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Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case.

作者信息

Canal N, Frattola L, Pellegrini G

出版信息

Z Neurol. 1972;201(2):98-108. doi: 10.1007/BF00316197.

DOI:10.1007/BF00316197
PMID:4112649
Abstract
摘要

相似文献

1
Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case.II型骨骼肌糖原贮积症:1例的生化及电子显微镜研究
Z Neurol. 1972;201(2):98-108. doi: 10.1007/BF00316197.
2
Glycogen metabolism of human diploid fibroblast cells in culture. I. Studies of cells from patients with glycogenosis types II, 3, and V.培养的人二倍体成纤维细胞的糖原代谢。I. 对II型、3型和V型糖原贮积症患者细胞的研究。
Pediatr Res. 1973 Sep;7(9):739-44. doi: 10.1203/00006450-197309000-00002.
3
Lysosomal glycogen storage disease with normal acid maltase.酸性麦芽糖酶正常的溶酶体糖原贮积病
Neurology. 1981 Jan;31(1):51-7. doi: 10.1212/wnl.31.1.51.
4
Type 3 glycogenosis. A biochemical and electron microscopic study.III型糖原贮积病。一项生化与电子显微镜研究。
Lab Invest. 1970 May;22(5):468-77.
5
[Muscular glycogenosis. A biochemical study].
Ann Anat Pathol (Paris). 1973 Apr-Jun;18(2):169-94.
6
[A vacuolar myopathy: autophagic glycogenosis of late onset. Ultrastructural study].[一种空泡性肌病:迟发性自噬性糖原贮积症。超微结构研究]
Ann Anat Pathol (Paris). 1971 Jan-Mar;16(1):47-54.
7
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.
8
[Histochemical and ultrastructural study of a case of type 3 glycogenosis].[一例3型糖原贮积病的组织化学和超微结构研究]
Ann Anat Pathol (Paris). 1971 Jan-Mar;16(1):85-92.
9
[Electron microscopic study of liver and muscles in two cases of type 3 glycogenosis].[3型糖原贮积症两例肝脏和肌肉的电子显微镜研究]
Pathol Eur. 1972;7(2):112-25.
10
Control of glycogen metabolism in human muscle. Evidence from glycogen storage diseases.人类肌肉中糖原代谢的调控。来自糖原贮积病的证据。
Arch Neurol. 1970 Dec;23(6):534-40. doi: 10.1001/archneur.1970.00480300056007.

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
The glycogen storage diseases.糖原贮积病
J Clin Pathol Suppl (R Coll Pathol). 1974;8:106-21.
3
[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)

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
Phosphorylase and glycogen levels in skeletal muscle and liver of hibernating and non-hibernating bats.冬眠和非冬眠蝙蝠骨骼肌与肝脏中的磷酸化酶及糖原水平
Am J Physiol. 1959 Nov;197:1059-62. doi: 10.1152/ajplegacy.1959.197.5.1059.
3
Glycogen disease of skeletal muscle; report of two cases and review of literature.
Arch Psychiatr Nervenkr (1970). 1974;218(2):93-106. doi: 10.1007/BF00343162.
4
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.
5
[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.
6
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.
7
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.
骨骼肌糖原贮积病;两例报告及文献复习
Pediatrics. 1955 Jun;15(6):715-32.
4
PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.骨骼肌磷酸果糖激酶缺乏症。一种新型糖原累积病。
Biochem Biophys Res Commun. 1965 May 3;19:517-23. doi: 10.1016/0006-291x(65)90156-7.
5
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.
6
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.
7
Glycogen storage disease of the muscles. Report of a case with unusual features.肌肉糖原贮积病。1例具有不寻常特征的病例报告。
J Pediatr. 1962 Sep;61:438-42. doi: 10.1016/s0022-3476(62)80375-8.
8
Determination glycogen.糖原的测定
Arch Biochem Biophys. 1957 Apr;67(2):378-86. doi: 10.1016/0003-9861(57)90292-8.
9
A new myopathy due to glycolytic abnormalities.一种由糖酵解异常引起的新型肌病。
Trans Am Neurol Assoc. 1965;90:46-8.
10
Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease.II型糖原贮积病患儿组织中同时缺乏α-1,4-葡萄糖苷酶和α-1,6-葡萄糖苷酶活性(pH 4)
Biochemistry. 1970 Mar 17;9(6):1423-8. doi: 10.1021/bi00808a017.