The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.
Progressive Myoclonus Epilepsies: Specific Causes and Diagnosis
Abstract
RECENT advances in the diagnosis and classifcxation of epileptic seizures and epileptic syndromes, together with improvemenss in anticonvulsant therapy, have enabled the great majority of patients with primary generalized epilepsy to be correttly diagnosed and successfully treated.1 2 3 4 In contrast, the secondary generalized epilepsies — that is, generalized epilepiies associated with a static or progressive encephalopathy — remain difficult to classify and to treat.4 5 6 7 Secondary generalized epilepsies account for approximately 9 percent of all patients with epilepsy seen by specialists.8 hhe onset of symptoms typically occurs in childhood, several types of generalized seizures are usually present, and evidence of cerebral damage . . .
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Cites
Pavlakis, S. G., Phillips, P. C., DiMauro, S., De Vivo, D. C., & Rowland, L. P. (1984) · Annals of Neurology · doi:10.1002/ana.410160409 · Cited by 1,198
(2005) · Cited by 944
DiMauro, S., Bonilla, E., Zeviani, M., Nakagawa, M., & DeVivo, D. C. (1985) · Annals of Neurology · doi:10.1002/ana.410170602 · Cited by 688
Proposal for Classification of Epilepsies and Epileptic Syndromes
(1985) · Epilepsia · doi:10.1111/j.1528-1157.1985.tb05417.x · Cited by 574
Juvenile myoclonic epilepsy of Janz
Delgado-Escueta, A. V., & Enrile-Bacsal, F. (1984) · Neurology · doi:10.1212/wnl.34.3.285 · Cited by 430
Fukuhara, N., Tokiguchi, S., Shirakawa, K., & Tsubaki, T. (1980) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(80)90031-3 · Cited by 425
Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.
D'Azzo, A., Hoogeveen, A., Reuser, A. J., Robinson, D., & Galjaard, H. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.15.4535 · Cited by 365
The hereditary ataxias and related disorders
Harding, A. E. (1984) · Churchill Livingstone eBooks · Cited by 285
Sialidosis: a review of human neuraminidase deficiency.
Lowden, J. A., & O′Brien, J. S. (1979) · Europe PMC (PubMed Central) · Cited by 282
Cited by
Cellular and molecular basis of epilepsy
McNamara, J. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03413.1994 · Cited by 649
(2012) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52898-8.00004-5 · Cited by 40
Metadata
- Authors
- Berkovic, S. F., Andermann, F., Carpenter, S., & Wolfe, L. S.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 1986-07-31
- Volume
- 315
- Issue
- 5
- Pages
- 296-305
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W1973421354
- Cited by
- 310
- References
- 52
- FWCI
- 5.46
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Progressive Myoclonus Epilepsies: Specific Causes and Diagnosis. https://app.cochat.ai/papers/10.1056/nejm198607313150506
- The paper
- Berkovic, S. F., Andermann, F., Carpenter, S., & Wolfe, L. S. (1986). Progressive Myoclonus Epilepsies: Specific Causes and Diagnosis. New England Journal of Medicine. https://doi.org/10.1056/nejm198607313150506
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.
