The DOI matches its Crossref record; 117 of the 117 references it cites were found in a registry or an index.
Periodic paralysis
Abstract
The periodic paralyses are a group of skeletal muscle channelopathies characterizeed by intermittent attacks of muscle weakness often associated with altered serum potassium levels. The underlying genetic defects include mutations in genes encoding the skeletal muscle calcium channel Ca v 1.1, sodium channel Na v 1.4, and potassium channels K ir 2.1, K ir 3.4, and possibly K ir 2.6. Our increasing knowledge of how mutant channels affect muscle excitability has resulted in better understanding of many clinical phenomena which have been known for decades and sheds light on some of the factors that trigger attacks. Insights into the pathophysiology are also leading to new therapeutic approaches.
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“Unlike familial hypokalemic periodic paralysis, TPP can only happen during a hyperthyroid state [7].”
From A Case of Thyrotoxic Periodic Paralysis: "I Can't Move!" (2023) · cites this paper as [7]
Citations
Cites
From Ionic Currents to Molecular Mechanisms
Catterall, W. A. (2000) · Neuron · doi:10.1016/s0896-6273(00)81133-2 · Cited by 2,124
A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
Holt, I. J., Harding, A. E., Petty, R., & MORGAN-HUGHES, J. A. (1990) · PubMed · Cited by 1,004
K + Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension
Choi, M., Scholl, U. I., Yue, P., Björklund, P., Zhao, B., Nelson-Williams, C. J., Ji, W., Cho, Y., Patel, A. P., Men, C. J., et al. (2011) · Science · doi:10.1126/science.1198785 · Cited by 999
Plaster, N. M., Tawil, R., Tristani‐Firouzi, M., Canún, S., Bendahhou, S., Tsunoda, A., Donaldson, M. R., Iannaccone, S. T., Brunt, E. R. P., Barohn, R. J., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00342-7 · Cited by 993
Potassium channel block by cytoplasmic polyamines as the mechanism of intrinsic rectification
Lopatin, A. N., Makhina, E. N., & Nichols, C. G. (1994) · Nature · doi:10.1038/372366a0 · Cited by 855
Ohmic conductance through the inwardly rectifying K channel and blocking by internal Mg2+
Matsuda, H., Saigusa, A., & Irisawa, H. (1987) · Nature · doi:10.1038/325156a0 · Cited by 595
Na + -K + Pump Regulation and Skeletal Muscle Contractility
Clausen, T. (2003) · Physiological Reviews · doi:10.1152/physrev.00011.2003 · Cited by 582
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
Tristani‐Firouzi, M., Jensen, J. L., Donaldson, M. R., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15183 · Cited by 543
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
Ptáček, L. J. (1994) · Cell · doi:10.1016/0092-8674(94)90135-x · Cited by 426
A proton pore in a potassium channel voltage sensor reveals a focused electric field
Starace, D. M., & Bezanilla, F. (2004) · Nature · doi:10.1038/nature02270 · Cited by 401
Flagged first, then by citations
Research works printed but not linked: 2
- Kuhn, 2016, Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients, J Neurol Neurosurg Psychiatry, 87, 49
- Rosenfeld, 1902, Akute aufsteigende Lähmung bei Morbus Basedow. Berl, klin Wochenschr, 39, 538
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Regulation of muscle potassium: exercise performance, fatigue and health implications
Lindinger, M. I., & Cairns, S. P. (2021) · European Journal of Applied Physiology · doi:10.1007/s00421-020-04546-8 · Cited by 78
Periodic Paralysis: A Case Series with a Literature Review
Al Hariri, B., Hassan, M. A., Sharif, M., Alsakaji, O. A., Hassan, Y. A., & Khalid, M. K. (2024) · Case Reports in Neurology · doi:10.1159/000541585 · Cited by 8
A Case of Thyrotoxic Periodic Paralysis: "I Can't Move!"
Basnet, A., Goyal, N., Tiwari, K., Kansakar, S., & Gautam, S. (2023) · Cureus · doi:10.7759/cureus.34301 · Cited by 2
Metadata
- Authors
- Fialho, D., Griggs, R. C., & Matthews, E. L.
- Affiliations
- National Hospital for Neurology and Neurosurgery (GB)
- University of Rochester Medicine (US)
- Corresponding author
- Robert C. Griggs
- Venue
- Handbook of clinical neurology
- Publisher
- Elsevier
- Published
- 2018
- Volume
- 148
- Pages
- 505-520
- ISSN
- 0072-9752 (ISSN-L)
- OpenAlex
- W4211027566
- Cited by
- 61
- References
- 117
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 10 · 2023: 9 · 2022: 9 · 2021: 7 · 2020: 7 · 2019: 4 · 2018: 4
- FWCI
- 7.41
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Handbook of clinical neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- periodic paralysis, skeletal muscle channelopathies, muscle weakness, serum potassium, CaV1.1, Nav1.4, Kir2.1, Kir3.4, muscle excitability, pathophysiology, treatment
- MeSH terms
- Humans, Ion Channels, Mutation, Paralyses, Familial Periodic, Genetic Predisposition to Disease
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