The DOI matches its Crossref record.
The essentiality of histo- and cytochemical studies of skeletal muscle in the investigation of neuromuscular disease
Abstract
American Academy of Neurology Dedicated to advancing the art and science of neurology, and thereby promoting the best possible care for patients with neurological disorders A Celebration of the First 50 years of the American Academy of Neurology Neurology 1962;12:778-794 In the investigation of neuromuscular disease, histologic examination of skeletal muscle biopsies is generally accepted as an important part both of routine diagnostic procedures and of more specialized research. The purpose of the present report is to establish that the use of histo- and cytochemical technics combined with light microscopy is also an essential aspect of both types of investigation. Substantiating evidence is presented in the form of 6 examples, chosen from recent studies, of cytopathologic changes in neuromuscular disease as demonstrated by these technics. Two fundamental types of abnormalities in skeletal muscle are detectable with histo- and cytochemical technics: (a) a generalized change of a given reaction, for example, loss of phosphorylase activity, and (b) a localized change of activity confined either to a specific type of muscle fiber (as in the new myopathy with rod-shaped structures) or to certain regions of individual muscle fibers (as in target fibers and central core disease). Further, if the cytochemical technics are sufficiently refined, they may be used to demonstrate the functional activity of fine structural components of the muscle cell. On the basis of such data, predictions can often be made as to the fine structural changes which electron-microscopy will reveal. It must be understood, though, that some cytochemical changes might not be accompanied by changes of fine structure and vice versa. Cytochemistry combined with electron-microscopy would give even more detailed information, but this approach has 2 major limitations: (a) only a very few cytochemical reactions are as yet refined enough to be used with electron-microscopy and(b) study of a large …
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
No references could be resolved yet.
Research works printed but not linked: 50
- Dubowitz V. and Pearse A. G. E.: Oxidative enzymes and phosphorylase in central core disease of muscle. Lancet 2:23 1960. · DOI
- Dubowitz V. and Pearse A. G. E.: Enzymatic activity of normal and dystrophic human muscle: a histochemical study. J. Path. Bact. 81:365 1961. · doi:10.1002/path.1700810208
- Beckett E. B. and Bourne G. H.: Histochemistry of skeletal muscle and changes in some muscle diseases in Structure and Function of Muscle Bourne G. H. ed. vol. III. New York Academic Press 1960 pp. 276-320.
- Bourne G. H. and Golarz M. N.: Human muscular dystrophy as an aberration of the connective tissue. Nature 183:1741 1959. · doi:10.1038/1831741a0
- Golarz M. N. Bourne G. H. and Richardson H. D.: Histochemical studies on human muscular dystrophy. J. Histochem. Cytochem. 9:132 1961. · doi:10.1177/9.2.132
- Engel W. K.: Muscle target fibers a newly recognized sign of denervation. Nature 191:389 1961. · doi:10.1038/191389a0
- Nachlas M. M. Tsou K. C. De Souza E. Cheng C. S. and Seligman A. M.: Cytochemical demonstration of succinate dehydrogenase by the use of a new p-nitrophenyl substituted ditetrazole. J. Histochem. Cytochem. 5:420 1957. · DOI · Paper page
- Novikoff A. B. Shin W.-Y. and Drucker J.: Mitochondrial localization of oxidative enzymes: staining results with two tetrazolium salts. J. Biophys. Biochem. Cytol. 9:47 1961. · DOI · Paper page
- Hess R. Scarpelli D. G. and Pearse A. G. E.: The cytochemical localization of oxidative enzymes. II. Pyridine nucleotide-linked dehydrogenases. J. Biophys. Biochem. Cytol. 4:735 1958. · doi:10.1038/1811531a0
- Wattenberg L. W. and Leong J. L.: Effects of coenzyme Q 10 and menadione on succinic dehydrogenase activity as measured by tetrazolium salt reduction. J. Histochem. Cytochem. 8:296 1960. · DOI · Paper page
