[Hyperuricemia with cerebral paresis. Syndrome of a hereditary purine metabolic disorder]

Clicks: 351
ID: 114165
1967
Free PDF
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Star

Ranked #1 of 2 articles by views in helvetica paediatrica acta

Most read Least read

Bar heights use a square-root scale.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Sign in to mint
Abstract
[Hyperuricemia with cerebral paresis. Syndrome of a hereditary purine metabolic disorder]
Reference Key
h1967helvetica[hyperuricemia Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Manzke H;;
Journal helvetica paediatrica acta
Year 1967
DOI
DOI not found
URL
https://www.ncbi.nlm.nih.gov/pubmed/5590141
Keywords
National Center for Biotechnology Information NCBI NLM MEDLINE humans pubmed abstract nih national institutes of health national library of medicine male adolescent Child Infant preschool h manzke pedigree anemia pmid:5590141 macrocytic / complications cerebral palsy / complications* glycine / blood hyperlipidemias / complications metabolism inborn errors / complications* purines / metabolism* uremia / complications uric acid / blood*

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.