Evidence map›Paper›PMID 35535100›Full record

ArticleJournal of clinical and experimental hepatology

Living-Donor Liver Transplantation for Late-Onset Lysosomal Acid Lipase Deficiency.

Somashekara H Ramakrishna, Mohan B Kasala, Karnan Perumal, Selvakumar Malleeswaran, Rajanikanth V Patcha, Joy Varghese

Open access · bronzeAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical and experimental hepatology. 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
0.3field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 1 country.

Somashekara H RamakrishnaConsultant Pediatric Hepatologist, Gleneagles Global Health City, Perumbakkam, Chennai, India.
Mohan B KasalaDepartment of Pediatric Intensive Care, Gleneagles Global Health City, Perumbakkam, Chennai, India.
Karnan PerumalDepartment of Pediatric Intensive Care, Gleneagles Global Health City, Perumbakkam, Chennai, India.
Selvakumar MalleeswaranLiver Anesthesia and Critical Care, Gleneagles Global Health City, Perumbakkam, Chennai, India.
Rajanikanth V PatchaDepartment of Liver Transplant and Hepatopancreaticobiliary Surgery, Gleneagles Global Health City, Perumbakkam, Chennai, India.
Joy VargheseDepartment of Hepatology and Liver Transplant, Gleneagles Global Health City, Perumbakkam, Chennai, India.
Global Hospitals · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Late-onset liposomal acid lipase deficiency (LAL deficiency), previously known as Cholesteryl ester storage disease (CESD) is a rare genetic lysosomal storage disorder caused by deficiency of lysosomal acid lipase (LAL) due to mutations in the

Indexed as

CE, Cholesteryl esterCESDCESD, Cholesteryl ester storage diseaseCT, Computerized tomographyESLD, End-stage liver diseaseGRWR, Graft to recipient weightHDL, High-density lipoproteinLAL-D, Lysosomal acid lipase deficiencyLAL, Lysosomal acid lipaselate-onset LAL deficiencyLDL, Low-density lipoproteinLDLTLDLT, Living-donor liverliver transplantationLT, Liver transplantNGS, Next-generation sequencingPAS-D, Periodic acid-Schiff-diastasesebelipase alfaWD, Wolman disease

Identifiers

PMID35535100
PMCPMC9077196
OpenAlexW3178446143

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.