- Burstone M. S.: Histochemical demonstration of cytochrome oxidase with new amine reagents. J. Histochem. Cytochem. 8:63 1960. · DOI
- Takeuchi T.: Histochemical demonstration of branching enzyme (amylo-1 4→1 6-transglucosidase) in animal tissues. J. Histochem. Cytochem. 6:208 1958. · DOI
- Takeuchi T. and Glenner G. G.: Histochemical demonstration of uridine diphosphate glucose-glycogen transferase in animal tissues. J. Histochem. Cytochem. 9:304 1961. · doi:10.1177/9.3.304
- Padykuda H. A. and Herman E.: The specificity of the histochemical method for adenosine triphosphatase. J. Histochem. Cytochem. 3:170 1955. · DOI · Paper page
- Shy G. M. Engel W. K. and Wanko T.: Central core disease. Ann. Int. Med. 56:511 1962. · doi:10.7326/0003-4819-56-3-511
- Veratti E.: Investigations of the fine structure of striated muscle fiber. J. Biophys. Biochem. Cytol. 10: in suppl. The Sarcoplasmic Reticulum 1961 p. 1. · doi:10.1083/jcb.10.4.1
- Andersson-Cedergren E.: Ultrastructure of motor end plate and sarcoplasmic components of mouse skeletal muscle fiber. J. Ultrastruct. Res. suppl. 1959 p. 1. · DOI · Paper page
- Porter K. R.: The sarcoplasmic reticulum; its recent history and present status. J. Biophys. Biochem. Cytol. 10: in suppl. The Sarcoplasmic Reticulum 1961 p. 219. · doi:10.1083/jcb.10.4.219
- Tunik B. and Holtzer H.: The distribution of muscle antigens in contracted myofibrils determined by fluorescein-labeled antibodies. J. Biophys. Biochem. Cytol. 11:67 1961. · doi:10.1083/jcb.11.1.67
- Engel W. K. and Horvath B.: Myofibril formation in cultured skeletal muscle cells studied with antimyosin fluorescent antibody. J. Exp. Zool. 144:209 1960. · doi:10.1002/jez.1401440302
- Fawcett D. W. and Revel J. P.: The sarcoplasmic reticulum of a fast-acting fish muscle. J. Biophys. Biochem. Cytol. 10: in suppl. The Sarcoplasmic Reticulum 1961 p. 89. · DOI · Paper page
- Smith D. S.: The structure of insect fibrillar flight muscle. A study made with special reference to the membrane systems of the fiber. J. Biophys. Biochem. Cytol. 10: in suppl. The Sarcoplasmic Reticulum 1961 p. 123. · DOI · Paper page
- Denny-Brown D. E.: The histological features of striped muscle in relation to its functional activity. Proc. Roy. Soc.(London) ser. B 104:371 1929. · DOI · Paper page
- Nachmias V. T. and Padykula H. A.: A histochemical study of normal and denervated red and white muscles of the rat. J. Biophys. Biochem. Cytol. 4:47 1958. · doi:10.1083/jcb.4.1.47
- Dubowitz V. and Pearse A. G. E.: Reciprocal relationship of phosphorylase and oxidative enzymes in skeletal muscle. Nature 185:701 1960. · DOI · Paper page
- Dubowitz V. and Pearse A. G. E.: A comparative histochemical study of oxidative enzyme and phosphorylase activity in skeletal muscle. Histochemie 2: 105 1960. · DOI · Paper page
- Pearse A. G. E.: Direct relationship of phosphorylase and mitochondrial alpha-glycerophosphate dehydrogenase activity in skeletal muscle. Nature 191:504 1961. · doi:10.1038/191504a0
- Hess R. and Pearse A. G. E.: Dissociation of uridine diphosphate glucose-glycogen transglucosylase from phosphorylase activity in individual muscle fibers. Proc. Soc. Exper. Biol. & Med. 107:569 1961. · doi:10.3181/00379727-107-26690
- Schmid R. and Mahler R.: Chronic progressive myopathy with myoglobinuria; demonstration of a glycogenolytic defect in the muscle. J. Clin. Invest. 38: 2044 1959. · doi:10.1172/jci103983
- Schmid R. Robbins P. W. and Traut R.: Glycogen synthesis in muscle lacking phosphorylase. Proc. Nat. Acad. Sci. (USA) 45:1236 1959. · doi:10.1073/pnas.45.8.1236
- Larner J. and Villar-Palasi C.: Enzymes in a glycogen storage myopathy. Proc. Nat. Acad. Sci. (USA) 45:1234 1959. · doi:10.1073/pnas.45.8.1234
- Robbins P. W.: Immunological study of human muscle lacking phosphorylase. Fed. Proc. 19:193 1960.
- Schmid R. and Hammaker L.: Hereditary absence of muscle phosphorylase (McArdle's syndrome). New England J. Med. 264:223 1961. · doi:10.1056/nejm196102022640504
- Pearson C. M. Rimer D. G. and Mommaerts W. F. H. M.: Defect in muscle phosphorylase: a newly defined human disease. Clin. Res. 7:298 1959.
