Evidence map›Paper›PMID 36833327›Full record

SynthesisGenes2023

Concomitant Calcium Channelopathies Involving

Donna Schaare, Sara M Sarasua, Laina Lusk, Shridhar Parthasarathy, Liangjiang Wang, Ingo Helbig, Luigi Boccuto

Open access · goldAbstract readSystematic ReviewCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Synthesis in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. A Longitudinal Exploration ofNeurology. Genetics · 2025
    Review
  2. "Living with"Frontiers in neurology · 2024
    Article
  3. Developing a pathway to clinical trials forTherapeutic advances in rare disease
    Review
4 · The record

Corrections and comments

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

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Donna SchaarePh.D. Program in Healthcare Genetics and Genomics, School of Nursing, College of Behavioral, Social and Health Sciences, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-1132-3097
Sara M SarasuaPh.D. Program in Healthcare Genetics and Genomics, School of Nursing, College of Behavioral, Social and Health Sciences, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-1625-7404
Laina LuskDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Shridhar ParthasarathyDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Liangjiang WangDepartment of Genetics and Biochemistry, College of Science, Clemson University, Clemson, SC 29634, USA.
Ingo HelbigDepartment of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Luigi BoccutoPh.D. Program in Healthcare Genetics and Genomics, School of Nursing, College of Behavioral, Social and Health Sciences, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0003-2017-4270
Clemson University · USChildren's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcium channels are an integral component in maintaining cellular function. Alterations may lead to channelopathies, primarily manifested in the central nervous system. This study describes the clinical and genetic features of a unique 12-year-old boy harboring two congenital calcium channelopathies, involving the

Indexed as

ChannelopathiesMigraine with AuraCalciumCalcium ChannelsCalcium Channels, L-TypeCalcium Channels, N-TypeCentral Nervous SystemHumansMaleCACNA1A protein, humanCACNA1F protein, humanCalciumCalcium ChannelsCalcium Channels, L-TypeCalcium Channels, N-TypeCACNA1ACACNA1Fcalcium channelchannelopathyhemiplegic migraineimmune dysfunctionsporadic hemiplegic migraine type 1 (SHM1)

Identifiers

PMID36833327
PMCPMC9956337
OpenAlexW4319080766

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.