Publications by authors named "Stephen Cannon"

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The molecular transition that confers voltage dependence to muscle contraction.
Marina Angelini, Nicoletta Savalli, Federica Steccanella, Savana Maxfield, Serena Pozzi, Stephen C Cannon

Nat Commun· May 2025

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Potassium-sensitive loss of muscle force in the setting of reduced inward rectifier K current: Implications for Andersen-Tawil syndrome.
Nathaniel Elia, Marbella Quiñonez, Fenfen Wu, Ekaterina Mokhonova, Marino DiFranco, Stephen C Cannon

Proc Natl Acad Sci U S A· April 2025

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Periodic paralysis.
Stephen C Cannon

Handb Clin Neurol· August 2024

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Retigabine suppresses loss of force in mouse models of hypokalaemic periodic paralysis.
Marbella Quiñonez, Marino DiFranco, Fenfen Wu, Stephen C Cannon

Brain· April 2023

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Voltage-dependent Ca release is impaired in hypokalemic periodic paralysis caused by Ca1.1-R528H but not by Na1.4-R669H.
Marino DiFranco, Stephen C Cannon

Am J Physiol Cell Physiol· August 2022

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Gating pore currents occur in CaV1.1 domain III mutants associated with HypoPP.
Fenfen Wu, Marbella Quinonez, Stephen C Cannon

J Gen Physiol· November 2021

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The distinct role of the four voltage sensors of the skeletal CaV1.1 channel in voltage-dependent activation.
Nicoletta Savalli, Marina Angelini, Federica Steccanella, Julian Wier, Fenfen Wu, Stephen C Cannon

J Gen Physiol· November 2021

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Epilepsy channelopathies go neddy: stabilizing NaV1.1 channels by neddylation.
Stephen C Cannon

J Clin Invest· April 2021

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Guidelines on clinical presentation and management of nondystrophic myotonias.
Bas C Stunnenberg, Samantha LoRusso, W David Arnold, Richard J Barohn, Stephen C Cannon

Muscle Nerve· October 2020

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A role for external Ca2+ in maintaining muscle contractility in periodic paralysis.
Stephen C Cannon

J Gen Physiol· July 2020

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Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor.
Tomoya Kubota, Fenfen Wu, Savine Vicart, Maki Nakaza, Damien Sternberg, Stephen C Cannon

Brain Commun· July 2020

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Resurgent and Gating Pore Currents Induced by Epilepsy Mutations.
Emily R Mason, Fenfen Wu, Reesha R Patel, Yucheng Xiao, Stephen C Cannon

eNeuro· May 2020

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Further evidence for shared genetic susceptibility in both sporadic and Thyrotoxic periodic paralysis.
Stephen C Cannon

J Neurol Sci· May 2020

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Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in .
Nathaniel Elia, Trystan Nault, Hugh J McMillan, Gail E Graham, Lijia Huang, Stephen C Cannon

Front Neurol· March 2020

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Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L769V Mutation in .
Nathaniel Elia, Trystan Nault, Hugh J McMillan, Gail E Graham, Lijia Huang, Stephen C Cannon

Front Neurol· February 2020

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A highly-selective chloride microelectrode based on a mercuracarborand anion carrier.
Marino DiFranco, Marbella Quinonez, Rafal M Dziedzic, Alexander M Spokoyny, Stephen C Cannon

Sci Rep· December 2019

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A four-electrode method to study dynamics of ion activity and transport in skeletal muscle fibers.
Judith A Heiny, Stephen C Cannon, Marino DiFranco

J Gen Physiol· September 2019

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Recovery from acidosis is a robust trigger for loss of force in murine hypokalemic periodic paralysis.
Wentao Mi, Fenfen Wu, Marbella Quinonez, Marino DiFranco, Stephen C Cannon

J Gen Physiol· April 2019

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Myasthenic congenital myopathy from recessive mutations at a single residue in Na1.4.
Nathaniel Elia, Johanna Palmio, Marisol Sampedro Castañeda, Perry B Shieh, Marbella Quinonez, Stephen C Cannon

Neurology· March 2019

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[Intramural duodenal haematoma after endoscopic injection therapy of a bleeding ulcer].
Ditte Smed Iversen, Stephen Cannon, Ole K Bonderup

Ugeskr Laeger· September 2018

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Review of the Diagnosis and Treatment of Periodic Paralysis.
Jeffrey M Statland, Bertrand Fontaine, Michael G Hanna, Nicholas E Johnson, John T Kissel, Stephen C Cannon

Muscle Nerve· April 2018

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Kv4.2 autism and epilepsy mutation enhances inactivation of closed channels but impairs access to inactivated state after opening.
Meng-Chin A Lin, Stephen C Cannon, Diane M Papazian

Proc Natl Acad Sci U S A· April 2018

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Skeletal muscle channelopathy: a new risk for sudden infant death syndrome.
Stephen C Cannon

Lancet· April 2018

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Stac3 enhances expression of human Ca1.1 in oocytes and reveals gating pore currents in HypoPP mutant channels.
Fenfen Wu, Marbella Quinonez, Marino DiFranco, Stephen C Cannon

J Gen Physiol· March 2018

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An atypical Ca1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis.
Stephen C Cannon

J Gen Physiol· December 2017

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