TREAT-NMD研讨会：利用肌肉磁共振成像进行遗传性肌肉疾病的模式识别：2011年2月25日至26日，意大利罗马 - Suppr

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超能文献

TREAT-NMD workshop: pattern recognition in genetic muscle diseases using muscle MRI: 25-26 February 2011, Rome, Italy.

作者信息

Straub Volker, Carlier Pierre G, Mercuri Eugenio

机构信息

Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S42-53. doi: 10.1016/j.nmd.2012.08.002.

DOI:10.1016/j.nmd.2012.08.002

PMID:22980768

Abstract

摘要

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TREAT-NMD workshop: pattern recognition in genetic muscle diseases using muscle MRI: 25-26 February 2011, Rome, Italy.

作者信息

Straub Volker, Carlier Pierre G, Mercuri Eugenio

机构信息

Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S42-53. doi: 10.1016/j.nmd.2012.08.002.

DOI:10.1016/j.nmd.2012.08.002

PMID:22980768

Abstract

摘要

相似文献

TREAT-NMD workshop: pattern recognition in genetic muscle diseases using muscle MRI: 25-26 February 2011, Rome, Italy.

Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S42-53. doi: 10.1016/j.nmd.2012.08.002.

Whole body muscle MRI protocol: pattern recognition in early onset NM disorders.

Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S68-84. doi: 10.1016/j.nmd.2012.08.003.

Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S54-67. doi: 10.1016/j.nmd.2012.06.005.

Whole-body muscle magnetic resonance imaging in SEPN1-related myopathy shows a homogeneous and recognizable pattern.

Muscle Nerve. 2015 Nov;52(5):728-35. doi: 10.1002/mus.24634. Epub 2015 Sep 14.

Symptomatic dysferlin gene mutation carriers: characterization of two cases.

Neurology. 2007 Apr 17;68(16):1284-9. doi: 10.1212/01.wnl.0000256768.79353.60. Epub 2007 Feb 7.

Locomotor system assessment by muscle magnetic resonance imaging.

Magn Reson Q. 1991 Apr;7(2):79-103.

[Magnetic resonance tomography in generalized skeletal muscle diseases. Examination modalities and indications recommendations].

Rontgenpraxis. 1989 Oct;42(10):338-45.

Magnetic resonance imaging of skeletal muscle.

Curr Opin Neurol. 2007 Oct;20(5):595-9. doi: 10.1097/WCO.0b013e3282efc322.

Applications of MRI in muscle diseases.

Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S41. doi: 10.1016/j.nmd.2012.08.001.

Magnetic resonance imaging of muscle disease: a pattern-based approach.

Muscle Nerve. 2012 Oct;46(4):465-81. doi: 10.1002/mus.23370.

引用本文的文献

Multi-parametric quantitative MRI of the lower limb muscles in a longitudinal study of limb-girdle muscular dystrophy R9.

PLoS One. 2025 Apr 28;20(4):e0321463. doi: 10.1371/journal.pone.0321463. eCollection 2025.

[Expert recommendations for magnetic resonance imaging of muscle disorders].

Nervenarzt. 2024 Aug;95(8):721-729. doi: 10.1007/s00115-024-01673-x.

[Expert recommendations for magnetic resonance imaging of muscle disorders].

Radiologie (Heidelb). 2024 Aug;64(8):653-662. doi: 10.1007/s00117-024-01276-2. Epub 2024 Apr 19.

Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophy.

J Neurol. 2023 Dec;270(12):5988-5998. doi: 10.1007/s00415-023-11906-9. Epub 2023 Aug 27.

Misdiagnosis of polymyositis in a young female patient with occult limb-girdle muscular dystrophy.

Rheumatol Adv Pract. 2023 Jul 11;7(2):rkad061. doi: 10.1093/rap/rkad061. eCollection 2023.

Utility of Skeletal Muscle CT in Diagnosing Spinal Muscular Atrophy Type 3 in a Patient Who Had Been Undiagnosed for 50 Years.

Cureus. 2023 May 8;15(5):e38709. doi: 10.7759/cureus.38709. eCollection 2023 May.

A Case of Cardiogenic Stroke With a Novel LMNA Variant (c. 1135C>A; p.Leu379Ile).

Cureus. 2023 Apr 19;15(4):e37824. doi: 10.7759/cureus.37824. eCollection 2023 Apr.

Unraveling the Molecular Basis of the Dystrophic Process in Limb-Girdle Muscular Dystrophy LGMD-R12 by Differential Gene Expression Profiles in Diseased and Healthy Muscles.

Cells. 2022 Apr 30;11(9):1508. doi: 10.3390/cells11091508.

Diagnostics (Basel). 2021 Jun 8;11(6):1056. doi: 10.3390/diagnostics11061056.

Functional Ambulation Profile (FAP) Score as a Potential Marker of Gait Analysis in Myotonic Dystrophy Type 1.

Front Neurol. 2020 May 19;11:392. doi: 10.3389/fneur.2020.00392. eCollection 2020.