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Multicore disease: report of a case with onset in middle age.

作者信息

Bonnette H, Roelofs R, Olson W H

出版信息

Neurology. 1974 Nov;24(11):1039-44. doi: 10.1212/wnl.24.11.1039.

DOI:10.1212/wnl.24.11.1039
PMID:4153807
Abstract
摘要

相似文献

1
Multicore disease: report of a case with onset in middle age.多核病:一例中年起病病例报告
Neurology. 1974 Nov;24(11):1039-44. doi: 10.1212/wnl.24.11.1039.
2
The fine structural differences in human muscle fiber types based on peroxidatic activity.基于过氧化物酶活性的人类肌纤维类型的精细结构差异。
J Neuropathol Exp Neurol. 1974 Oct;33(5):632-40. doi: 10.1097/00005072-197410000-00005.
3
Congenital rod disease. Further evidence of innervational abnormalities as the basis for the clinicopathologic features.先天性视杆细胞疾病。神经支配异常作为临床病理特征基础的进一步证据。
J Neurol Sci. 1974 Nov;23(3):371-85. doi: 10.1016/0022-510x(74)90155-5.
4
Chronic benign congenital myopathy: fingerprint body type.慢性良性先天性肌病:指纹体型。
Can J Neurol Sci. 1974 May;1(2):106-13. doi: 10.1017/s031716710001965x.
5
The effect of immobilization and exercise on acetylcholine-mediated myopathies.固定和运动对乙酰胆碱介导的肌病的影响。
Neurology. 1974 Nov;24(11):1086-90. doi: 10.1212/wnl.24.11.1086.
6
[Comparison of muscular histoenzymological and electromyographic findings in human neuromuscular pathology. Methods and preliminary results].[人类神经肌肉病理学中肌肉组织酶学和肌电图检查结果的比较。方法与初步结果]
Rev Neurol (Paris). 1974 Jan-Feb;130(1-2):5-19.
7
Zebra body myopathy. Clinical, histochemical and ultrastructural studies.
J Neurol Sci. 1975 Apr;24(4):437-46. doi: 10.1016/0022-510x(75)90169-0.
8
Hypotrophic type I muscle fibres with central nuclei, and central myofibrillar lysis preferentially involving type II fibres.具有中央核的I型萎缩肌纤维,以及优先累及II型纤维的中央肌原纤维溶解。
Eur Neurol. 1974;11(2):108-27. doi: 10.1159/000114311.
9
Central core disease. A study of clinically unaffected muscle.中央轴空病。对临床未受累肌肉的一项研究。
J Neurol Sci. 1973 Jun;19(2):207-23. doi: 10.1016/0022-510x(73)90163-9.
10
Diagnostic accuracy of clinical data, quantitative electromyography and histochemistry in neuromuscular disease. A study of 105 cases.临床数据、定量肌电图和组织化学在神经肌肉疾病中的诊断准确性。一项对105例病例的研究。
J Neurol Sci. 1974 Jan;21(1):59-70. doi: 10.1016/0022-510x(74)90106-3.

引用本文的文献

1
Multi-minicore Disease.多微核疾病
Orphanet J Rare Dis. 2007 Jul 13;2:31. doi: 10.1186/1750-1172-2-31.
2
Multicore myopathy associated with multiple pterygium syndrome and hypertrophic cardiomyopathy.
Pediatr Cardiol. 1996 Jan-Feb;17(1):53-6. doi: 10.1007/BF02505814.
3
Minicore myopathy.
Klin Wochenschr. 1982 Nov 2;60(21):1351-5. doi: 10.1007/BF01716214.
4
Autosomal dominant multicore disease.
常染色体显性多核疾病。
J Neurol Neurosurg Psychiatry. 1982 Apr;45(4):360-5. doi: 10.1136/jnnp.45.4.360.
5
Adult-onset mixed myopathy with nemaline rods, minicores, and central cores: a muscle disorder mimicking polymyositis.成人起病的伴有杆状体、微小核心和中央核心的混合性肌病:一种酷似多发性肌炎的肌肉疾病。
J Neurol. 1984;231(3):103-8. doi: 10.1007/BF00313674.
6
Pleocore disease. Multi-minicore disease and focal loss of cross striations.
Acta Neuropathol. 1986;72(2):142-9. doi: 10.1007/BF00685976.
7
Multicore disease in twins.
J Neurol Neurosurg Psychiatry. 1976 Jun;39(6):602-6. doi: 10.1136/jnnp.39.6.602.
8
Focal abnormalities in mitochondrial distribution in muscle. Two atypical cases of so-called "central core disease".
Acta Neuropathol. 1977 Jul 15;39(1):25-31. doi: 10.1007/BF00690382.
9
Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter.中央轴空病:父女肌肉活检组织化学及超微结构研究
J Neurol. 1978 Apr 14;218(1):55-62. doi: 10.1007/BF00314719.
10
Electromyographic findings in the so-called non-progressive myopathies.
J Neurol. 1976 Feb 13;211(3):241-51. doi: 10.1007/BF00313234.