Cargando…
Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy: A Case Report With Critical Therapeutical Implications and Review of the Literature
Skeletal muscle sodium channelopathies are a group of neuromuscular disorders associated with mutations in the SCN4A gene. Because principal sodium channel isoforms expressed in the skeletal muscles and the heart are distinct one from the other, this condition usually spares cardiac functioning. Non...
Autores principales: | Cavalli, Michele, Fossati, Barbara, Vitale, Raffaele, Brigonzi, Elisa, Ricigliano, Vito A. G., Saraceno, Lorenzo, Cardani, Rosanna, Pappone, Carlo, Meola, Giovanni |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988887/ https://www.ncbi.nlm.nih.gov/pubmed/29899727 http://dx.doi.org/10.3389/fneur.2018.00385 |
Ejemplares similares
-
Neuropsychological and Psychological Functioning Aspects in Myotonic Dystrophy Type 1 Patients in Italy
por: Callus, Edward, et al.
Publicado: (2018) -
Aberrant insulin receptor expression is associated with insulin resistance and skeletal muscle atrophy in myotonic dystrophies
por: Renna, Laura Valentina, et al.
Publicado: (2019) -
Sporadic MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis
por: Saraceno, Lorenzo, et al.
Publicado: (2018) -
MSA Mimic? Rare Occurrence of Anti-Hu Autonomic Failure and Thymoma in a Patient with Parkinsonism: Case Report and Literature Review
por: Ricigliano, Vito A. G., et al.
Publicado: (2018) -
Editorial: New Insights in Skeletal Muscle Channelopathies - A Rapidly Expanding Field
por: Maggi, Lorenzo, et al.
Publicado: (2020)