Evidence map›Paper›PMID 39126013›Full record

ArticleInternational journal of molecular sciences2024

Case Report: A Case of a Patient with Smith-Magenis Syndrome and Early-Onset Parkinson's Disease.

Tchelet Stern, Yara Hussein, Diogo Cordeiro, Hagit Sadis, Tali Garin-Shkolnik, Ronen Spiegel, Sagit Cohen, Ruth Harari, Ilana Schlesinger, Shani Stern

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. 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

10 authors.

Tchelet SternSagol Department of Neurobiology, University of Haifa, Haifa 3103301, Israel.
Yara HusseinSagol Department of Neurobiology, University of Haifa, Haifa 3103301, Israel.ORCID 0000-0001-6173-8584
Diogo CordeiroSagol Department of Neurobiology, University of Haifa, Haifa 3103301, Israel.ORCID 0000-0003-2688-5233
Hagit SadisSagol Department of Neurobiology, University of Haifa, Haifa 3103301, Israel.ORCID 0009-0000-0723-0229
Tali Garin-ShkolnikCenter for Rare Diseases, Emek Medical Center, Afula 1834111, Israel.
Ronen SpiegelPediatric Department B, Emek Medical Center, Afula 1834111, Israel.
Sagit CohenNofim, Daycare, Migdal 1495000, Israel.
Ruth HarariNofim, Daycare, Migdal 1495000, Israel.
Ilana SchlesingerDepartment of Neurology, Rambam Health Care Campus, Haifa 3109601, Israel.
Shani SternSagol Department of Neurobiology, University of Haifa, Haifa 3103301, Israel.ORCID 0000-0002-2644-7068

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Smith-Magenis Syndrome (SMS) is a rare genetic disorder, characterized by intellectual disability (ID), behavioral impairments, and sleep disturbances, as well as multiple organ anomalies in some affected individuals. The syndrome is caused by a deletion in the chromosome band around 17p11.2, including the Retinoic Acid Induced 1 (

Indexed as

Parkinson DiseaseSmith-Magenis SyndromeAge of OnsetDNA Copy Number VariationsFemaleHumansMaleMiddle AgedTrans-ActivatorsRAI1 protein, humanTrans-ActivatorsIDneurodegenerative diseasePDRAI1SMS

Identifiers

PMID39126013
PMCPMC11313365

What Socratic 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 Socratic graph.