Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.

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

5 citing papers in PubMed, 24 citations in OpenAlex.

1. 17p duplicated Charcot-Marie-Tooth 1A: characteristics of a new population.Journal of neurology · 2005
   Article
2. A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease.Journal of neurology, neurosurgery, and psychiatry · 2004
   Article
3. Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients.Journal of neurology · 1995
   Article
4. Homozygous hypertrophic hereditary motor and sensory neuropathies.Italian journal of neurological sciences · 1994
   Article
5. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication.American journal of human genetics · 1993
   Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

9 authors at 1 institution in 1 country.

Funding

Abstract

PubMed holds no abstract for this paper.

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