Evidence map›Paper›PMID 33897931›Full record

ArticleRadiology case reports2021

Silent Moyamoya disease - A rare case report.

Juna Musa, Masum Rahman, Ali Guy, Angela Guy, Kristi Saliaj, Abu Bakar Siddik, Fjolla Hyseni, Ketjana Elezi, Ina Kola, Anisa Cobo and 1 more

Erratum issuedOpen access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Radiology case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 2 countries.

Juna MusaDepartment of Surgery Physiology and Biomedical Engineering, Mayo Clinic, 200 1st St, SW Floor 8 Rochester, MN, 55905, USA.
Masum RahmanDepartment of Neurological Surgery, Mayo Clinic, 200 1st St, SW Floor 8, Rochester, MN, 55905, USA.
Ali GuyDepartment of Physical Medicine and Rehabilitation, New York University, School of Medicine, NYU Medical Center, 550 1st Avenue, New York, NY, 10016, USA.
Angela GuyHealth Emphasis California School of Professional Psychology Alliant International University, 1000 South Fremont Ave, Unit 5, Alhambra, CA, 91803, USA.
Kristi SaliajMother Teresa hospital university, Rruga e Dibrës 372, Tirana, AL, 1000, Albania.
Abu Bakar SiddikDepartment of Pain Medicine, Mayo Clinic, 4500 San Pablo Rd S, Jacksonville, FL, 32224, USA.
Fjolla HyseniDepartment of Urology, NYU Langone Health, 11th and 12th Floors, 222 E 41st St, New York, NY, 10017, USA.
Ketjana EleziPharmacist and master in Health management, University of Medicine, Tirana, AL, 1000, Albania.
Ina KolaDepartment of Burns and Plastic Surgery, Mother Teresa Hospital, Rruga e Dibrës 372, Tirana, AL, 1000 Albania.
Anisa CoboUniversity of Medicine, Tirana, AL, 1000, Albania.
Ilir AhmetgjekajUniversity Clinical Center, Clinic of Radiology, University For Business and Technology -Radiology, Pristina, Kosovo.
Mother Teresa Hospital · ALNew York University · USUniversity of Medicine Tirana · ALMayo Clinic · USMayo Clinic in Florida · USNYU Langone Health · USWinnMed · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Moyamoya is a rare cerebrovascular disorder marked by chronic, gradual blockage of the circle of Willis arteries, leading to characteristic collateral vessels, specifically cerebral angiography. The disease can develop in children and adults, although there are different clinical characteristics. Moyamoya disease occurs mainly in Japanese people but has been reported in all races of varying age distributions and clinical features. As a reason, Moyamoya disease has been under-recognized as a cause of hemorrhagic and ischemic strokes in Western nations. There is no proven solution at this time, and there is debate over current care methods. The authors identify a case of a 40-year-old male with a small subcutaneous nevus-like mass in his left orbit who was diagnosed with Moyamoya disease.

Indexed as

AngiographyCerebralCerebrovascular arteriopathyIschemic strokeMoyamoya syndromeRadiological findings

Identifiers

PMID33897931
PMCPMC8055531
OpenAlexW3154174602

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.