Full text
PDF











Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- ANDRES R., CADER G., ZIERLER K. L. The quantitatively minor role of carbohydrate in oxidative metabolism by skeletal muscle in intact man in the basal state; measurements of oxygen and glucose uptake and carbon dioxide and lactate production in the forearm. J Clin Invest. 1956 Jun;35(6):671–682. doi: 10.1172/JCI103324. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BAKER R. W., EVANS J. H. Serum aldolase and the diagnosis of myopathy. Brain. 1957 Dec;80(4):557–570. doi: 10.1093/brain/80.4.557. [DOI] [PubMed] [Google Scholar]
- BRODY I. A. THE SIGNIFICANCE OF LACTATE DEHYDROGENASE ISOZYMES IN ABNORMAL HUMAN SKELETAL MUSCLE. Neurology. 1964 Dec;14:1091–1100. doi: 10.1212/wnl.14.12.1091. [DOI] [PubMed] [Google Scholar]
- DAWSON D. M., GOODFRIEND T. L., KAPLAN N. O. LACTIC DEHYDROGENASES: FUNCTIONS OF THE TWO TYPES RATES OF SYNTHESIS OF THE TWO MAJOR FORMS CAN BE CORRELATED WITH METABOLIC DIFFERENTIATION. Science. 1964 Feb 28;143(3609):929–933. doi: 10.1126/science.143.3609.929. [DOI] [PubMed] [Google Scholar]
- DE MORAGAS J. M., PERRY H. O., FLEISHER G. A. Serum glutamic oxalacetic transaminase in dermatomyositis. J Am Med Assoc. 1957 Dec 14;165(15):1936–1938. doi: 10.1001/jama.1957.02980330038009. [DOI] [PubMed] [Google Scholar]
- DEMOS J., DREYFUS J. C., SCHAPIRA F., SCHAPIRA G. Activités enzymatiques du muscle humain; recherches sur la biochimie comparée de l'homme normal et myopathique, et du rat. Clin Chim Acta. 1956 Sep-Oct;1(5):434–449. doi: 10.1016/0009-8981(56)90016-x. [DOI] [PubMed] [Google Scholar]
- DREYFUS J. C., SCHAPIRA G., SCHAPIRA F. Serum enzymes in the physiopathology of muscle. Ann N Y Acad Sci. 1958 Oct 13;75(1):235–249. doi: 10.1111/j.1749-6632.1958.tb36870.x. [DOI] [PubMed] [Google Scholar]
- DUBOWITZ V., PEARSE A. G. A comparative histochemical study of oxidative enzyme and phosphorylase activity in skeletal muscle. Z Zellforch Microsk Anat Histochem. 1960;2:105–117. doi: 10.1007/BF00744575. [DOI] [PubMed] [Google Scholar]
- DUBOWITZ V. Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance. Brain. 1960 Sep;83:432–439. doi: 10.1093/brain/83.3.432. [DOI] [PubMed] [Google Scholar]
- EMERY A. E. ELECTROPHORETIC PATTERN OF LACTIC DEHYDROGENASE IN CARRIERS AND PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY. Nature. 1964 Mar 7;201:1044–1045. doi: 10.1038/2011044a0. [DOI] [PubMed] [Google Scholar]
- FOWLER W. M., Jr, CHOWDHURY S. R., PEARSON C. M., GARDNER G., BRATTON R. Changes in serum enzyme levels after exercise in trained and untrained subjects. J Appl Physiol. 1962 Nov;17:943–946. doi: 10.1152/jappl.1962.17.6.943. [DOI] [PubMed] [Google Scholar]
- FOWLER W. M., Jr, PEARSON C. M. DIAGNOSTIC AND PROGNOSTIC SIGNIFICANCE OF SERUM ENZYMES. II. NEUROLOGIC DISEASES OTHER THAN MUSCULAR DYSTROPHY. Arch Phys Med Rehabil. 1964 Mar;45:125–130. [PubMed] [Google Scholar]
- FRIEDMAN M. M., LAPAN B. Serum aldolase in the neonatal period: including a colorimetric determination of aldolase by standardization with dihydroxyacetone. J Lab Clin Med. 1958 May;51(5):745–752. [PubMed] [Google Scholar]
- FRITZ I. B., DAVIS D. G., HOLTROP R. H., DUNDEE H. Fatty acid oxidation by skeletal muscle during rest and activity. Am J Physiol. 1958 Aug;194(2):379–386. doi: 10.1152/ajplegacy.1958.194.2.379. [DOI] [PubMed] [Google Scholar]
- GRIFFITHS P. D. Creatinephosphokinase levels in hypothyroidism. Lancet. 1963 Apr 20;1(7286):894–894. doi: 10.1016/s0140-6736(63)91676-3. [DOI] [PubMed] [Google Scholar]
- HALONEN P. I., KONTTINEN A. Effect of physical exercise on some enzymes in the serum. Nature. 1962 Mar 10;193:942–944. doi: 10.1038/193942a0. [DOI] [PubMed] [Google Scholar]
- HOCKADAY T. D., DOWNEY J. A., MOTTRAM R. F. A CASE OF MCARDLE'S SYNDROME WITH A POSITIVE FAMILY HISTORY. J Neurol Neurosurg Psychiatry. 1964 Jun;27:186–197. doi: 10.1136/jnnp.27.3.186. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HUGHES B. P. A method for the estimation of serum creatine kinase and its use in comparing creatine kinase and aldolase activity in normal and pathological sera. Clin Chim Acta. 1962 Sep;7:597–603. doi: 10.1016/0009-8981(62)90137-7. [DOI] [PubMed] [Google Scholar]
