Evidence map›Paper›PMID 29977761›Full record

ArticleRespiratory medicine case reports2018

Alpha1 antitrypsin deficiency due to an homozygous PI* Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expression.

Zineb Jouhadi, Marie Francoise Odou, Farid Zerimech, Ahmed Aziz Bousfiha, Nabiha Mikou, Nicole Porchet, Michel Crepin, Jilali Najib, Malika Balduyck

Open access · goldAbstract readCase Reports
In one paragraph

Article in Respiratory medicine case reports, 2018. 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
0.3field-weighted citation impact, top 47% 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, 5 citations in OpenAlex.

  1. The phenotypic state of biallelicERJ open research · 2025
    Article
  2. Variants ofTherapeutic advances in chronic disease · 2021
    Review
  3. Advances in Alpha-1 Antitrypsin Gene Therapy.American journal of respiratory cell and molecular biology · 2020
    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

9 authors at 4 institutions in 2 countries.

Zineb JouhadiPediatric Infectious Diseases Department, Faculty of Medicine and Pharmacy Hassan II University, Casablanca, Morocco.
Marie Francoise OdouCHU Lille, Service de Biochimie et Biologie Moléculaire Hormonologie, Métabolisme-Nutrition, Oncologie, F-59000 Lille, France.
Farid ZerimechCHU Lille, Service de Biochimie et Biologie Moléculaire Hormonologie, Métabolisme-Nutrition, Oncologie, F-59000 Lille, France.
Ahmed Aziz BousfihaPediatric Infectious Diseases Department, Faculty of Medicine and Pharmacy Hassan II University, Casablanca, Morocco.
Nabiha MikouPediatric Rheumatology Department, Faculty of Medicine and Pharmacy Hassan II University, Casablanca, Morocco.
Nicole PorchetCHU Lille, Service de Biochimie et Biologie Moléculaire Hormonologie, Métabolisme-Nutrition, Oncologie, F-59000 Lille, France.
Michel CrepinCHU Lille, Service de Biochimie et Biologie Moléculaire Hormonologie, Métabolisme-Nutrition, Oncologie, F-59000 Lille, France.
Jilali NajibPediatric Infectious Diseases Department, Faculty of Medicine and Pharmacy Hassan II University, Casablanca, Morocco.
Malika BalduyckCHU Lille, Service de Biochimie et Biologie Moléculaire Hormonologie, Métabolisme-Nutrition, Oncologie, F-59000 Lille, France.
University of Hassan II Casablanca · MACentre Hospitalier Universitaire de Lille · FRUniversité de Lille · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alpha-1 antitrypsin deficiency is an autosomal, codominant disorder caused by mutations of the

Indexed as

Alpha-1 antitrypsin deficiencyBronchiectasisNull mutationPanniculitisSERPINA1 genotyping

Identifiers

PMID29977761
PMCPMC6010612
OpenAlexW2797886344

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.