Results 241 to 250 of about 18,132 (269)
Some of the next articles are maybe not open access.
Rinsho shinkeigaku = Clinical neurology, 2002
Recently, a variety of ion channel defects have been identified as the biological basis of certain familial epilepsies, paroxysmal movement disorders, myopathies and some degenerative disorders of central nervous system. Ion channel defects were mainly caused by genetic and autoimmune mechanisms.
K, Okamoto, Y, Ikeda
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Recently, a variety of ion channel defects have been identified as the biological basis of certain familial epilepsies, paroxysmal movement disorders, myopathies and some degenerative disorders of central nervous system. Ion channel defects were mainly caused by genetic and autoimmune mechanisms.
K, Okamoto, Y, Ikeda
openaire +1 more source
Pediatric neuromuscular channelopathies
Pediatric skeletal muscle channelopathies include a spectrum of conditions including nondystrophic myotonias and periodic paralyses. They are rare inherited conditions that can cause significant morbidity. They are characterized by episodic stiffness and weakness. While there is significant phenotypic variability, there are distinct diagnostic features.Vinojini, Vivekanandam +2 more
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Acquired Dendritic Channelopathy in Temporal Lobe Epilepsy
Science, 2004Christophe Bernard +2 more
exaly
Dravet syndrome—From epileptic encephalopathy to channelopathy
Epilepsia, 2014Andreas Brunklaus
exaly
A Novel Channelopathy in Pulmonary Arterial Hypertension
New England Journal of Medicine, 2013Danilo Roman-Campos +2 more
exaly
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder
Nature Genetics, 2005Huanghe Yang, Jianmin Cui, Qing K Wang
exaly