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[On the storage of mucopolysaccharide-like substances in the brain in generalized glycogenosis (type II)].

作者信息

Schnabel R

出版信息

Acta Neuropathol. 1965 Jul 1;4(6):646-58. doi: 10.1007/BF00691215.

DOI:10.1007/BF00691215
PMID:4223251
Abstract
摘要

相似文献

1
[On the storage of mucopolysaccharide-like substances in the brain in generalized glycogenosis (type II)].[关于全身性糖原贮积病（II型）中脑内类粘多糖物质的储存]
Acta Neuropathol. 1965 Jul 1;4(6):646-58. doi: 10.1007/BF00691215.
2
NEUROPATHOLOGICAL AND NEUROCHEMICAL ASPECTS OF GENERALIZED GLYCOGEN STORAGE DISEASE.全身性糖原贮积病的神经病理学和神经化学方面
J Neurol Neurosurg Psychiatry. 1963 Oct;26(5):422-30. doi: 10.1136/jnnp.26.5.422.
3
Nonglycogen polysaccharide storage in glycogenosis type 2 (Pompe's disease).2型糖原贮积病（庞贝氏病）中的非糖原多糖储存
Arch Pathol. 1968 Dec;86(6):579-84.
4
[PROGRESSIVE MYOCLONIC EPILEPSY AS A THESAURISMOSIS].[进行性肌阵挛癫痫作为一种贮积症]
Rev Neurol (Paris). 1963 Jun;108:932-5.
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GENERALIZED GLYCOGENOSIS. REPORT OF A CASE WITH DEFICIENCY OF ALPHA GLUCOSIDASE.
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[Clinical, biochemical, morphological and electrophysiological studies of glycogenosis Type II in childhood with double deficiency of enzymes (author's transl)].儿童期Ⅱ型糖原贮积病伴酶双缺乏的临床、生化、形态学及电生理研究（作者译）
Z Kinderheilkd. 1975 Jul 1;120(1):19-28.
7
Administration of a mixture of fungal glucosidases to a patient with type II glycogenosis (Pompe's disease).向一名患有II型糖原贮积病（庞贝氏病）的患者施用真菌糖苷酶混合物。
Pediatrics. 1968 Oct;42(4):672-6.
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GLYCOGEN STORAGE DISEASE. BIOCHEMICAL AND CLINICAL DATA IN SIXTEEN CASES.糖原贮积病。16例的生化及临床资料
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Glycogenosis type II: glycogen storage in cell cultures from muscle.II型糖原贮积病：肌肉细胞培养物中的糖原蓄积
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FUTURE TRENDS IN THE INVESTIGATION OF GLYCOGEN STORAGE DISEASE.糖原贮积病研究的未来趋势
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[Central nervous system deposits in protractive (Lundborg-type myoclonic bodies disease].[迁延性（伦德伯格型肌阵挛体病中的中枢神经系统沉积物]
Acta Neuropathol. 1969;12(3):260-75. doi: 10.1007/BF00687649.
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[Histochemistry of mucopolysaccharide-like substances (basophilic substances) in skeletal muscle in neuromuscular glycogenosis (type II)].

本文引用的文献

1
Glycogen disease resembling mongolism, cretinism, and amytonia congenita; case report and review of literature.
J Pediatr. 1950 Jan;36(1):11-30, illust. doi: 10.1016/s0022-3476(50)80174-9.
2
[Basophil (mucoid) degeneration of the myocardium].[心肌嗜碱性（黏液样）变性]
Z Kreislaufforsch. 1952 Jan;41(1-2):42-9.
3
[On the question of the specificity of the saliva test in the histochemical determination of glycogen].[关于唾液检测在糖原组织化学测定中的特异性问题]
Acta Anat (Basel). 1961;47:66-73.
[神经肌肉性糖原贮积病（II型）中骨骼肌黏多糖样物质（嗜碱性物质）的组织化学]
Acta Neuropathol. 1971;17(2):169-78. doi: 10.1007/BF00687492.
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.
4
[On the histological demonstration of the viscosity carrier (carboxymethylcellulose) in water-soluble contrast medium].[关于水溶性造影剂中粘度载体（羧甲基纤维素）的组织学显示]
Acta Histochem. 1959 Oct 13;8:50-9.
5
[Leukodystrophy, Scholz' type, (metachromatic form of diffuse sclerosis) with sphinolipoidosis (cerebroside-sulfuric acid ester storage disease)].[舒尔茨型脑白质营养不良（弥漫性硬化的异染性形式）伴鞘脂沉积症（脑苷脂 - 硫酸酯贮积病）]
Hoppe Seylers Z Physiol Chem. 1960 May 31;318:265-77. doi: 10.1515/bchm2.1960.318.1.265.
6
Glycogen disease of skeletal muscle; report of two cases and review of literature.骨骼肌糖原贮积病；两例报告及文献复习
Pediatrics. 1955 Jun;15(6):715-32.
7
POMPE'S DISEASE (DIFFUSE GLYCOGENOSIS) WITH NEURONAL STORAGE.庞贝氏病（弥漫性糖原贮积症）伴神经元贮积
J Neuropathol Exp Neurol. 1965 Jan;24:85-96. doi: 10.1097/00005072-196501000-00008.
8
[A NEW STAINING TECHNIC FOR GLIA FIBERS].[一种用于神经胶质纤维的新染色技术]
Mikroskopie. 1963 Aug;18:92-5.
9
[THE MYOCLONUS BODY DISEASE. A CONGENITAL DISORDER OF THE CARBOHYDRATE METABOLISM. CLINICOPATHOLOGICAL STUDY OF 5 CASES].[肌阵挛身体疾病。一种碳水化合物代谢的先天性疾病。5例临床病理研究]
Fortschr Neurol Psychiatr Grenzgeb. 1964 Jul;32:305-45.
10
GLYCOGENOSIS TYPE 1 (LACK OF GLUCOSE-6-PHOSPHATASE) IN FOUR SIBLINGS.四名兄弟姐妹患1型糖原贮积病（缺乏葡萄糖-6-磷酸酶）。
Acta Paediatr (Stockh). 1964;58:SUPPL 157:1-28.