Observational studyInternational journal of molecular sciences2026
Hypokalemic Hypochloremic Metabolic Alkalosis in Cystic Fibrosis: A Retrospective Observational Study with Clinical Characterization,
Andressa Oliveira Peixoto, Larissa Ferreira Selicani, Camila Bento Safi, Daniela Souza Paiva Borgli, Adyléia Aparecida Dalbo Contrera Toro, Nathália Mariana Santos Sansone, Andrea de Melo Alexandre Fraga, Fernando Augusto Lima Marson, José Dirceu Ribeiro
Abstract readObservational StudyComparative Study
In one paragraphObservational study in International journal of molecular sciences, 2026. 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
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
9 authors.
Andressa Oliveira PeixotoPediatric Research Center, Faculty of Medical Sciences, University of Campinas (Unicamp-Universidade de Campinas), Campinas 13083-887, SP, Brazil.
Larissa Ferreira SelicaniFaculty of Medical Sciences, University of Sapucaí Valley (Univás-Universidade do Vale do Sapucaí), Pouso Alegre 37550-000, MG, Brazil.
Camila Bento SafiFaculty of Medical Sciences, Pontifical Catholic University of Campinas (PUC-Campinas-Pontifícia Universidade Católica de Campinas), Campinas 13086-900, SP, Brazil.ORCID 0009-0000-4192-8495 Daniela Souza Paiva BorgliPediatric Research Center, Faculty of Medical Sciences, University of Campinas (Unicamp-Universidade de Campinas), Campinas 13083-887, SP, Brazil.
Adyléia Aparecida Dalbo Contrera ToroPediatric Research Center, Faculty of Medical Sciences, University of Campinas (Unicamp-Universidade de Campinas), Campinas 13083-887, SP, Brazil.
Nathália Mariana Santos SansoneLaboratory of Molecular Biology and Genetics, Postgraduate Program in Health Sciences and Postgraduate Program in Health Data Science, São Francisco University (USF-Universidade São Francisco), Bragança Paulista 12916-900, SP, Brazil.
Andrea de Melo Alexandre FragaPediatric Research Center, Faculty of Medical Sciences, University of Campinas (Unicamp-Universidade de Campinas), Campinas 13083-887, SP, Brazil.
Fernando Augusto Lima MarsonLaboratory of Molecular Biology and Genetics, Postgraduate Program in Health Sciences and Postgraduate Program in Health Data Science, São Francisco University (USF-Universidade São Francisco), Bragança Paulista 12916-900, SP, Brazil.ORCID 0000-0003-4955-4234 José Dirceu RibeiroPediatric Research Center, Faculty of Medical Sciences, University of Campinas (Unicamp-Universidade de Campinas), Campinas 13083-887, SP, Brazil.ORCID 0000-0002-3387-5642 Funding
Conselho Nacional de Desenvolvimento Científico e Tecnológico 300024/2025-8Conselho Nacional de Desenvolvimento Científico e Tecnológico 305906/2024-0
6 · The paper itselfAbstract
Cystic fibrosis is a genetic disorder caused by pathogenic variants in the Cystic Fibrosis Transmembrane Conductance Regulator (
Indexed as
AlkalosisCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorHypokalemiaAdolescentBrazilChildChild, PreschoolFemaleHumansInfantMaleMutationRetrospective StudiesCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorCFTR genotypecystic fibrosiselectrolyteshypokalemiametabolic alkalosisPseudo-Bartter syndrome
Identifiers
PMID42737565
PMCPMC13566040
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