Evidence map›Paper›PMID 26862418›Full record

ArticleClinical case reports2016

Mild phenotype in an adult male with X-linked adrenoleukodystrophy - case report.

Morten A Horn, Karin B M Mikaelsen, Sacha Ferdinandusse, Ellen Jørum, Svein I Mellgren, Lars Retterstøl, Ronald J A Wanders, Chantal M E Tallaksen

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical case reports, 2016. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

Morten A HornDepartment of Neurology Oslo University Hospital PO Box 4956 Nydalen Oslo N-0424 Norway; Department of Neurology Faculty of Medicine University of Oslo PO Box 1078 Blindern Oslo N-0316 Norway.
Karin B M MikaelsenDepartment of Neurology Molde Hospital HF Parkveien 84 Molde N-6407 Norway.
Sacha FerdinandusseLaboratory Genetic Metabolic Diseases Department of Clinical Chemistry Academic Medical Centre Meibergdreef 9 Amsterdam 1105 AZ The Netherlands.
Ellen JørumDepartment of Neurology Oslo University Hospital PO Box 4956 Nydalen Oslo N-0424 Norway; Department of Neurology Faculty of Medicine University of Oslo PO Box 1078 Blindern Oslo N-0316 Norway.
Svein I MellgrenDepartment of Neurology University Hospital of Northern Norway Tromsø N-9038 Norway; Department of Clinical Medicine UiT the Arctic University of Norway PO Box 6050 Langnes N-9037 Tromsø Norway.
Lars RetterstølDepartment of Medical Genetics Oslo University Hospital N-0424 Oslo Norway.
Ronald J A WandersLaboratory Genetic Metabolic Diseases Department of Clinical Chemistry Academic Medical Centre Meibergdreef 9 Amsterdam 1105 AZ The Netherlands.
Chantal M E TallaksenDepartment of Neurology Oslo University Hospital PO Box 4956 Nydalen Oslo N-0424 Norway; Department of Neurology Faculty of Medicine University of Oslo PO Box 1078 Blindern Oslo N-0316 Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked adrenoleukodystrophy may present with a deceptively mild phenotype, even in adult males. Tight collaboration between clinicians, geneticists, biochemists, and other specialists is increasingly required for clarification of diagnosis in cases with atypical presentation.

Indexed as

AdrenomyeloneuropathyleukodystrophymyelopathyParkinson's diseasephenotypeX‐linked adrenoleukodystrophy

Identifiers

PMID26862418
PMCPMC4736514

What OpenQuestion holds

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Registered trials

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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.