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The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome.

作者信息

Ricker K, Mertens H G

出版信息

Eur Neurol. 1968;1(5):275-307. doi: 10.1159/000113669.

DOI:10.1159/000113669
PMID:5696602
Abstract
摘要

相似文献

1
The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome.肌源性（面）肩胛-腓骨综合征的鉴别诊断。
Eur Neurol. 1968;1(5):275-307. doi: 10.1159/000113669.
2
Facio-scapulo-humeral muscular dystrophy in a patient with one paretic leg due to poliomyelitis.一名因小儿麻痹症导致单腿麻痹的患者患面肩肱型肌营养不良症。
J Neurol Sci. 1970 Jan;10(1):1-10. doi: 10.1016/0022-510x(70)90087-0.
3
[Diagnostic problems posed by hypotrophic facio-scapulo-humeral syndromes (author's transl)].[营养不良性面肩肱综合征引发的诊断问题（作者译）]
Ateneo Parmense Acta Biomed. 1976 Jan-Feb;47(1):95-101.
4
Muscular dystrophy in childhood.儿童期肌肉萎缩症
Dev Med Child Neurol. 1974 Feb;16(1):97-111. doi: 10.1111/j.1469-8749.1974.tb02723.x.
5
Nondystrophinopathic muscular dystrophies including myotonic dystrophy.非肌营养不良性肌营养不良症，包括强直性肌营养不良症。
Semin Pediatr Neurol. 1996 Jun;3(2):110-21. doi: 10.1016/s1071-9091(96)80040-4.
6
[Clinical aspects and therapy of muscular dystrophies].[肌肉萎缩症的临床症状与治疗]
Internist (Berl). 1972 Mar;13(3):108-17.
7
[Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood].
Klin Padiatr. 1986 Mar-Apr;198(2):119-21. doi: 10.1055/s-2008-1026865.
8
[Scapulo-peroneal myopathies 14 cases including 8 with facial involvement].肩胛腓骨肌病14例，其中8例累及面部
Sem Hop. 1969 Oct 26;45(43):2678-83.
9
[Progressive muscular dystrophy--limb-girdle and face-scapula-humerus types].[进行性肌营养不良——肢带型和面肩肱型]
Neurol Neurochir Psychiatr Pol. 1966 Nov;16(11):1257-64.
10
[Rapidly progressing facio-scapulo-humero-femoro-peroneal muscular dystrophy with sensorineural deafness].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1991;91(9):5-8.

引用本文的文献

1
Neurogenic scapuloperoneal syndrome in childhood.儿童神经源性肩胛腓骨综合征
J Neurol Neurosurg Psychiatry. 1980 Oct;43(10):888-96. doi: 10.1136/jnnp.43.10.888.
2
Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features.
J Neurol Neurosurg Psychiatry. 1981 Dec;44(12):1146-52. doi: 10.1136/jnnp.44.12.1146.
3
[New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias].
Humangenetik. 1972;16(3):181-200. doi: 10.1007/BF00273464.
4
The course of a model cutaneous inflammation in the scapuloperoneal syndrome and in systemic neuromuscular diseases.肩胛腓骨综合征及系统性神经肌肉疾病中典型皮肤炎症的病程。
J Neurol. 1974;208(2):139-46. doi: 10.1007/BF00312510.
5
X-linked scapuloperoneal syndrome.X连锁肩胛腓骨综合征
J Neurol Neurosurg Psychiatry. 1972 Apr;35(2):208-15. doi: 10.1136/jnnp.35.2.208.
6
Adult onset scapuloperoneal myopathy: diagnostic value of nerve morphometry and multiple muscle biopsies.成人起病的肩胛腓骨肌病：神经形态测量和多处肌肉活检的诊断价值
J Neurol Neurosurg Psychiatry. 1988 Jun;51(6):808-13. doi: 10.1136/jnnp.51.6.808.
7
Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophy.伴有神经源性面肩胛腓骨肌萎缩的家族性常染色体隐性遗传性僵硬脊柱综合征
J Neurol Neurosurg Psychiatry. 1991 Jan;54(1):42-5. doi: 10.1136/jnnp.54.1.42.
8
Scapuloperoneal atrophy with sensory involvement: Davidenkow's syndrome.伴有感觉受累的肩胛腓骨肌萎缩症：达维登科夫综合征。
J Neurol Neurosurg Psychiatry. 1975 Nov;38(11):1063-7. doi: 10.1136/jnnp.38.11.1063.
9
Adult onset scapuloperoneal myopathy.成人起病性肩胛腓骨肌病
J Neurol Neurosurg Psychiatry. 1975 Oct;38(10):1008-15. doi: 10.1136/jnnp.38.10.1008.
10
The differential diagnosis of scapuloperoneal amyotrophy.肩胛腓骨肌萎缩症的鉴别诊断
J Neurol. 1976 Jun 14;212(3):253-69. doi: 10.1007/BF00314527.