Syndromes with lissencephaly.

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

11 citing papers in PubMed.

1. Understanding the Molecular Basis of Miller-Dieker Syndrome.International journal of molecular sciences · 2025
   Review
2. Multi-Omics Approach Reveals Genes and Pathways Affected in Miller-Dieker Syndrome.Molecular neurobiology · 2025
   Article
3. Journal of the American Heart Association · 2023
   Article
4. Acute Bowel Ischemia in a Premature Neonate with Miller-Dieker Syndrome and Anomalous Right Coronary Artery From the Pulmonary Artery.Pediatric annals · 2023
   Review
5. Fetal Brain Development: Regulating Processes and Related Malformations.Life (Basel, Switzerland) · 2022
   Review
6. Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A).Journal of neuropathology and experimental neurology · 2020
   Article
7. Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3.Frontiers in genetics · 2018
   Review
8. Hereditary lissencephaly and cerebellar hypoplasia in Churra lambs.BMC veterinary research · 2013
   Article
9. Hippocampal abnormalities and enhanced excitability in a murine model of human lissencephaly.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000
   Article
10. Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation.Journal of medical genetics · 1998
    Article
11. Recurrence risks in mental retardation.Journal of medical genetics · 1998
    Review

Corrections and comments

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

Authors and funding

2 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as