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Journal of Clinical Neuromuscular Disease|August 28, 2019
Phenotypic Differences in 2 Unrelated Cases Carrying Identical DOK7 MutationsVéronique Bissay, Ricardo A MaselliActa Clinica Belgica|November 2, 2017
What the internist should know about hereditary muscle channelopathiesVéronique Bissay, Sophie C H Van MalderenMuscle & Nerve|November 18, 2008
Fatigue as the presenting symptom of chronic inflammatory demyelinating polyneuropathyVéronique Bissay, Anja Flamez, Eric Schmedding, et al.Journal of the Neurological Sciences|July 15, 2011
A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperatureVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.Neuromuscular Disorders : NMD|June 14, 2011
Late onset painful cold-aggravated myotonia: three families with SCN4A L1436P mutationVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.Acta Neurologica Belgica|September 3, 2021
SARS-CoV-2-associated Guillain-Barré syndrome in four patients: what do we know about pathophysiology?Antoine Guilmot, Sofia Maldonado Slootjes, Véronique Bissay, et al.Frontiers in Neurology|October 10, 2022
Case report: Coexistence of myotonia congenita and Brugada syndrome in one familyAnn Cordenier, Anja Flamez, Thomy de Ravel, et al.Acta Neurologica Belgica|April 22, 2024
Recommendations for the management of myasthenia gravis in BelgiumJan L De Bleecker, Gauthier Remiche, Alicia Alonso-Jiménez, et al.European Journal of Human Genetics : EJHG|June 4, 2015
SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathiesVéronique Bissay, Sophie C H Van Malderen, Kathelijn Keymolen, et al.The International Journal of Cardiovascular Imaging|December 5, 2022
Prognostic value of left ventricular global constructive work in patients with cardiac amyloidosisJolien Geers, Maria-Luiza Luchian, Andreea Motoc, et al.Pageof 2