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Sources of error in the biochemical diagnosis of muscular dystrophy.

作者信息

THOMSON W A

出版信息

J Neurol Neurosurg Psychiatry. 1962 Aug;25(3):191-202. doi: 10.1136/jnnp.25.3.191.

DOI:10.1136/jnnp.25.3.191
PMID:14037852
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC495443/
Abstract
摘要

相似文献

1
Sources of error in the biochemical diagnosis of muscular dystrophy.肌营养不良生化诊断中的误差来源。
J Neurol Neurosurg Psychiatry. 1962 Aug;25(3):191-202. doi: 10.1136/jnnp.25.3.191.
2
[The significance of serum enzymes in the early diagnosis of progressive muscular dystrophy].
Monatsschr Kinderheilkd (1902). 1965 Jul;113(7):481-6.
3
[Diagnosis of progressive muscular dystrophy].[进行性肌营养不良症的诊断]
Maandschr Kindergeneeskd. 1970 Feb;37(10):293-311.
4
Early muscular dystrophy: differential patterns of weakness in duchenne, limb-girdle and facioscapulohumeral types.
Arch Phys Med Rehabil. 1966 Aug;47(8):499-503.
5
[Enzyme diagnosis in progressive muscular dystrophies, especially in the Duchenne type].[进行性肌营养不良症的酶诊断，尤其是杜兴型]
Klin Padiatr. 1989 May-Jun;201(3):167-76. doi: 10.1055/s-2007-1025297.
6
[Progressive muscular dystrophy. VII. Detection of heterozygotes of Duehenne muscular dystrophy by determining serum creatine kinase with localized work load in anoxia].[进行性肌营养不良症。VII. 通过在缺氧状态下进行局部负荷测定血清肌酸激酶来检测杜兴氏肌营养不良症的杂合子]
Klin Wochenschr. 1965 Oct 1;43(19):1015-22. doi: 10.1007/BF01746589.
7
[Progressive muscular dystrophy. III. Serum enzymes in muscular dystrophy in childhood].[进行性肌营养不良。III. 儿童期肌营养不良中的血清酶]
Helv Paediatr Acta. 1961 Dec;16:543-64.
8
Restricted myositis with myoedema simulating facioscapulohumeral muscular dystrophy.伴有肌水肿的局限性肌炎，酷似面肩肱型肌营养不良症。
Neurology. 1970 Apr;20(4):386-7.
9
[Creatine phosphokinase in differential diagnosis of muscular dystrophies].
G Clin Med. 1965 Feb;46(2):155-64.
10
Some alterations in serum enzymes in progressive muscular dystrophy.
Proc Soc Exp Biol Med. 1957 Mar;94(3):541-4. doi: 10.3181/00379727-94-23006.

引用本文的文献

1
Some Biochemical Aspects of the Myopathies.肌病的一些生化方面
Postgrad Med J. 1965 Jun;41(476):313-24. doi: 10.1136/pgmj.41.476.313.
2
SERUM ENZYME VARIATIONS AND HISTOLOGICAL ABNORMALITIES IN THE CARRIER STATE IN DUCHENNE DYSTROPHY.杜氏肌营养不良症携带者状态下的血清酶变化及组织学异常
J Neurol Neurosurg Psychiatry. 1965 Apr;28(2):104-8. doi: 10.1136/jnnp.28.2.104.
3
[CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. I. SERUM ENZYMES IN PROGRESSIVE MUSCULAR DYSTROPHY (TYPE I, II, IIIA)].[肌病的临床与生化研究。I. 进行性肌营养不良（I型、II型、IIIA型）中的血清酶]
Klin Wochenschr. 1965 Feb 1;43:144-50. doi: 10.1007/BF01484506.
4
LAEVADOSIN FOR MUSCULAR DYSTROPHY.左多巴辛用于治疗肌肉萎缩症。
Br Med J. 1964 Oct 31;2(5417):1135-6. doi: 10.1136/bmj.2.5417.1135-d.
5
UNDESCENDED TESTES.
Indian J Pediatr. 1964 May;31:159-60. doi: 10.1007/BF02748438.
6
SERUM ENZYME STUDIES IN MUSCLE DISEASE. II. SERUM CREATINE KINASE ACTIVITY IN MUSCULAR DYSTROPHY AND IN OTHER MYOPATHIC AND NEUROPATHIC DISORDERS.肌肉疾病的血清酶研究。II. 肌营养不良症以及其他肌病和神经病性疾病中的血清肌酸激酶活性
J Neurol Neurosurg Psychiatry. 1964 Apr;27(2):96-9. doi: 10.1136/jnnp.27.2.96.
7
A trial of therapy by nucleosides and nucleotides in muscular dystrophy.核苷和核苷酸治疗肌肉萎缩症的试验。
J Neurol Neurosurg Psychiatry. 1963 Apr;26(2):111-22. doi: 10.1136/jnnp.26.2.111.
8
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.
9
Serum enzyme changes in muscle disease and their relation to tissue change.肌肉疾病中的血清酶变化及其与组织变化的关系。
Proc R Soc Med. 1963 Mar;56(3):179-82. doi: 10.1177/003591576305600318.
10
Enzymes of the glycogen cycle and glycolysis in various human neuromuscular disorders.各种人类神经肌肉疾病中糖原循环和糖酵解的酶。
J Neurol Neurosurg Psychiatry. 1967 Oct;30(5):411-5. doi: 10.1136/jnnp.30.5.411.

本文引用的文献

1
Myotonia congenita, dystrophia myotonica and paramyotonia; reaffirmation of their identity.先天性肌强直、强直性肌营养不良症和发作性肌强直；对它们特征的再次确认。
Brain. 1950;73(3):318-36. doi: 10.1093/brain/73.3.318.
2
The molecular turnover of muscle aldolase.肌肉醛缩酶的分子更新
J Biol Chem. 1960 Jun;235:1738-41.
3
[Changes in serum glutamic oxalacetic transaminases and aldolases in muscle diseases, with special reference to Steinert's myotonic dystrophy].
Riv Patol Nerv Ment. 1959;80:1-12.
4
Multiple serial enzyme studies in acute myocardial infarction.急性心肌梗死的多项系列酶学研究。
Br Med J. 1959 Sep 19;2(5150):459-63. doi: 10.1136/bmj.2.5150.459.
5
A comparative study of fetal and maternal serum enzyme levels.
J Lab Clin Med. 1959 Sep;54:417-26.
6
Abnormalities of muscle protein metabolism in mice with muscular dystrophy.患有肌肉萎缩症的小鼠肌肉蛋白质代谢异常。
J Clin Invest. 1960 Jul;39(7):1180-4. doi: 10.1172/JCI104132.
7
[The behavior of serum glutamic acid-oxalacetic acid transaminase in myopathies and neurogenic muscle atrophies].[血清谷氨酸草酰乙酸转氨酶在肌病和神经源性肌肉萎缩中的表现]
Dtsch Z Nervenheilkd. 1959;179:353-62.
8
Muscular dystrophy in three pairs of twins.
Acta Genet Med Gemellol (Roma). 1959 Oct;8:434-42. doi: 10.1017/s1120962300018618.
9
[Significance of the increase of aldolase in blood in muscular dystrophy].
Clin Pediatr (Bologna). 1959 Sep;41:736-9.
10
[On the problem of the pathogenesis of muscular atrophy in chronic polyarthritis].
Z Rheumaforsch. 1959 Dec;18:455-9.