearch Genetics Center of the Cheikh Zaid Foundation, Abulcasis International University of Health Sciences, Rabat, Morocco.
Naima El HafidiDepartment of Pediatric Children Hospital, Medical School and Pharmacy, Mohammed V University in Rabat, Morocco.
Houyam HardiziResearch Genetics Center of the Cheikh Zaid Foundation, Abulcasis International University of Health Sciences, Rabat, Morocco.
Elmostafa El FahimeMolecular Biology and Functional Genomics Platform, National Center for Scientific and Technical Research, Rabat, Morocco.ORCID https://orcid.org/0000-0001-7812-0641
Naima ErreimiDepartment of Pediatrics, Abulcasis International University of Health Sciences, Rabat, Morocco.
Abdelhamid BarakatLaboratory of Genomics and Human Genetics, Institut Pasteur du Maroc, Casablanca, Morocco.ORCID https://orcid.org/0000-0002-6239-0281
Mohammed KhattabDepartment of Pediatrics, Abulcasis International University of Health Sciences, Rabat, Morocco.
Fouad SeghrouchniLaboratory of the Cellular Immunology, Institut National d'Hygiène, Rabat, Morocco.ORCID https://orcid.org/0000-0001-9935-2580
Amine El HassaniDepartment of Pediatrics, Abulcasis International University of Health Sciences, Rabat, Morocco.
Hôpital Universitaire International Cheikh Khalifa · MAMohammed V University · MAInstitut Pasteur du Maroc · MAInstitut National d'Hygiène du Maroc · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark features of the disease. It results from mutations in the integrin

Indexed as

CD18 AntigensLeukocyte-Adhesion Deficiency SyndromeHumansInfantMaleMutationPhenotypeCD18 Antigens

Identifiers

PMID35281597
PMCPMC8913115
OpenAlexW4214940146

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.