Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- ASTROM K. E., KUGELBERG E., MULLER R. Hypothyroid myopathy. Arch Neurol. 1961 Nov;5:472–482. doi: 10.1001/archneur.1961.00450170010002. [DOI] [PubMed] [Google Scholar]
- BASTRON J. A., LAMBERT E. H., MULDER D. W. Hyperinsulin neuropathy. Neurology. 1956 Sep;6(9):627–635. doi: 10.1212/wnl.6.9.627. [DOI] [PubMed] [Google Scholar]
- BAXTER D. W., DYCK P. J. Paramyotonia congenita. Can Med Assoc J. 1961 Jul 15;85:113–118. [PMC free article] [PubMed] [Google Scholar]
- BIANCHI C. P., SHANES A. M. Calcium influx in skeletal muscle at rest, during activity, and during potassium contracture. J Gen Physiol. 1959 Mar 20;42(4):803–815. doi: 10.1085/jgp.42.4.803. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BUCHTHAL F., ENGBAEK L., GAMSTORP I. Paresis and hyperexcitability in adynamia episodica hereditaria. Neurology. 1958 May;8(5):347–351. doi: 10.1212/wnl.8.5.347. [DOI] [PubMed] [Google Scholar]
- CHAMBERS R. A., MEDD W. E., SPENCER H. Primary amyloidosis; with special reference to involvement of the nervous system. Q J Med. 1958 Apr;27(106):207–226. [PubMed] [Google Scholar]
- CREUTZFELDT O. D., ABBOTT B. C., FOWLER W. M., PEARSON C. M. MUSCLE MEMBRANE POTENTIALS IN EPISODIC ADYNAMIA. Electroencephalogr Clin Neurophysiol. 1963 Jun;15:508–519. doi: 10.1016/0013-4694(63)90071-3. [DOI] [PubMed] [Google Scholar]
- DRAGER G. A., HAMMILL J. F., SHY G. M. Paramyotonia congenita. AMA Arch Neurol Psychiatry. 1958 Jul;80(1):1–9. doi: 10.1001/archneurpsyc.1958.02340070019001. [DOI] [PubMed] [Google Scholar]
- EKBOM K., HED R., KIRSTEIN L., ASTROM K. E. MUSCULAR AFFECTIONS IN CHRONIC ALCOHOLISM. Arch Neurol. 1964 May;10:449–458. doi: 10.1001/archneur.1964.00460170019003. [DOI] [PubMed] [Google Scholar]
- ELLIS J. T. Necrosis and regeneration of skeletal muscles in cortisone-treated rabbits. Am J Pathol. 1956 Sep-Oct;32(5):993–1013. [PMC free article] [PubMed] [Google Scholar]
- ENGEL A. G. Thyroid function and periodic paralysis. Am J Med. 1961 Feb;30:327–333. doi: 10.1016/0002-9343(61)90104-8. [DOI] [PubMed] [Google Scholar]
- Eadie M. J., Ferrier T. M. Chloroquine myopathy. J Neurol Neurosurg Psychiatry. 1966 Aug;29(4):331–337. doi: 10.1136/jnnp.29.4.331. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GARLAND H. Diabetic amyotrophy. Br Med J. 1955 Nov 26;2(4951):1287–1290. doi: 10.1136/bmj.2.4951.1287. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GILLIATT R. W., WILLISON R. G. Peripheral nerve conduction in diabetic neuropathy. J Neurol Neurosurg Psychiatry. 1962 Feb;25:11–18. doi: 10.1136/jnnp.25.1.11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GLASER G. H., STARK L. Excitability in experimental myopathy. I. Measurement of refractory period; quinidine effect; cortisone myopathy. Neurology. 1958 Aug;8(8):640–644. doi: 10.1212/wnl.8.8.640. [DOI] [PubMed] [Google Scholar]
- GOLDING D. N., MURRAY S. M., PEARCE G. W., THOMPSON M. Corticosteroid myopathy. Ann Phys Med. 1961 Nov;6:171–177. doi: 10.1093/rheumatology/6.4.171. [DOI] [PubMed] [Google Scholar]
- GROB D., JOHNS R. J., LILJESTRAND A. Potassium movement in patients with familial periodic paralysis: relationship to the defect in muscle function. Am J Med. 1957 Sep;23(3):356–375. doi: 10.1016/0002-9343(57)90316-9. [DOI] [PubMed] [Google Scholar]
- HAVARD C. W., CAMPBELL E. D., ROSS H. B., SPENCE A. W. Electromyographic and histological findings in the muscles of patients with thyrotoxicosis. Q J Med. 1963 Apr;32:145–163. [PubMed] [Google Scholar]
