Evidence map›Paper›PMID 39502851›Full record

ArticleJournal of pediatric genetics2024

Neonatal Onset Distal Renal Tubular Acidosis: Description of Two Novel Variants on the

Marita Antoniadi, Dimitra Lambrou, Fani Mylona, Lina Florentin, Chrysanthi Bili, Constantinos J Stefanidis, Stavroula Kostaridou

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of pediatric genetics, 2024. 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

7 authors.

Marita AntoniadiPediatric Department, Penteli Children's Hospital, Athens, Greece.ORCID 0000-0002-5629-9916
Dimitra LambrouPediatric Department, Penteli Children's Hospital, Athens, Greece.
Fani MylonaPediatric Department, Penteli Children's Hospital, Athens, Greece.
Lina FlorentinAlfaLab Genetics and Genomics Center Athens, Athens, Greece.
Chrysanthi BiliAlfaLab Genetics and Genomics Center Athens, Athens, Greece.
Constantinos J StefanidisMitera Children's Hospital, Athens, Greece.
Stavroula KostaridouPediatric Department, Penteli Children's Hospital, Athens, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Distal renal tubular acidosis (dRTA) is an extremely rare disease that affects the distal tubule's ability to excrete proton cations, acidify urine, and maintain the acid-base balance. The clinical presentation of dRTA typically includes normal anion gap metabolic acidosis with decreased serum bicarbonate levels, hypokalemia, hypercalcemia, nephrocalcinosis, and alkaline urine. Hereditary causes of dRTA include pathogenic variants in

Indexed as

ATP6V0A4dRTAfailure to thrivehypokalemianeonatal

Identifiers

PMID39502851
PMCPMC11534435

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.