- HUGHES B. P. Serum enzyme changes in muscle disease and their relation to tissue change. Proc R Soc Med. 1963 Mar;56:179–182. doi: 10.1177/003591576305600318. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LYON M. F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. doi: 10.1038/190372a0. [DOI] [PubMed] [Google Scholar]
- Larner J., Villar-Palasi C. ENZYMES IN A GLYCOGEN STORAGE MYOPATHY. Proc Natl Acad Sci U S A. 1959 Aug;45(8):1234–1235. doi: 10.1073/pnas.45.8.1234. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MELLICK R. S., MAHLER R. F., HUGHES B. P. McArdle's syndrome: phosphorylase-deficient myopathy. Lancet. 1962 May 19;1(7238):1045–1048. doi: 10.1016/s0140-6736(62)92145-1. [DOI] [PubMed] [Google Scholar]
- Mommaerts W. F., Illingworth B., Pearson C. M., Guillory R. J., Seraydarian K. A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE. Proc Natl Acad Sci U S A. 1959 Jun;45(6):791–797. doi: 10.1073/pnas.45.6.791. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PEARSON C. M. THE PERIODIC PARALYSES: DIFFERENTIAL FEATURES AND PATHOLOGICAL OBSERVATIONS IN PERMANENT MYOPATHIC WEAKNESS. Brain. 1964 Jun;87:341–354. doi: 10.1093/brain/87.2.341. [DOI] [PubMed] [Google Scholar]
- PLUMMER D. T., ELLIOTT B. A., COOKE K. B., WILKINSON J. H. Organ specificity and lactate-dehydrogenase activity. 1. The relative activities with pyruvate and 2-oxobutyrate of electrophoretically separated fractions. Biochem J. 1963 May;87:416–422. doi: 10.1042/bj0870416. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROWLAND L. P., FAHN S., SCHOTLAND D. L. MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE. Arch Neurol. 1963 Oct;9:325–342. doi: 10.1001/archneur.1963.00460100013001. [DOI] [PubMed] [Google Scholar]
- Richterich R., Rosin S., Aebi U., Rossi E. Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination. Am J Hum Genet. 1963 Jun;15(2):133–154. [PMC free article] [PubMed] [Google Scholar]
- SCHLANG H. A. The effect of physical exercise on serum transaminase. Am J Med Sci. 1961 Sep;242:338–341. doi: 10.1097/00000441-196109000-00009. [DOI] [PubMed] [Google Scholar]
- SCHMID R., HAMMAKER L. Hereditary absence of muscle phosphorylase (McArdle's syndrome). N Engl J Med. 1961 Feb 2;264:223–225. doi: 10.1056/NEJM196102022640504. [DOI] [PubMed] [Google Scholar]
- SCHMID R., MAHLER R. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle. J Clin Invest. 1959 Nov;38:2044–2058. doi: 10.1172/JCI103983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SIBLEY J. A., LEHNINGER A. L. Aldolase in the serum and tissue of tumor-bearing animals. J Natl Cancer Inst. 1949 Feb;9(4):303–309. [PubMed] [Google Scholar]
- SOLVONUK P. F., MCRAE S. C., COLLIER H. B. Creatine phosphokinase activity of mammalian erythrocytes. Can J Biochem Physiol. 1956 May;34(3):481–487. [PubMed] [Google Scholar]
- SUTHERLAND E. W., WOSILAIT W. D. The relationship of epinephrine and glucagon to liver phosphorylase. I. Liver phosphorylase; preparation and properties. J Biol Chem. 1956 Jan;218(1):459–468. [PubMed] [Google Scholar]
- THOMPSON R. A., VIGNOS P. J., Jr Serum aldolase in muscle disease. AMA Arch Intern Med. 1959 Apr;103(4):551–564. doi: 10.1001/archinte.1959.00270040037004. [DOI] [PubMed] [Google Scholar]
- THOMSON W. A. Sources of error in the biochemical diagnosis of muscular dystrophy. J Neurol Neurosurg Psychiatry. 1962 Aug;25:191–202. doi: 10.1136/jnnp.25.3.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
- THOMSON W. H., LEYBURN P., WALTON J. N. Serum enzyme activity in muscular dystrophy. Br Med J. 1960 Oct 29;2(5208):1276–1281. doi: 10.1136/bmj.2.5208.1276. [DOI] [PMC free article] [PubMed] [Google Scholar]
- VAN PILSUM J. F., WOLIN E. A. Guanidinium compounds in blood and urine of patients suffering from muscle disorders. J Lab Clin Med. 1958 Feb;51(2):219–223. [PubMed] [Google Scholar]
- VIGNOS P. J., Jr, LEFKOWITZ M. A biochemical study of certain skeletal muscle constituents in human progressive muscular dystrophy. J Clin Invest. 1959 Jun;38(6):873–881. doi: 10.1172/JCI103869. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WILSON K. M., EVANS K. A., CARTER C. O. CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY. Br Med J. 1965 Mar 20;1(5437):750–753. doi: 10.1136/bmj.1.5437.750. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ZIERLER K. L. Increased muscle permeability to aldolase produced by depolarization and by metabolic inhibitors. Am J Physiol. 1958 Jun;193(3):534–538. doi: 10.1152/ajplegacy.1958.193.3.534. [DOI] [PubMed] [Google Scholar]