Quantitative vs qualitative muscle MRI: Imaging biomarker in patients with Oculopharyngeal Muscular Dystrophy (OPMD)
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference38 articles.
1. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat Genet,1998
2. A study of impairments in oculopharyngeal muscular dystrophy;Brisson;Muscle Nerve,2020
3. Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene;Blumen;Neurology,2000
4. [Haplotype Analysis of Oculopharyngeal Muscular Dystrophy (OPMD) Locus in Yakutia];Marusin;Genetika,2016
5. Oculopharyngeal muscular dystrophy in Hispanic New Mexicans;Becher;JAMA,2001
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1. Muscle MRI in Patients With Oculopharyngeal Muscular Dystrophy;Neurology;2024-01-09
2. Muscle diffusion MRI reveals autophagic buildup in a mouse model for Pompe disease;Scientific Reports;2023-12-20
3. Emerging and established biomarkers of oculopharyngeal muscular dystrophy;Neuromuscular Disorders;2023-11
4. Muscle Imaging in Muscular Dystrophies;Current Clinical Neurology;2023
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