ArticleClinical case reports2022
Moyamoya syndrome in a child with HbEβ-thalassemia.
Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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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.
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Who cites it
4 citing papers in PubMed, 7 citations in OpenAlex.
- Orofacial features and dental management of a pediatric patient with moyamoya disease-A one year follow up.Clinical case reports · 2024Article
- Beta-Thalassemia Presenting as Moyamoya Syndrome With a Review of Skeletal Manifestations.Cureus · 2023Article
- Moyamoya syndrome with ruptured aneurysm in α-thalassemia: A case report.Experimental and therapeutic medicine · 2022Article
- Moyamoya syndrome in a child with HbEβ-thalassemia.Clinical case reports · 2022Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Moyamoya is a progressive cerebrovascular disease associated with stenosis or occlusion of the arteries of the Circle of Willis. It is uncommon in thalassemia. We present a 9-year-old girl with HbEβ-thalassemia who presented with headache, vomiting, and episodes of transient hemiparesis with complete occlusion internal carotid arteries.
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Registered trials
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.