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[Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl)].

作者信息

Kölmel H W, Assmus H, Seiler D

出版信息

Arch Psychiatr Nervenkr (1970). 1974;218(2):93-106. doi: 10.1007/BF00343162.

DOI:10.1007/BF00343162
PMID:4522354
Abstract
摘要

相似文献

1
[Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl)].酸性麦芽糖酶缺乏所致肌病。青少年及成人庞贝病（作者译）
Arch Psychiatr Nervenkr (1970). 1974;218(2):93-106. doi: 10.1007/BF00343162.
2
[Glycogen storage disease (Pompe's disease) presenting as myopathy in the adult (author's transl)].成人期表现为肌病的糖原贮积病（庞贝病）（作者译）
Dtsch Med Wochenschr. 1977 Oct 21;102(42):1512-4. doi: 10.1055/s-0028-1105529.
3
Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies.成人酸性麦芽糖酶缺乏症：对四例可能酷似肌营养不良或其他肌病的综合征病例的研究。
Brain. 1970;93(3):599-616. doi: 10.1093/brain/93.3.599.
4
Fine structure of skeletal muscle in type-3 glycogenosis.Ⅲ型糖原贮积病中骨骼肌的精细结构
Arch Pathol. 1969 Aug;88(2):130-6.
5
Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle.
Acta Neuropathol. 1973 Feb 19;23(3):229-44. doi: 10.1007/BF00687878.
6
[Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies].[成人型酸性麦芽糖酶缺乏症（庞贝病）的缓解形式。形态学和病理生物化学研究]
Klin Wochenschr. 1983 Aug 1;61(15):743-50. doi: 10.1007/BF01497401.
7
[Results of clinical, biochemical, light-microscopical and ultrastructural studies of childhood glycogenosis in two brothers and their sister (author's transl)].
Z Kinderheilkd. 1973 Dec 12;116(1):23-41.
8
Adult myopathy from glycogen storage disease due to acid maltase deficiency.由于酸性麦芽糖酶缺乏导致糖原贮积病引起的成人肌病。
Brain. 1968 Sep;91(3):435-62. doi: 10.1093/brain/91.3.435.
9
[Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)].成人假肥大性肌肉糖原贮积症（酸性麦芽糖酶缺乏综合征）（作者译）
J Neurol. 1976;213(3):199-216. doi: 10.1007/BF00312870.
10
[Acid maltase deficiency myopathy infantile and adult forms (author's transl)].酸性麦芽糖酶缺乏性肌病（婴儿型和成人型）（作者译）
Arch Neurobiol (Madr). 1981 Jan-Feb;44(1):49-62.

引用本文的文献

1
The natural course of non-classic Pompe's disease; a review of 225 published cases.非典型庞贝氏病的自然病程；对225例已发表病例的综述
J Neurol. 2005 Aug;252(8):875-84. doi: 10.1007/s00415-005-0922-9.
2
[High frequency discharges as a non-specific EMG activity in adult acid maltase deficiency (author's transl)].[高频放电作为成人酸性麦芽糖酶缺乏症中的一种非特异性肌电图活动（作者译）]
Arch Psychiatr Nervenkr (1970). 1980;228(1):45-51. doi: 10.1007/BF00365743.
3
[Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies].

本文引用的文献

1
A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASE.一种在成人期出现、具有提示糖原贮积病特征的肌病。
J Neurol Neurosurg Psychiatry. 1960 Nov;23(4):302-11. doi: 10.1136/jnnp.23.4.302.
2
VACUOLAR MYOPATHY: CLINICAL, HISTOCHEMICAL, AND MICROSCOPIC STUDY.空泡性肌病：临床、组织化学及显微镜研究
Arch Neurol. 1965 Jun;12:570-82. doi: 10.1001/archneur.1965.00460300018003.
3
CONGENITAL NONPROGRESSIVE MYOPATHY. CENTRAL CORE DISEASE AND NEMALINE MYOPATHY IN ONE FAMILY.先天性非进行性肌病。一个家族中的中央轴空病和杆状体肌病
[成人型酸性麦芽糖酶缺乏症（庞贝病）的缓解形式。形态学和病理生物化学研究]
Klin Wochenschr. 1983 Aug 1;61(15):743-50. doi: 10.1007/BF01497401.
4
[Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)].成人假肥大性肌肉糖原贮积症（酸性麦芽糖酶缺乏综合征）（作者译）
J Neurol. 1976;213(3):199-216. doi: 10.1007/BF00312870.
5
Acid maltase deficiency in non-identical adult twins. A morphological and biochemical study.非同卵成年双胞胎中的酸性麦芽糖酶缺乏症。一项形态学和生物化学研究。
J Neurol. 1976 Aug 6;213(2):105-18. doi: 10.1007/BF00313272.
6
The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult.成人II型糖原贮积病（庞贝病）的症状学、形态学及生物化学
J Neurol. 1976 Jun 14;212(3):237-52. doi: 10.1007/BF00314526.
Neurology. 1965 Apr;15:371-81. doi: 10.1212/wnl.15.4.371.
4
Skeletal muscle glycogenosis: an investigation of two dissimilar cases.骨骼肌糖原贮积症：两例不同病例的调查
J Neurol Neurosurg Psychiatry. 1963 Feb;26(1):60-8. doi: 10.1136/jnnp.26.1.60.
5
alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).全身性糖原贮积病（庞贝氏病）中的α-葡萄糖苷酶缺乏症。
Biochem J. 1963 Jan;86(1):11-6. doi: 10.1042/bj0860011.
6
Amylo-1, 6-glucosidase in muscle tissue in generalized glycogen storage disease.全身性糖原贮积病中肌肉组织的淀粉-1,6-葡萄糖苷酶
J Biol Chem. 1956 Jan;218(1):123-9.
7
Pre-clinical muscular dystrophy: histopathological changes observed on muscle biopsy.临床前肌营养不良：肌肉活检观察到的组织病理学变化。
Brain. 1967 Sep;90(3):565-76. doi: 10.1093/brain/90.3.565.
8
Correlation between electromyographic findings and muscle biopsy in ccases of neuromuscular diseease.神经肌肉疾病病例中肌电图检查结果与肌肉活检的相关性。
J Neurol Sci. 1971 May;13(1):85-106. doi: 10.1016/0022-510x(71)90209-7.
9
Acid maltase levels in muscle in heterozygous acid maltase deficiency and in non-weak and neuromuscular disease controls.杂合性酸性麦芽糖酶缺乏症患者肌肉中的酸性麦芽糖酶水平以及非虚弱型和神经肌肉疾病对照者肌肉中的酸性麦芽糖酶水平。
J Neurol Neurosurg Psychiatry. 1970 Dec;33(6):801-4. doi: 10.1136/jnnp.33.6.801.
10
Adult myopathy from glycogen storage disease due to acid maltase deficiency.由于酸性麦芽糖酶缺乏导致糖原贮积病引起的成人肌病。
Brain. 1968 Sep;91(3):435-62. doi: 10.1093/brain/91.3.435.