Evidence map›Paper›PMID 39597062›Full record

ArticleMedicina (Kaunas, Lithuania)2024

Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome in Vietnamese Patients.

Khanh Ngoc Nguyen, Van Khanh Tran, Ngoc Lan Nguyen, Thi Bich Ngoc Can, Thi Kim Giang Dang, Thu Ha Nguyen, Thi Thanh Mai Do, Le Thi Phuong, Thinh Huy Tran, Thanh Van Ta and 2 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Mitochondrial HMG-CoA Synthase Deficiency in Vietnamese Patients.International journal of molecular sciences · 2025
    Article
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

12 authors.

Khanh Ngoc NguyenCenter of Endocrinology, Metabolism, Genetic/Genomics and Molecular Therapy, Vietnam National Children's Hospital, 18/879 La Thanh, Dong Da, Hanoi 11512, Vietnam.
Van Khanh TranCenter for Gene and Protein Research, Hanoi Medical University, 1st Ton That Tung Street, Hanoi 11521, Vietnam.
Ngoc Lan NguyenCenter for Gene and Protein Research, Hanoi Medical University, 1st Ton That Tung Street, Hanoi 11521, Vietnam.
Thi Bich Ngoc CanCenter of Endocrinology, Metabolism, Genetic/Genomics and Molecular Therapy, Vietnam National Children's Hospital, 18/879 La Thanh, Dong Da, Hanoi 11512, Vietnam.
Thi Kim Giang DangCenter of Endocrinology, Metabolism, Genetic/Genomics and Molecular Therapy, Vietnam National Children's Hospital, 18/879 La Thanh, Dong Da, Hanoi 11512, Vietnam.
Thu Ha NguyenCenter of Endocrinology, Metabolism, Genetic/Genomics and Molecular Therapy, Vietnam National Children's Hospital, 18/879 La Thanh, Dong Da, Hanoi 11512, Vietnam.
Thi Thanh Mai DoCenter of Endocrinology, Metabolism, Genetic/Genomics and Molecular Therapy, Vietnam National Children's Hospital, 18/879 La Thanh, Dong Da, Hanoi 11512, Vietnam.
Le Thi PhuongCenter for Gene and Protein Research, Hanoi Medical University, 1st Ton That Tung Street, Hanoi 11521, Vietnam.ORCID 0009-0000-9557-9868
Thinh Huy TranBiochemistry Department, Hanoi Medical University, 1st Ton That Tung Street, Hanoi 11521, Vietnam.
Thanh Van TaBiochemistry Department, Hanoi Medical University, 1st Ton That Tung Street, Hanoi 11521, Vietnam.ORCID 0000-0002-2776-4911
Nguyen Huu TuHanoi Medical Univerity Hospital, Hanoi Medical University, 1st Ton That Tung Street, Hanoi 11521, Vietnam.
Chi Dung VuCenter of Endocrinology, Metabolism, Genetic/Genomics and Molecular Therapy, Vietnam National Children's Hospital, 18/879 La Thanh, Dong Da, Hanoi 11512, Vietnam.ORCID 0009-0007-0418-2613

Funding

Vietnam Ministry of Science and Technology ĐTĐL.CN.133/21
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HyperammonemiaUrea Cycle Disorders, InbornChild, PreschoolCitrullineFemaleHumansInfantInfant, NewbornMaleMitochondrial Membrane Transport ProteinsOrnithineProspective StudiesRetrospective StudiesSoutheast Asian PeopleVietnamCitrullinehomocitrullineMitochondrial Membrane Transport ProteinsOrnithineSLC25A15 protein, humanHHH syndromep.Arg179*p.Met137Cysfs*10p.Phe188delSLC25A15 variantVietnamese patients

Identifiers

PMID39597062
PMCPMC11596723

What OpenQuestion holds

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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.