ArticleJournal of inherited metabolic disease1992
Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresis.
Article in Journal of inherited metabolic disease, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled 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.
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.
Who cites it
15 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Guidelines on the Use of Therapeutic Apheresis in Clinical Practice-Evidence-Based Approach From the Writing Committee of the American Society for Apheresis: The Tenth Special Issue.Journal of clinical apheresis · 2026Guideline
- Diagnosis and Metabolic Management of Adult Refsum Disease: Guidance From the Medical and Scientific Committee of Global DARE (Defeat Adult Refsum Everywhere).Journal of inherited metabolic disease · 2026Guideline
- A brief history of the human liver peroxisome.Histochemistry and cell biology · 2026Review
- The neurology of rhizomelic chondrodysplasia punctata.Orphanet journal of rare diseases · 2013Article
- Identification of PEX7 as the second gene involved in Refsum disease.American journal of human genetics · 2003Article
- Mutational spectrum in the PEX7 gene and functional analysis of mutant alleles in 78 patients with rhizomelic chondrodysplasia punctata type 1.American journal of human genetics · 2002Article
- Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.American journal of human genetics · 2001Article
- Peroxisomal disorders: clinical, biochemical, and molecular aspects.Neurochemical research · 1999Review
- Molecular basis of rhizomelic chondrodysplasia punctata type I: high frequency of the Leu-292 stop mutation in 38 patients.Journal of inherited metabolic disease · 1998Article
- Immunocytochemical localization of peroxisomal proteins in human liver and kidney.Journal of inherited metabolic disease · 1995Article
- Diagnostic work-up of a peroxisomal patient.Journal of inherited metabolic disease · 1995Review
- Practical guide for morphometry of human peroxisomes on electron micrographs.Journal of inherited metabolic disease · 1995Review
- Chondrodysplasia punctata with a mild clinical course.Journal of inherited metabolic disease · 1994Article
- Peroxisomal disorders: a review.Journal of inherited metabolic disease · 1994Review
- Clinical and biochemical characteristics of peroxisomal disorders: an update.European journal of pediatrics · 1994Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
1405474What OpenQuestion holds
Registered trials
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.