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SKELETAL MUSCLE GLYCOGENOSIS IN INDENTICAL TWINS.

作者信息

LEHOCZKY T, HALASY M, SIMON G, HARMOS G

出版信息

Br Med J. 1964 Sep 26;2(5412):802.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9a/1816520/3feb16b877e0/brmedj02569-0044-a.jpg

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本文引用的文献

1
McArdle's syndrome: phosphorylase-deficient myopathy.
Lancet. 1962 May 19;1(7238):1045-8. doi: 10.1016/s0140-6736(62)92145-1.
3
Glycogen storage disease of the muscles. Report of a case with unusual features.
J Pediatr. 1962 Sep;61:438-42. doi: 10.1016/s0022-3476(62)80375-8.
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Glycogen metabolism.
Physiol Rev. 1960 Jul;40:505-37. doi: 10.1152/physrev.1960.40.3.505.
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Hereditary absence of muscle phosphorylase (McArdle's syndrome).
N Engl J Med. 1961 Feb 2;264:223-5. doi: 10.1056/NEJM196102022640504.
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A metabolic myopathy due to absence of muscle phosphorylase.
Am J Med. 1961 Apr;30:502-17. doi: 10.1016/0002-9343(61)90075-4.
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[Neuromuscular form of glycogen storage disease].
Virchows Arch Pathol Anat Physiol Klin Med. 1958;331(3):287-313. doi: 10.1007/BF00955257.

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