Page last updated: 2024-08-26

glyoxal bis(2-hydroxyanil) and Congenital Myasthenia

glyoxal bis(2-hydroxyanil) has been researched along with Congenital Myasthenia in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chevessier, F; Girard, E; Krejci, E; McArdle, JJ; Mersdorf, U; Peter, C; Witzemann, V1
Gomez, CM; Groshong, JS; Maselli, RA; Verity, MA; Vohra, BP; Wollmann, RL1

Other Studies

2 other study(ies) available for glyoxal bis(2-hydroxyanil) and Congenital Myasthenia

ArticleYear
A new mouse model for the slow-channel congenital myasthenic syndrome induced by the AChR εL221F mutation.
    Neurobiology of disease, 2012, Volume: 45, Issue:3

    Topics: Acetylcholinesterase; Aminophenols; Animals; Biophysics; Diaphragm; Disease Models, Animal; Gene Expression Regulation; Genetic Predisposition to Disease; Hand Strength; Humans; In Vitro Techniques; Isoleucine; Mice; Mice, Transgenic; Microscopy, Electron, Transmission; Miniature Postsynaptic Potentials; Motor Endplate; Mutagenesis; Myasthenic Syndromes, Congenital; Neurofilament Proteins; Neuromuscular Junction; Patch-Clamp Techniques; Phenylalanine; Receptors, Nicotinic; S100 Proteins; Synaptophysin; Time Factors

2012
Focal caspase activation underlies the endplate myopathy in slow-channel syndrome.
    Annals of neurology, 2004, Volume: 55, Issue:3

    Topics: Age of Onset; Aminophenols; Apoptosis; Bungarotoxins; Calcium; Caspases; Cholinesterases; DNA Mutational Analysis; Enzyme Activation; Family Health; Humans; Immunohistochemistry; In Situ Nick-End Labeling; Microscopy, Electron; Motor Endplate; Muscles; Mutation; Myasthenic Syndromes, Congenital; Neurologic Examination; Oligodeoxyribonucleotides, Antisense; Protein Subunits; Receptors, Cholinergic

2004