- Mommaerts W. F. H. M. Illingworth B. Pearson C. M. Guillory R. J. and Seraydarian K.: A functional disorder of muscle associated with the absence of phosphorylase. Proc. Nat. Acad. Sci. (USA) 45:791 1959. · DOI
- Pearson C. M. Rimer D. G. and Mommaerts W. F. H. M.: A metabolic myopathy due to absence of muscle phosphorylase. Am. J. Med. 30:502 1961. · doi:10.1016/0002-9343(61)90075-4
- Engel W. K. Foster J. B. Hughes B. P. Huxley H. E. and Mahler R.: Central core disease-an investigation of a rare muscle cell abnormality. Brain 84:167 1961. · doi:10.1093/brain/84.2.167
- Shy G. M. and Magee K. R.: A new congenital nonprogressive myopathy. Brain 79:610 1956. · DOI · Paper page
- Seitelberger F. Wanko T. and Gavin M. A.: The muscle fiber in central core disease. Histochemical and electron microscopic observations. Acta Neuropath. 1:223 1961. · doi:10.1007/bf00687189
- Tower S. S.: Atrophy and degeneration in skeletal muscle. Am. J. Anat. 56:1 1935. · doi:10.1002/aja.1000560102
- Mumenthaler M. and Engel W. K.: Cytological localization of cholinesterase in developing chick embryo skeletal muscle. Acta anat. 47:274 1961. · DOI
- Engel W. K.: Cytological localization of cholinesterase in cultured skeletal muscle cells. J. Histochem. Cytochem. 9:66 1961. · doi:10.1177/9.1.66
- Engel W. K.: Cytological localization of glycogen in cultured skeletal muscle. J. Histochem. Cytochem. 9:38 1961. · doi:10.1177/9.1.38
- Wohlfart G.: Dystrophia myotonica and myotonia congenita. Histopathologic studies with special reference to changes in the muscles. J. Neuropath. Exper. Neurol. 10:109 1951. · doi:10.1097/00005072-195104000-00001
- Adams R. D. Denny-Brown D. and Pearson C. M.: Diseases of Muscle. A Study in Pathology. New York Paul B. Hoeber 1954 p. 462.
- Engel W. K.: Chemocytology of striated annulets and sarcoplasmic masses in myotonic dystrophy. J. Histochem. Cytochem. 10:229 1962. · doi:10.1177/10.2.229
- Whorton C. M. Hudgins P. C. and Conners J. J.: Abnormal spectrophotometric absorption spectrums of myoglobin in two forms of progressive muscular dystrophy. New England J. Med. 265:1242 1961. · DOI
- Drews G. A. and Engel W. K.: An attempt at histochemical localization of myoglobin in skeletal muscle by the benzidine-peroxidase reaction. J. Histochem. Cytochem. 9:206 1961. · doi:10.1177/9.2.206
- Buller A. J. Eccles J. C. and Eccles R. M.: Differentiation of fast and slow muscles in the cat hind limb. J. Physiol. 150:399 1960. · DOI · Paper page
- Buller A. J. Eccles J. C. and Eccles R. M.: Interactions between motoneurones and muscles in respect of the characteristic speeds of their responses. J. Physiol. 150:417 1960. · DOI · Paper page
Cited by
Skeletal Muscle Fiber Type: Influence on Contractile and Metabolic Properties
Zierath, J. R., & Hawley, J. A. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020348 · Cited by 518
Muscle Fibre Type Populations of Human Leg Muscles
Edgerton, V. R., Smith, J. L., & Simpson, D. R. (1975) · The Histochemical Journal · doi:10.1007/bf01003594 · Cited by 494
EMG frequency spectrum, muscle structure, and fatigue during dynamic contractions in man
Komi, P. V., & Tesch, P. (1979) · European Journal of Applied Physiology and Occupational Physiology · doi:10.1007/bf00421103 · Cited by 461
Skeletal muscle fibres as factors for pork quality
Karlsson, A. H., Klont, R. E., & Fernandez, X. (1999) · Livestock Production Science · doi:10.1016/s0301-6226(99)00098-6 · Cited by 289
Neuromuscular Disease in Primary Hyperparathyroidism
PATTEN, B. M., BILEZIKIAN, J. P., MALLETTE, L. E., PRINCE, A., ENGEL, W. K., & AURBACH, G. D. (1974) · Annals of Internal Medicine · doi:10.7326/0003-4819-80-2-182 · Cited by 272
Self-citation
Metadata
- Authors
- Engel, W. K.
- Venue
- Neurology
- Published
- 1998-09
- Volume
- 51
- Issue
- 3
- Pages
- 778-794
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W2118636926
- Cited by
- 333
- References
- 0
- FWCI
- 1.24
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: The essentiality of histo- and cytochemical studies of skeletal muscle in the investigation of neuromuscular disease. https://app.cochat.ai/papers/10.1212/wnl.51.3.778
- The paper
- Engel, W. K. (1998). The essentiality of histo- and cytochemical studies of skeletal muscle in the investigation of neuromuscular disease. Neurology. https://doi.org/10.1212/wnl.51.3.778
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.