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Nicolas Blanchard-Gutton Selected Research

Endplate Acetylcholinesterase Deficiency

1/2015A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome.

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Nicolas Blanchard-Gutton Research Topics

Disease

2Muscular Diseases (Myopathy)
06/2020 - 10/2015
2Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
07/2012 - 01/2012
1Disease Progression
01/2022
1Endplate Acetylcholinesterase Deficiency
01/2015
1Congenital Myasthenic Syndromes (Myasthenia Gravis, Congenital)
01/2015
1Cardiomyopathies (Cardiomyopathy)
07/2012
1Heart Failure
07/2012
1Hypertension (High Blood Pressure)
12/2009
1Renal Insufficiency (Renal Failure)
12/2009

Drug/Important Bio-Agent (IBA)

2BradykininIBA
07/2012 - 01/2012
1LipidsIBA
10/2015
1AcetylcholinesteraseIBA
01/2015
1CollagenIBA
01/2015
1Proteins (Proteins, Gene)FDA Link
07/2012
1DystrophinIBA
07/2012
1Nitric Oxide (Nitrogen Monoxide)FDA Link
01/2012
1MineralocorticoidsIBA
12/2009

Therapy/Procedure

1Investigational Therapies (Experimental Therapy)
01/2022
1Therapeutics
06/2020