- HED C., LUNDMARK C., FAHLGREN H., ORELL S. Acute muscular syndrome in chronic alcoholism. Acta Med Scand. 1962 May;171:585–599. doi: 10.1111/j.0954-6820.1962.tb04224.x. [DOI] [PubMed] [Google Scholar]
- HERMAN R. H., MCDOWELL M. K. HYPERKALEMIC PARALYSIS (ADYNAMIA EPISODICA HEREDITARIA). REPORT OF FOUR CASES AND CLINICAL STUDIES. Am J Med. 1963 Dec;35:749–767. doi: 10.1016/0002-9343(63)90238-9. [DOI] [PubMed] [Google Scholar]
- KOREIN J., CODDON D. R., MOWREY F. H. The clinical syndrome of paroxysmal paralytic myoglobinuria. Report of 2 cases and an analytical review of the literature. Neurology. 1959 Nov;9:767–785. doi: 10.1212/wnl.9.11.767. [DOI] [PubMed] [Google Scholar]
- LAMBERT E. H., UNDERDAHL L. O., BECKETT S., MEDEROS L. O. A study of the ankle jerk in myxedema. J Clin Endocrinol Metab. 1951 Oct;11(10):1186–1205. doi: 10.1210/jcem-11-10-1186. [DOI] [PubMed] [Google Scholar]
- LARSSON L. E., LINDERHOLM H., MUELLER R., RINGQVIST T., SOERNAES R. HEREDITARY METABOLIC MYOPATHY WITH PAROXYSMAL MYOGLOBINURIA DUE TO ABNORMAL GLYCOLYSIS. J Neurol Neurosurg Psychiatry. 1964 Oct;27:361–380. doi: 10.1136/jnnp.27.5.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LAWSON J. D. The free Achilles reflex in hypothyroidism and hyperthyroidism. N Engl J Med. 1958 Oct 16;259(16):761–764. doi: 10.1056/NEJM195810162591602. [DOI] [PubMed] [Google Scholar]
- LOCKE S., LAWRENCE D. G., LEGG M. A. Diabetic amyotrophy. Am J Med. 1963 Jun;34:775–785. doi: 10.1016/0002-9343(63)90086-x. [DOI] [PubMed] [Google Scholar]
- MCARDLE B. Familial periodic paralysis. Br Med Bull. 1956 Sep;12(3):226–229. doi: 10.1093/oxfordjournals.bmb.a069556. [DOI] [PubMed] [Google Scholar]
- MELDRUM B. S., THOMPSON R. H. The action of snake venoms on the membrane permeability of brain, muscle and red blood cells. Guys Hosp Rep. 1962;111:87–97. [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]
- MULLER R., KUGELBERG E. Myopathy in Cushing's syndrome. J Neurol Neurosurg Psychiatry. 1959 Nov;22:314–319. doi: 10.1136/jnnp.22.4.314. [DOI] [PMC free article] [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]
- OKINAKA S., SHIZUME K., IINO S., WATANABE A., IRIE M., NOGUCHI A., KUMA S., KUMA K., ITO T. The association of periodic paralysis and hyperthyroidism in Japan. J Clin Endocrinol Metab. 1957 Dec;17(12):1454–1459. doi: 10.1210/jcem-17-12-1454. [DOI] [PubMed] [Google Scholar]
- PEARCE J. M., PENNINGTON R. J., WALTON J. N. SERUM ENZYME STUDIES IN MUSCLE DISEASE. II. SERUM CREATINE KINASE ACTIVITY IN MUSCULAR DYSTROPHY AND IN OTHER MYOPATHIC AND NEUROPATHIC DISORDERS. J Neurol Neurosurg Psychiatry. 1964 Apr;27:96–99. doi: 10.1136/jnnp.27.2.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PEARSON C. M., BECK W. S., BLAHD W. H. Idiopathic paroxysmal myoglobinuria; detailed study of a case including radioisotope and serum enzyme evaluation. AMA Arch Intern Med. 1957 Mar;99(3):376–389. doi: 10.1001/archinte.1957.00260030056006. [DOI] [PubMed] [Google Scholar]
- PEARSON C. M., RIMER D. G., MOMMAERTS W. F. A metabolic myopathy due to absence of muscle phosphorylase. Am J Med. 1961 Apr;30:502–517. doi: 10.1016/0002-9343(61)90075-4. [DOI] [PubMed] [Google Scholar]
- PEARSON C. M., YAMAZAKI J. N. Vacuolar myopathy in systemic lupus erythematosus. Am J Clin Pathol. 1958 May;29(5):455–463. doi: 10.1093/ajcp/29.5.455. [DOI] [PubMed] [Google Scholar]
- PERKOFF G. T., SILBER R., TYLER F. H., CARTWRIGHT G. E., WINTROBE M. M. Studies in disorders of muscle. XII. Myopathy due to the administration of therapeutic amounts of 17-hydroxycorticosteroids. Am J Med. 1959 Jun;26(6):891–898. doi: 10.1016/0002-9343(59)90211-6. [DOI] [PubMed] [Google Scholar]
