伴有面肩肱分布的炎性肌病。 - Suppr

Inflammatory myopathy with facioscapulohumeral distribution.

作者信息

Munsat T L, Piper D, Cancilla P, Mednick J

出版信息

Neurology. 1972 Apr;22(4):335-47. doi: 10.1212/wnl.22.4.335.

DOI:10.1212/wnl.22.4.335

PMID:5062826

Abstract

摘要

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Inflammatory myopathy with facioscapulohumeral distribution.

Neurology. 1972 Apr;22(4):335-47. doi: 10.1212/wnl.22.4.335.

The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndrome.

J Neurol Sci. 1973 Mar;18(3):351-8. doi: 10.1016/0022-510x(73)90083-x.

[Effect of drug administration on the child with progressive muscular dystrophy].

Iryo. 1969 Oct;23(10):1319-27.

[Changes in the activity of blood serum enzymes in relatives of children with myopathy].

Vopr Med Khim. 1966 Nov-Dec;12(6):600-3.

Carrier detection in X-linked Duchenne type muscular dystrophy. A pluridimensional investigation.

J Neurol Sci. 1968 Mar-Apr;6(2):289-300. doi: 10.1016/0022-510x(68)90097-x.

Blood enzymes in Duchene's progressive muscular dystrophy and their correlation with the clinical and histological pictures.

Acta Med Pol. 1970;11(4):387-93.

[Enzymatic activity of the serum in the family of a progressive muscular dystrophy patient].

Iryo. 1969 Oct;23(10):1306-11.

[X-linked myotubular myopathy].

Zh Nevropatol Psikhiatr Im S S Korsakova. 1979;79(10):1334-8.

Serum enzyme alterations in neuromuscular disorders.

JAMA. 1973 Dec 24;226(13):1536-43.

Benign sex-linked muscular dystrophy. Clinical and pathological features.

Neurology. 1969 Jul;19(7):617-33. doi: 10.1212/wnl.19.7.617.

引用本文的文献

Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy.

Hum Mol Genet. 2024 May 4;33(10):872-883. doi: 10.1093/hmg/ddae019.

Pathomechanisms and biomarkers in facioscapulohumeral muscular dystrophy: roles of DUX4 and PAX7.

EMBO Mol Med. 2021 Aug 9;13(8):e13695. doi: 10.15252/emmm.202013695. Epub 2021 Jun 21.

Profiling Serum Antibodies Against Muscle Antigens in Facioscapulohumeral Muscular Dystrophy Finds No Disease-Specific Autoantibodies.

J Neuromuscul Dis. 2021;8(5):801-814. doi: 10.3233/JND-210653.

Therapeutic Approaches in Facioscapulohumeral Muscular Dystrophy.

Trends Mol Med. 2021 Feb;27(2):123-137. doi: 10.1016/j.molmed.2020.09.008. Epub 2020 Oct 19.

DUX4 expressing immortalized FSHD lymphoblastoid cells express genes elevated in FSHD muscle biopsies, correlating with the early stages of inflammation.

Hum Mol Genet. 2020 Aug 11;29(14):2285-2299. doi: 10.1093/hmg/ddaa053.

Immunobiology of Inherited Muscular Dystrophies.

Compr Physiol. 2018 Sep 14;8(4):1313-1356. doi: 10.1002/cphy.c170052.

Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy.

Mol Neurobiol. 2018 Apr;55(4):2959-2966. doi: 10.1007/s12035-017-0563-x. Epub 2017 Apr 29.

Facioscapulohumeral Dystrophy.

Curr Neurol Neurosci Rep. 2016 Jul;16(7):66. doi: 10.1007/s11910-016-0667-0.

Influence of immune responses in gene/stem cell therapies for muscular dystrophies.

Biomed Res Int. 2014;2014:818107. doi: 10.1155/2014/818107. Epub 2014 May 19.

Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).

PLoS Genet. 2013;9(1):e1003186. doi: 10.1371/journal.pgen.1003186. Epub 2013 Jan 3.

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Inflammatory myopathy with facioscapulohumeral distribution.

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