ArticleJournal of inherited metabolic disease2000
Carbohydrate-deficient glycoprotein syndromes: the Italian experience.
Article in Journal of inherited metabolic disease, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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
6 citing papers in PubMed.
- A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation.Journal of neurology · 2015Article
- A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case report.Orphanet journal of rare diseases · 2010Article
- Cardiomyopathy in the congenital disorders of glycosylation (CDG): a case of late presentation and literature review.Journal of inherited metabolic disease · 2009Review
- The congenital disorders of glycosylation: a multifaceted group of syndromes.NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics · 2006Review
- Biochemical and molecular studies in 26 Spanish patients with congenital disorder of glycosylation type Ia.Journal of inherited metabolic disease · 2002Article
- High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency).American journal of human genetics · 2001Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
10896302What 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.