- POSKANZER D. C., KERR D. N. A third type of periodic paralysis, with normokalemia and favourable response to sodium chloride. Am J Med. 1961 Sep;31:328–342. doi: 10.1016/0002-9343(61)90122-x. [DOI] [PubMed] [Google Scholar]
- POSKANZER D. C., KERR D. N. Periodic paralysis with response to spironolactone. Lancet. 1961 Sep 2;2(7201):511–513. doi: 10.1016/s0140-6736(61)92954-3. [DOI] [PubMed] [Google Scholar]
- PRINEAS J. W., MASON A. S., HENSON R. A. MYOPATHY IN METABOLIC BONE DISEASE. Br Med J. 1965 Apr 17;1(5441):1034–1036. doi: 10.1136/bmj.1.5441.1034. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perkoff G. T., Hardy P., Velez-Garcia E. Reversible acute muscular syndrome in chronic alcoholism. N Engl J Med. 1966 Jun 9;274(23):1277–1285. doi: 10.1056/NEJM196606092742301. [DOI] [PubMed] [Google Scholar]
- REID H. A. Myoglobinuria and sea-snake-bite poisoning. Br Med J. 1961 May 6;1(5235):1284–1289. doi: 10.1136/bmj.1.5235.1284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ramsay I. D. Electromyography in thyrotoxicosis. Q J Med. 1965 Jul;34(135):255–267. [PubMed] [Google Scholar]
- Ramsay I. D. Muscle dysfunction in hyperthyroidism. Lancet. 1966 Oct 29;2(7470):931–934. doi: 10.1016/s0140-6736(66)90536-8. [DOI] [PubMed] [Google Scholar]
- Rowland L. P., Lovelace R. E., Schotland D. L., Araki S., Carmel P. The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase. Neurology. 1966 Jan;16(1):93–100. doi: 10.1212/wnl.16.1.93. [DOI] [PubMed] [Google Scholar]
- SAMAHA F. J. HYPERKALEMIC PERIODIC PARALYSIS. A GENETIC STUDY, CLINICAL OBSERVATIONS, AND REPORT OF A NEW METHOD OF THERAPY. Arch Neurol. 1965 Feb;12:145–154. doi: 10.1001/archneur.1965.00460260035004. [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]
- SMITH B. HISTOLOGICAL AND HISTOCHEMICAL CHANGES IN THE MUSCLES OF RABBITS GIVEN THE CORTICOSTEROID TRIAMCINOLONE. Neurology. 1964 Sep;14:857–863. doi: 10.1212/wnl.14.9.857. [DOI] [PubMed] [Google Scholar]
- Schotland D. L., Spiro D., Rowland L. P., Carmel P. Ultrastructural studies of muscle in McArdle's disease. J Neuropathol Exp Neurol. 1965 Oct;24(4):629–644. doi: 10.1097/00005072-196510000-00006. [DOI] [PubMed] [Google Scholar]
- Shy G. M., Gonatas N. K., Perez M. Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy. Brain. 1966 Mar;89(1):133–158. doi: 10.1093/brain/89.1.133. [DOI] [PubMed] [Google Scholar]
- Smith B., O'Grady F. Experimental chloroquine myopathy. J Neurol Neurosurg Psychiatry. 1966 Jun;29(3):255–258. doi: 10.1136/jnnp.29.3.255. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TARUI S., OKUNO G., IKURA Y., TANAKA T., SUDA M., NISHIKAWA M. PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS. Biochem Biophys Res Commun. 1965 May 3;19:517–523. doi: 10.1016/0006-291x(65)90156-7. [DOI] [PubMed] [Google Scholar]
- TYLER F. H., STEPHENS F. E., GUNN F. D., PERKOFF G. T. Studies in disorders of muscle. VII. Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia. J Clin Invest. 1951 May;30(5):492–502. doi: 10.1172/JCI102465. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WHISNANT J. P., ESPINOSA R. E., KIERLAND R. R., LAMBERT E. H. CHLOROQUINE NEUROMYOPATHY. Proc Staff Meet Mayo Clin. 1963 Nov 6;38:501–513. [PubMed] [Google Scholar]
- WILSON J., WALTON J. N. Some muscular manifestations of hypothyroidism. J Neurol Neurosurg Psychiatry. 1959 Nov;22:320–324. doi: 10.1136/jnnp.22.4.320. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ZIERLER K. L., ANDRES R. Movement of potassium into skeletal muscle during spontaneous attack in family periodic paralysis. J Clin Invest. 1957 May;36(5):730–737. doi: 10.1172/JCI103476. [DOI] [PMC free article] [PubMed] [Google Scholar]