The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.

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

12 citing papers in PubMed.

1. Complementary roles of murine NaScientific reports · 2020
   Article
2. Gain-of-function mutation in SCN11A causes itch and affects neurogenic inflammation and muscle function in Scn11a+/L799P mice.PloS one · 2020
   Article
3. Hereditary Sensory and Autonomic Neuropathies: Adding More to the Classification.Current neurology and neuroscience reports · 2019
   Review
4. Identification of peptidomimetics as novel chemical probes modulating fibroblast growth factor 14 (FGF14) and voltage-gated sodium channel 1.6 (Nav1.6) protein-protein interactions.Bioorganic & medicinal chemistry letters · 2019
   Article
5. A disease mutation reveals a role for NaV1.9 in acute itch.The Journal of clinical investigation · 2018
   Article
6. NaV1.1 inhibition can reduce visceral hypersensitivity.JCI insight · 2018
   Article
7. Office-Based Anesthetic and Oral Surgical Management of a Child With Hereditary Sensory Autonomic Neuropathy Type IV: A Case Report.Anesthesia progress · 2018
   Article
8. Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.Journal of medical case reports · 2017
   Review
9. The influence of sodium on pathophysiology of multiple sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2017
   Review
10. Identification of Amino Acid Residues in Fibroblast Growth Factor 14 (FGF14) Required for Structure-Function Interactions with Voltage-gated Sodium Channel Nav1.6.The Journal of biological chemistry · 2016
    Article
11. Sisters with No Pain, No Tears: A Report of a New Variant of Hereditary Sensory and Autonomic Neuropathy (Type IX) Caused by a Novel SCN11A Mutation.Indian journal of dermatology
    Article
12. MrgprX1 Mediates Neuronal Excitability and Itch Through Tetrodotoxin-Resistant Sodium Channels.Itch (Philadelphia, Pa.)
    Article

Corrections and comments

• Erratum for
  The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.2015

Authors and funding

5 authors.

Funding

Abstract

PubMed holds no abstract for this paper.